CN1420783A

CN1420783A - Compositions and methods for tumor-targeted delivery of effector molecules

Info

Publication number: CN1420783A
Application number: CN00816714A
Authority: CN
Inventors: D·G·贝尔穆德斯; I·C·金; C·A·克莱尔蒙特; S·L·林; M·贝尔库特
Original assignee: Vion Pharmaceuticals Inc
Current assignee: Vion Pharmaceuticals Inc
Priority date: 1999-10-04
Filing date: 2000-08-24
Publication date: 2003-05-28
Also published as: EP1261369A2; NZ518354A; AU783714B2; CA2386465A1; BR0014491A; WO2001025397A2; KR20020059605A; MXPA02003384A; AU6933400A; JP2004500042A; IL148933A0; WO2001025397A3; EP1261369A4

Abstract

The present application discloses the preparation and use of attenuated tumor-targeted bacteria vectors for the delivery of one or more primary effector molecule(s) to the site of a solid tumor. The primary effector molecule(s) of the invention is used in the methods of the invention to treat a solid tumor cancer such as a carcinoma, melanoma, lymphoma, or sarcoma. The invention relates to the surprising discovery that effector molecules, which may be toxic when administered systemically to a host, can be delivered locally to tumors by attenuated tumor-targeted bacteria with reduced toxicity to the host. The application also discloses the delivery of one or more optional effector molecule(s) (termed secondary effector molecules) which may be delivered by the attenuated tumor-targeted bacteria in conjunction with the primary effector molecule(s).

Description

Be used for compositions and the method for effector molecule targeted delivery to tumor

The application requires the U.S. Provisional Patent Application 60/157,500,60/157,581 of submission on October 4th, 1999 and 60/157,637 priority, and its content separately is all in this comprehensive introducing, as a reference.

1. Invention field

The present invention relates to one or more primary effector molecules are delivered to solid tumor, be used for the treatment of or suppress this tumor.More particularly, the present invention relates to be oriented to the preparation and the purposes of the attenuated bacteria of tumor, it is delivered to suitable site of action to one or more primary effector molecules as carrier, as the solid tumor position such as Salmonella etc.In detail, the attenuated bacteria that is oriented to tumor of the present invention is through modifying the facultative aerobe or the facultative anaerobe of one or more primary effector molecules of codified.Primary effector molecule of the present invention comprises member, anti-angiogenesis and the cytotoxicity polypeptide or the peptide of TNF cytokine family.Primary effector molecule of the present invention can be used to, for example, and treatment cancer, melanoma, lymphoma, sarcoma or derive from the solid tumors such as metastasis of these tumors.The invention still further relates to a surprising discovery, promptly utilize be oriented to tumor and to the less attenuated bacteria of host's toxicity immunologic complication lower, that cause can with such as TNF family member, anti-angiogenesis and primary effector molecule local deliveries such as cytotoxicity polypeptide or peptide to tumor.The invention still further relates to one or more optional effector molecules delivering method of (being called " second order effect molecule "), the attenuated bacteria that these effector molecules can be by being oriented to tumor and primary effector molecule is collaborative sends.The second order effect molecule provides extra antineoplaston activity, promotes the attenuated bacteria be oriented to tumor to discharge primary effector molecule, and (perhaps) strengthen solid tumor position etc. suitably site of action to the picked-up of primary effector molecule.

2. Background of invention

Vegetation, or tumor are a kind of superfluous natural disposition agglomerates that is produced by abnormal growth of cells, and it can be benign, also can be virulent.Benign tumor generally can maintain the part.Contiguous bodily tissue might be attacked and destroy to malignant tumor usually, and can be diffused into distal site and cause death (about the summary, can be with reference to Robins and Angel, 1976, BasicPathology, 2d Ed., W.B.Saunders Co., Philadelphia, pp.68-122).Transfer has taken place when tumor is called as when a kind of organ or tissue is diffused into another kind of organ or tissue.

A main difficult problem of solid tumor being carried out chemotherapy is the concentration of treatment agent of sending, as the drug level of sending, and be enough to eradicate tumor cell, reduces Normocellular infringement again simultaneously as far as possible.Therefore, it is the biological delivery systems of design that many breadboard research directions are arranged, for example, be used for medicine, prodrug invertase and (or) gene targeted delivery to antibody, cytokine and the virus of tumor cell (can reference, for example, Crystal, R.G., 1995, Science270:404-410).2.1. Cellular immunization and cytokine

Having a kind of strategy for the treatment of cancer to relate to strengthens or the active cell immunne response.Compare with traditional embolic chemotherapy, successfully induce a kind of method of the cellullar immunologic response at autologous tumor to have several advantages: 1) immunity identification has high degree of specificity, and it can be specially at tumor; 2) can suppress the growth of metastasis site by immune surveillance; 3) immunne response and the multiformity of immunity identification can remedy the different resistance mechanisms of tumor cell; 4) the cytotoxic T cell clone can expand sooner than tumor, makes antitumor mechanism can finally defeat tumor; And 5) before carrying out physical examination, memory response can be suppressed at palindromia the earliest period stage.The The Animal Model Study result is supported in the clinical research of replying patient, though it shows the participation that CD4+T cell, macrophage and NK cell are described on evidence, but successful immunotherapy relates to activation CD8+T cell (the I class is replied), and response patient's clinical research has also been proved this result.Can reference, for example, Chapoval et al., 1998, J.Immunol.161:6977-6984; Gollubet al., 1998, J.Clin.Invest.102:561-575; Kikuchi et al., 1999, Int.J.Cancer 80:425-430; Pan et al., 1995, Int.J.Cancer 80:425-430; Saffran et al., 1998, Cancer Gene Ther.5:321-330; And Zimmermann et al., 1999, Eur.J.Immunol.29:284-290.2.2. The tumor necrosis factor of cytokine (TNF) family

It is TNF-α that character is understood the TNF family member who removes most.Known TNF-α can produce many-sided influence to immune system.TNF-α is a kind of cytokine that can directly produce strong cytotoxic effect to tumor cell.It has been generally acknowledged that TNF-α can be by other its antitumor actions of mechanism performance, for example stimulate proliferation and break up, stop the mononuclear cell apoptosis (can reference, for example, Mangan et al., 1991, J.Immunol.146:1541-1546; With Ostensenet al., 1987, J.Immunol.138:4185-4191), improve tissue factor sample procoagulant activity, and inhibition endothelial cell surface anticoagulating active, thereby finally cause forming in the tumor blood clot (see Beutler and Cerami, 1989, Ann.Rev.Immunol.7:625-655; And Vassalli, P., 1992, the summary of Ann.Rev.Immunol.10:411-452).But if the result of these characteristics is with the administration of TNF-α whole body, can cause the host because of the lethal consequence of disseminated inravascular coagulation.

Antitumor is replied and has also been related to other cytokines.IL-2 belongs to the I type cytokines, and it is considered to play a part in antitumor is replied certain.For example, melanomatous spontaneous regression is relevant with the increase of interior TNF-α of tumor and IL-2 level.Can reference, for example, Beutler andCerami, 1989, Annu.Rev.Immunol.7:625-655; Lowes et al., 1997, J.Invest.Dermatol.108:914-919; Mangan et al., 1991, J.Immunol.146:1541-1546; Scheruich et al., 1987, J.Immunol.138:1786-1790.

TNF-α and IL-2 help lymphocyte homing, and proved that but the IL-2 inducing natural kills and wounds (NK) cell, T cell and lymphokine is activated and killed and wounded (LAK) cell to the infiltration of tumor (can reference, for example, Etter et al., 1998, Cytokine 10:395-403; Reinhardt et al., 1997, Blood 89:3837-46; Chen et al., 1997, J.Neurophathol.Exp.Neurol.56:541-50; Vora et al., 1996, Clin.Exp.Immunol.105:155-62; Luscinskas et al., 1996, J.Immunol.157:326-35; Kjaergaard et al., 1998, Scand.J.Immunol.47,532-540; Johansson et al., 1996, Nat.Immun.15:87-97; With Watanabe et al., 1997, Am.J.Pathol.150:1869-80).When TNF-α and IL-2 existed, the dissolved cell activity of NK and LAK cell all improved, in addition to the dissolved cell activity of the insensitive cell line of TNF-also increase (reference, for example, Ostensen et al., 1987, J.Immunol.138:4185-4191).But the IL-2 of treatment level also shows the toxicity to the host.

Cytokine whole body administration meeting is produced the toxic action that is subjected to dose limitation, and this is undoubtedly for realizing that the effect of cytokine in treatment of cancer is provided with together significantly obstacle.In addition, cytokine whole body administration meeting is reduced the targetting of homology T cell, and resist directed immunization therapy thus, also can cause deleterious clinical side effects in addition.With reference to Addison et al., 1998, Gene Ther.5:1400-1409; Albertini et al., 1997, Clin.CancerRes.3:1277-1288; Becker et al., 1996, Proc.Natl.Acad.Sci.USA93:7826-7831; Book et al., 1998, J.Neuroimmunol.92:50-59; Cao et al., 1998, J.Cancer Res.Clin Oncol.124:88-92; D ' Angelica et al., 1999, Cancer Immunol.Immunother.47:265-271; Deszo et al., 1996, Clin.Cancer Res.2:1543-1552; Kjaergaard et al., 1998, Scand.J.Immunol.47:532-540; Ostensen et al., 1987, J.Immunol.138:4185-4191; With Schirrmacher et al., 1998, Clin.Cancer Res.4:2635-2645.2.3. Sending of cytokine

Recent laboratory animal research and clinical research are attempted to avoid the general toxicity of cytokine and more high dose administration by the inferior whole body administration of cytokine or other method.In mouse model, treat the S-180 tumor by the TNF-α gene drug delivery method of gene fusion liposome with the TNF-α whole body medication of the Polyethylene Glycol parcel that can be confined to the tumor vessel system at present and (see Tsutsumi et al., 1996, Jpn.J.Cancer Res.87:1078-1085).Also reported in addition endothelium-mononuclear cell-activating peptide II can promote tumor to the sensitivity of TNF-α (see Marvin et al., 1999, J.Surg.Res.63:248-255; Wuet al., 1996, Cancer Res.59:205-212).

Clinical research finds, with isolation limbs method for filling the TNF-α of high dose and interferon-alpha or melphalan combination medicine-feeding can be eradicated tumor fully in the patient.But if fail to remove fully cytokine after treatment, this technology will be brought very serious risk for the patient.In addition, these processing method limbs are isolated, and this itself will bring danger for the patient.Can be with reference to Eggermont et al., 1997, Semin.Oncol.24:547-555; Fraker etal., 1995, Cancer J.Sci.Am.1:122-130; Lejeune et al., 1998, Curr.Opin.Immunol.10:573-580; Marvin et al., 1996, J.Surg.Res.63:248-255; Mizuguchi et al., 1998, Cancer Res.58:5725-5730; Tsutsumi et al., 1996, Jpn.J.Cancer Res.87:1078-1085; With Wu et al., 1996, Cancer Res.59:205-212.

According to Carrier et al. before this, 1992, J.Immunol.148:1176-81; Saltzman et al., 1997, Cancer Biother.Radiopharm.12:37-45; Saltzman et al., 1997, the result of study that J.Pediat.Surgery 32:301-306 delivers, can utilize the Salmonella attenuated strain directly IL-1 β (Carrier) and IL-2 (Saltzman) to be delivered to the natural infection position of Salmonella, liver and spleen, thus serve as vaccine strains or influence the metastasis (metastases) of liver.The method of Salmonella oral administration is adopted in the research of Saltzman, and this method is to absorb antibacterial and it is transported to liver and spleen with GALT (gut associated lymphoid tissue).But these infection are confined to the natural infection position.2.4. Blood vessel takes place to take place with tumor

Another kind of strategy of cancer treatment relates to blood vessel is suppressed.Blood vessel is meant that original blood vessel grows the process of new blood capillary.The forming process of new blood capillary is, the endotheliocyte of original blood vessel utilizes Proteolytic enzyme enzymatic degradation such as matrix metalloproteinase basement membrane around it, and propagation is in the matrix organization around moving to and form microchannel.The blood vessel generating process is subjected to the interactional tight regulation and control between the negative factor and the positive divisor, and this process generally is only limited to female reproduction cycle and wound repair (Malonne et al., 1999, Clin.Exp.Metastasis 17:1-14) in the adult.Have that multiple human diseases and blood vessel take place wrong or regulate and control unusually relevant, comprising diabetic retinopathy, psoriasis, rheumatoid arthritis, cardiovascular disease and tumor take place (Folkman, 1995, Nat.Med.1:27-31).

The blood vessel generating process is to growth of tumor and shift most important.Tumor forms can be divided into two stages, i.e. blood vessel early stage and blood vessel phase.Studies show that blood vessel early stage, tumor cell can resemble fast breeding the blood vessel phase tumor cell.But blood vessel tumor in early stage seldom grows into 2-3mm ³More than because exist between the cell death that the low oxygen characteristic of cell proliferation and blood vessel tumor in early stage causes a kind of balance (Folkman, 1995, Nat.Med.1:27-31).Blood vessel changes the balance change that the blood vessel phase needs blood vessel generation regulatory factor in earlier stage into, from the negative dominant clean balance change of the factor is positive divisor, as fibroblast growth factor (FGF) and the dominant clean balance (Cao of vascular endothelial cell growth factor (VEGF), 1998, Prog.Mol.Subcell.Biol.20:161-176).This equilibrated transformation between the regulatory factor is to raise angiogenesis factor, reduce simultaneously anti-angiogenesis the result (Folkman, 1995, N.Eng.J.Med.333:1757-1763).2.5. Anti-angiogenesis

Infer that the foundation that anti-angiogenesis exists is, judge from some correlated phenomena, primary tumor can suppress usually its metastasis growth (Cao, 1998, Prog.Mol.Subcell.Biol.20:161-176).In these factors, what at first separate is the mice angiostatin, it is a kind of 38kDa proteolytic fragments that constitutional Lewis lung cancer tumor is discharged into the plasminogen in the blood circulation, this fragment can hinder the secondary metastasis growth (O ' Reilly et al., 1994, Cell 79:315-328).In the mankind, the peptide of 40,42 and the 45kDa that the limited hydrolysis of plasminogen is produced by metalloelastase has and the similar anti-angiogenesis activity of mice angiostatin (O ' Reilly et al., 1994, Cell 79:315-328).Plasminogen itself does not have this activity.Think also that in addition tumor-associated macrophages can produce angiostatin, because tumor cell itself does not contain detectable angiostatin mRNA.The granulocyte colony-stimulating factor of tumor cell secretion (GM-CSF) can induce macrophage express metalloelastase (Dong et al., 1997, Cell88:80-810).In some tumor the generation that comes the catalysis angiostatin by the serine protease that tumor cell directly produces, rather than metalloelastase (Gately et al., 1997, Cancer Res.56:4887-4890).With 100mg/kg/ days concentration angiostatin is delivered medicine to the test mice of suffering from primary tumor, then can under the condition of not toxigenicity side effect, produce intensive inhibition tumor growth.Tumor can regrow in 2 weeks after the angiostatin therapy stops, and shows that this therapy can cause tumour regression to resting state, rather than dead fully (O ' Reilly et al., 1996, Nat.Med.2:689-692).

After finding angiostatin, find again and separated some other angiogenesis inhibitor, comprising several angiogenesis inhibitory peptides.Kringle 5 is a kind of than the more effective angiogenesis inhibitor of angiostatin, it is a kind of peptide (angiostatin contains the 1-4kringle domain) that contains plasminogen 5kringle domain, its recombinant forms has activity (Cao et al. equally, 1997, J.Biol.Chem.272:22924-22928).

The separate mode and the angiostatin of interior chalone (endostatin) similar (O ' Reilly etal., 1997, Cell 88:1-20), its source is the Mus hemangioendothelioma, rather than Lewis lung cancer.The apparent molecular weight of this peptide is 20kDa, its sequence be equivalent to the C-end regions that a section of collagen protein XVIII is called NCl (O ' Reilly et al., 1997, Cell88:1-20), this zone (Oh et al. that in different collagen molecules, alters a great deal, 1994, Proc.Natl.Acad.Sci.USA 91:4229-4233; With Rehn et al., 1994, Proc.Natl.Acad.Sci.USA 91:4234-4239).In mice, the chalone administration can suppress the growth of Lewis lung cancer metastasis in will recombinating with 0.3mg/kg/ days concentration, then can make primary tumor degenerate to resting state with 20mg/kg/ days concentration administrations.Chalone can be produced by inclusion body by external degeneration and refolding in the functional reorganization, discharge in the durative of interior chalone inclusion body preparation that also can be by subcutaneous administration and produce (O ' Reilly et al., 1997, Cell 88:1-20).As the alternative method of chalone in sending, the expression plasmid of interior chalone can also be carried out intramuscular administration, this method in mouse model system, can only partly suppress tumor growth (Blezinger et al., 1999, Nat.Biotech.17:343-348).Similarly, with liposome compound in chalone or the angiotensin coding plasmid delivering method that carries out intravenous administration can partly suppress tumor growth (Chen etal., 1999, Cancer Res.59:3308-3312) in the breast carcinoma nude mice model.

Recent findings, a kind of C end truncated peptide of Serpin (serpin) antithrombase have new anti-angiogenesis activity (O ' Reilly et al., 1999, Science285:1926-1928).The antithrombase of total length is not the congenital anti-angiogenesis activity that has, and is sheared by thrombin but the active ring of its C end is distinguished, and antithrombase can obtain very strong angiogenic activity.Hereinafter will call the angiogenesis inhibitor antithrombase to this proteolytic fragments.

Other angiogenesis inhibitory peptides known in the art comprise, and the C end protein hydrolysis fragment of the N end protein hydrolysis fragment of a kind of 29kDa of fibronectin and a kind of 40kDa (Homandberg et al., 1985, J.Am.Pathol.120:327-332); The proteolytic fragments of a kind of 16kDa of prolactin antagonist (Clapp et al., 1993, Endocrinology 133:1292-1299); The proteolytic fragments of a kind of 7.8kDa of PF4 (Gupta et al., 1995, Proc.Natl.Acad.Sci.USA92:7799-7803).

Except those have proved the proteolytic fragments of the natural generation with blood vessel formation against function, some synthetic peptides that are equivalent to known extracellular matrix protein specific region have also been carried out the evaluation of angiogenesis inhibiting activity.Proved the synthetic peptide that can be used as functional endotheliocyte inhibitor, promptly, comprise, be equivalent to segmental a kind of 13 amino acid whose peptides (Maione et al. of PF4 as the synthetic peptide of angiogenesis inhibitor, 1990, Cancer Res.51:2077-2083); Segmental a kind of 14 the amino acid whose peptides (Tolsma et al., 1993, J.Cell Biol.122:497-511) that are equivalent to collagen protein I; Segmental a kind of 19 the amino acid whose peptides (Tolsma et al., 1993, J.Cell Biol.122:497-511) that are equivalent to thrombospondin I; And segmental a kind of 20 amino acid whose peptides (the Sage et al. that is equivalent to SPARC, 1995, J.Cell.Biochem.57:1329-1334), this is a kind of excretory extracellular matrix glycoprotein that is rich in cysteine, the expression of this glycoprotein in human melanoma cell can cause the minimizing of cell in vitro invasion and attack, and in the nude mice model body, can cause the tumor generating ability to reduce (Ledda et al., 1996, Nature Med.3:171-176).Some other peptide that is less than 10 amino acid residues that suppresses angiogenesis has also been described in addition, these peptides are equivalent to the fragment of laminin, fibronectin, precollagen and EGF respectively and (see Cao, 1998, the summary of Prog.Mol.Subcell.Biol.20:161-176).

The fibronectin small-molecular peptides that can suppress angiogenesis generally all contains the RGD motif.RGD is a kind of peptide motif (an Arg-Gly-Asp aminoacid), and albumen can be by this motif identification and integrin binding molecule.The angiogenic blood vessel is all with beta 2 integrin alpha _vβ ₃Expression, suppress this proteic activity vascularization capable of blocking (Brooks et al., 1994, Science 264:569-571) with monoclonal antibody.This point be studied confirm, this studies show that the ring pentapeptide that contains the RGD motif can suppress the activity of Vitronectic receptor type integrin, and amphiblestroid neovascularization capable of blocking (Hammes et al., 1996, Nature Medicine2:529-533).The integrin blocker as ring pentapeptide and monoclonal antibody, has blood vessel formation against function, and this effect can be induced the apoptosis of angiogenic blood vessel, promotes tumour regression (Brooks et al., 1994, Cell 79:1157-1164) with this.The peptide that contains RGD motif and another kind of integrain binding motif NGR (Asn-Gln-Arg aminoacid) can show obvious enhanced anti-tumor activity.

By suppressing the activity of another kind of cell surface receptor, promptly suppress the activity of urokinase plasminogen activator (uPA) receptor, also can produce inhibitory action to angiogenesis.In a single day the uPA receptor combines with part, can cause a kind of Proteolytic enzyme cascade reaction, and this cascade reaction is that basement membrane invasion and attack step is necessary in the angiogenesis.But suppress the generation of uPA receptor line artery, tumor growth (Min et al., 1996, Cancer Res.56:2428-2433) and shift (Crowley et al., 1993, Proc.Natl.Acad.Sci.USA 90:5021-5025) with receptor antagonist.Utilize at random the phage display peptide display technique of peptide identified some such antagonisies (Goodson et al., Proc.Natl.Acad.Sci.USA91:7129-7133).Also identified the receptors ligand uPA (Minet al., 1996, Cancer Res.56:2428-2433) of dominant form in addition.

The treatment of cancer that is found to be of angiostatin, interior chalone and other anti-angiogenic peptides provides a kind of infusive new method, but, also impracticable with the method that one or more these peptides are treated, because this need produce a large amount of peptides (with the general artificial example of 65kg or 143lbs, need produce about 1.3 or 6.5g albumen every day, from its cost and (or) labour that drops into consider very unrealistic), from persistent period of treatment also be so (if will keep the degenerate state of tumor, must SM).These peptides must heavy dose of administration like this reason mainly contain 2 points, the first, most of peptide is degraded in blood flow, the second, in the molecule that is not degraded, have only a very limited part can arrive tumor.Therefore, if can will bring very large interests for the oncotherapy field more to save cost and more friendly mode more effectively is delivered to tumor with anti-angiogenic proteins or peptide.2.6. Bacteriocin family

Colicine E3 (after this being called ColE3) is a kind of bacteriocin, promptly has the bacterial protein toxin of selective active, because its host is to this toxin immunity.Bacteriocin can be by host genome or plasmid-encoded, its host range can be wide can be narrow, bacteriocin can be the simple structure that only contains one or two subunit, also can be many subunit structures (Konisky, 1982, Ann.Rev.Microbiol.36:125-144).In addition, the host of bacteriocin has the immunity of this bacteriocin of opposing.This immunity can appear in all cells of specific host colony, even appears at the cell of not expressing this bacteriocin.

The cytotoxicity of ColE3 derives from it to the synthetic inhibition of albumen (Nomura, 1963, Cold Spring Harbor Symp.Quant.Biol.28:315-324).The active effective object of ColE3 is the 16S component of bacterial ribosome, 30S and 70S ribosome all contain this component (Bowman et al., 1971, Proc.Natl.Acad.Sci.USA.68:964-968), this activity can cause ribosome degraded (Meyhack, 1970, Proc.Natl.Acad.Sci.USA).In the RNA enzyme, the activity of ColE3 is very unique, because it can not cause RNA all to degrade, but only shears 49 nucleotide of end of mRNA molecule, so that rRNA separates with mRNA, and suppresses translation thus.ColE3 residue in the molecule itself promptly has ribonuclease activity, does not need another kind of albumen to mediate (Saunders, 1978, Nature 274:113-114).ColE3 can also pass inner membrance and the adventitia of target cell.

The ColE3 of native form is the albumen composition of a kind of 60kDa, is that 1: 1 a kind of 50kDa albumen and a kind of 10kDa albumen is formed by ratio, and bigger subunit has nuclease, and less subunit has the function that suppresses the 50kDa subunit.Therefore, the albumen of 50kDa can be used as a kind of cytotoxic protein (or toxin), and the albumen of 10kDa can be used as a kind of antitoxin.The subunit of 50kDa contains two kinds of functional domains at least, promptly passes through the necessary N-end regions of target cell membrane and has the active C-end regions of catalysis (RNA enzyme).In host living beings, the activity of big subunit is suppressed by small subunit.In case this toxin enters target cell, then can make subunit dissociation (see Konisky, 1982, the summary of Ann.Rev.Microbiol.36:125-144) by interaction with the target cell adventitia.

The toxicity of the big subunit of ColE3 has been used to hinder the lateral diffusion of clone gene in microorganism.People such as Diaz (1994, Mol.Microbiol.13:855-861) separated these two kinds of components of ColE3, make the formal representation of little (mithridatism) subunit with the chromosomal integration coded sequence, big subunit is then by plasmid expression.The antibacterial that has the chromosomal integration small subunit is to expressing the plasmid immunity of the big subunit of ColE3, and still if this plasmid side direction is transferred to the cell of accepting that another does not contain small subunit, this cell will be killed.

The degree of depth cytotoxic effect that colicine E3 (ColE3) also can show mammalian cell (is seen Smarda et al., 1978, Folia Microbiol.23:272-277), (see Fiska et al. comprising degree of depth cytotoxic effect to a kind of leukaemia's model system, 1979, Experimentia 35:406-407).The active effective object of ColE3 be the ribosomal 40S subunit of mammal 80S (Turnowsky et al., 1973, Biochem.Biophys.Res.Comm.52:327-334).2.7. Bacterial infection and cancer

Reported some cases in the clinic observation in early days, promptly degeneration has appearred in the more intravital cancers of bacterial infection patient, sees Nauts et al., and 1953, Acta Medica.Scandinavica 145:1-102, (Suppl.276); And Shear, 1950, J.A.M.A.142:383-390.After this, Lee et al., 1992, Proc.Natl.Acad.Sci.USA 89:1847-1851 (people such as Lee) and Jones et al., 1992, Infect.Immun.60:2475-2480 people such as () Jones isolates some Salmonella typhimurium mutants, and these mutants are compared with wild-type strain, can have obviously more thalline to invade HEp-2 (people's epidermoid carcinoma) cell that exsomatizes.These " high aggressive " mutants are to separate to obtain under the condition that is fit to the aerobe growth, and this condition can suppress the invasive ability of wild-type strain to the HEp-2 zooblast usually.But the high aggressive Salmonella typhimurium that people such as people such as Lee and Jones describe has the danger that causes general aggressive to infect, and can cause bacterial infection widely in cancer patient's body.

Carswell et al., 1975, Proc.Natl.Acad.Sci.USA72:3666-3669 confirms, in the mice of injection of BCG vaccine (BCG), the TNF content of serum increases, and the TNF positive serum can cause the intravital Meth A of mice sarcoma and other transplantation tumors necrosis to occur.Just because of these observed results, still in some modality of cancer treatment, inject at present the cancer patient is carried out immunity by BCG.The summary of relevant BCG therapy is seen Sosnowski, 1994, and Compr.Ther.20:695-701; Barth and Morton, 1995, Cancer75 (Suppl.2): 726-734; Friberg, 1993, Med.Oncol.Tumor.Pharmacother.10:31-36.

But, use antibacterial can cause people's worry, the alpha mediated septic shock of TNF-is exactly one of main worry, and it can be to host's toxigenicity, or brings lethal consequence (Bone, 1992, JAMA 268:3452-3455; Dinarello et al., 1993, JAMA269:1829-1835).In addition, TNF-α can produce the general toxicity that is subjected to dose limitation, and this also becomes the major obstacle of its effective clinical practice.It is useful modifying to reduce this immunne response because TNF-alpha levels in this case can toxigenicity, so can adopt more effective treatment carrier concn and (or) course of treatment.2.8. Be oriented to the antibacterial of tumor

Proved that the genetic engineering Salmonella may be directed to tumor, and had anti-tumor activity, can be used for sending the gene (Pawelek et al., WO 96/40238) of herpes simplex virus thymidine kinase effector agents such as (KSV TK) effectively to solid tumor.2.9. The antibacterial lipid A of modifying causes the reduction of inducing to TNF-α

People such as Pawelek suggestion is modified the lipid component of the antibacterial that is oriented to tumor, with by the inductive reduction that produces TNF α is changed immunne response (Pawelek et al., WO96/40238).People such as Pawelek provide certain methods, are used for separating those from red bacillus and are responsible for producing the gene of monophosphoryl lipid A (MLA).MLA can be used as a kind of antagonist of septic shock.People such as Pawelek also advise the biosynthesis pathway of lipid A is carried out genetic modification; sudden change comprising the firA gene; the third enzyme in this gene codified lipid A biosynthesis pathway; be UDP-3-O (R-30 hydroxyl nutmeg acyl)-glycosamine-acyltransferase (Kelley et al.; 1993, J.Biol.Chem.268:19866-19874).People such as Pawelek point out that lower TNF alpha levels is induced in the sudden change of firA gene.

MsbB (mlt) gene (Engel, et al., 1992, the J.Bacteriol.174:6394-6403 of the terminal nutmeg acidylate of a kind of responsible lipid A in escherichia coli, have been identified; Karow and Georgopoulos 1992, J.Bacteriol.174:702-710; Somerville et al., 1996, J.Clin.Invest.97:359-365).This gene is carried out hereditary destruction can produce a kind of stable unconditionality sudden change, this sudden change can reduce the inducing action of TNF α (Somerville et al., 1996, J.Clin.Inyest.97:359-365; Somerville WO97/25061).But these lists of references do not propose, and the msbB gene that destroys in the Salmonella carrier that is oriented to tumor can make the toxicity of antibacterial reduce, and makes antibacterial more responsive to chelating agen.

Involve some problems with antibacterial as gene delivery vector, mainly be that antibacterial can directly kill normal mammalian cell usually, and can be by can be to the toxigenous TNF α of host and overstimulation immune system (Bone, 1992, JAMA 268:3452-3455; With Dinarello et al., 1993, JAMA 269:1829-1835).Except these factors, can make in the human body existence of antibacterial become very complicated (Tschape, 1996, D T W Dtsch Tierarztl Wochenschr 1996103:273-7 to antibiotic resistance; Ramos et al., 1996, Enferm Infec.Microbiol.Clin.14:345-51).

Hone and Powell, WO97/18837 (" Hone and Powell ") discloses certain methods, is used to produce the gram negative bacteria that contains nonthermal source lipid A or LPS.

Maskell, WO98/33923 have described a kind of mutant salmonella bacterial strain that contains a sudden change in the msbB gene, and this bacterial strain is compared the TNF α that can induce reduced levels with wild-type strain.

Bermudes et al., WO99/13053 has told about some compositions and method, is used for the msbB gene that heredity destroys Salmonella, and consequent Salmonella is compared with wild type has lower TNF α inducibility and lower toxicity.In certain embodiments, some sudden change Salmonellas are compared with wild type salmonella, to the sensitivity raising of chelating agen.Also can be with reference to Low et al., 1999, Nature Biotech.17:37-47.

In the 2nd joint of the application's book or any chapters and sections, quote or all lists of references of indicating can not be interpreted as all admitting that these lists of references are prior arts of the present invention.

3. Summary of the invention

The invention provides certain methods, be used for one or more primary effector molecules are delivered to solid tumor.In an embodiment, these methods can be used to send high-caliber one or more primary effector molecules.In detail, the invention provides certain methods, be used for by being oriented to the attenuated bacteria of tumor, the Salmonella that host's toxicity is reduced for example, can toxigenicity when whole body is delivered medicine to the host or the primary effector molecule local delivery of inducing ill effect (as bad immunological role) to tumor.The present invention includes the preparation and the purposes that are oriented to the attenuated bacteria of tumor such as Salmonella etc., with its as carrier one or more primary effector molecules and optionally one or more second order effect molecules be delivered to suitable site of action, as the solid tumor position.In particular, the attenuated bacteria that is oriented to tumor of the present invention is through processing one or more primary effector molecules of codified and the optionally facultative aerobe or the facultative anaerobe of one or more second order effect molecules.

The invention provides the attenuated bacteria that is oriented to tumor, this antibacterial can be expressed the coding nucleic acid molecule of primary effector molecule at the solid tumor position through processing.In a special embodiment, this attenuated bacteria that is oriented to tumor can be expressed a kind of a kind of coding nucleic acid molecule of primary effector molecule through processing.In another embodiment, this attenuated bacteria that is oriented to tumor can be expressed one or more coding nucleic acid molecules of one or more primary effector molecules through processing.According to this embodiment, single bacterial isolates can be processed into one or more coding nucleic acid molecules that to express one or more primary effector molecules at the solid tumor position.In another embodiment, more than one the attenuated bacteria bacterial strain that is oriented to tumor can be processed into one or more coding nucleic acid molecules that can express one or more primary effector molecules.In this embodiment, a kind of mode is to adopt the attenuated bacteria bacterial strain that is oriented to tumor of the same race.Another kind of mode is to adopt the attenuated bacteria bacterial strain that is oriented to tumor (as Listerella and Salmonella) not of the same race.

Primary effector molecule of the present invention can be used for treating solid tumor, as cancer, melanoma, lymphoma or sarcoma." treatment of solid tumor " or " the treatment solid tumor " that use in the literary composition comprise, suppress tumor or tumor cell growth, dwindle tumor size, kill tumor cell, or prevent tumor cell diffusion (transfer).In a special embodiment, primary effector molecule of the present invention can be induced a kind of partial immunne response at tumor locus, this immunne response can suppress growth, the kill tumor cell of tumor or tumor cell, or prevents that tumor cell is diffused into other positions of health.Therefore, these primary effector molecules can provide the tumor treatment effect.

These primary effector molecules can derive from any known biology, comprising, but be not limited to animal, plant, antibacterial, fungus, and protista or virus.In an embodiment of the present invention, the preferred employing derives from a kind of mammiferous primary effector molecule.In this embodiment, more preferably adopt the primary effector molecule that derives from the people.Primary effector molecule of the present invention comprises TNF family member, anti-angiogenesis, cytotoxicity polypeptide or peptide, tumor suppression enzyme, and functional fragment.

In a special embodiment, primary effector molecule of the present invention is TNF family member or its functional fragment.TNF family member's example comprises, but be not limited to tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), TNF-α apoptosis induction ligand related (TRAIL), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis, CD40 part (CD40L), LT-α (lymphotoxin α), LT-β (lymphotoxin-beta), OX40L (OX40 part), FasL, CD27L (CD27 part), CD30L (CD30 part), 4-1BBL, APRIL (a kind of proliferation-inducing ligand), LIGHT (the II type transmembrane protein of a kind of 29kDa that produces by activated T cells), TL1 (a kind of tumor necrosis factor like cell factor), TNFSF16, TNFSF17 and AITR-L (activation-inducing type TNFR family member's part).In a preferred embodiment, primary effector molecule of the present invention is tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis and CD40 part (CD40L), or its functional fragment.

In another special embodiment, primary effector molecule of the present invention is anti-angiogenesis or its functional fragment.The example of anti-angiogenesis comprises, but be not limited to, interior chalone, angiostatin, apomigren, the angiogenesis inhibitor Antithrombin III, the 29kDa N-end protein hydrolysis fragment of fibronectin and 40kDa C-end protein hydrolysis fragment, the uPA receptor antagonist, the 16kDa proteolytic fragments of prolactin antagonist, the 7.8kDa proteolytic fragments of PF4, PF4 contain 24 amino acid whose angiogenesis inhibitor fragments, be called as 13.40 anti-angiogenesis, thrombospondin I's contains 22 amino acid whose angiogenesis inhibitor fragments of peptides, SPARC's contains 20 amino acid whose angiogenesis inhibitor fragments of peptides, the peptide that contains RGD and NGR, the angiogenesis inhibitor small-molecular peptides of laminin, the angiogenesis inhibitor small-molecular peptides of fibronectin, precollagenous angiogenesis inhibitor small-molecular peptides, the angiogenesis inhibitor small-molecular peptides of EGF, and beta 2 integrin alpha _vβ ₃Peptide antagonists and the peptide antagonists of vegf receptor.In a preferred embodiment, primary effector molecule of the present invention is interior chalone, apomigren's or thrombospondin I's functional fragment.

In another special embodiment, primary effector molecule of the present invention is cytotoxicity polypeptide or peptide, or its functional fragment.The example of cytotoxicity polypeptide or peptide comprises, but be not limited to strong competitive inhibitor CAAX tetrapeptide, cyclin inhibitor, Raf inhibitors of kinases, CDC inhibitors of kinases, caspases, p53, p16 and the p21 of bacteriocin family member, Vero cytotoxin, cytotoxicity necrosin 1 (CNF1), cytotoxicity necrosin 2 (CNF2), Pasteurella multocida toxin (PMT), pseudomonas endotoxin, hemolysin, farnesyl transferase.In a preferred embodiment, primary effector molecule of the present invention is the bacteriocin family member, and condition is that this bacteriocin family member is not that a kind of bacteriocin discharges albumen (BRP).Bacteriocin family member's example comprises, but be not limited to, ColE1, ColE1a, ColE1b, ColE2, ColE3, ColE4, ColE5, ColE6, ColE7, ColE8, ColE9, colicine A, colicine K, colicine L, colicine M, cloacin DF13, pesticin A1122, staphylococcin 1580, butyricin 7423, pyocin R1 or AP41, megacin A-216, and vibriobactins Vibriobactin..In a special embodiment, primary effector molecule of the present invention is colicine E3.

In another special embodiment, primary effector molecule of the present invention is tumor suppression enzyme or its functional fragment.The example of tumor suppression enzyme includes, but are not limited to, methioninase, asparaginase, lipase, phospholipase, protease, ribonuclease (not comprising colE3), DNA enzyme and glycosidase.In a preferred embodiment, primary effector molecule of the present invention is a methioninase.

The present invention also provides certain methods, the attenuated bacteria that is used for being oriented to tumor by Salmonella etc. with one or more primary effector molecules and one or more second order effect molecules with the compound mode local delivery to the solid tumor position.In a special embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of coding nucleic acid molecule of a kind of primary effector molecule and a kind of second order effect molecule through processing.In another embodiment, the attenuated bacteria that is oriented to tumor can be expressed one or more coding nucleic acid molecules of one or more primary effector molecules and one or more second order effect molecules through processing.According to this embodiment, single bacterial isolates can be processed into one or more coding nucleic acid molecules that to express one or more primary effector molecules and one or more second order effect molecules at the solid tumor position.In another embodiment, more than one the attenuated bacteria bacterial strain that is oriented to tumor can be processed into one or more coding nucleic acid molecules that to express one or more primary effector molecules and one or more second order effect molecules at the solid tumor position.In this embodiment, a kind of mode is to adopt the attenuated bacteria bacterial strain that is oriented to tumor of the same race.Another kind of mode is to adopt the attenuated bacteria bacterial strain that is oriented to tumor (as Listerella and Salmonella) not of the same race.

Second order effect molecule of the present invention provides extra antineoplaston activity, the attenuated bacteria that promotion is oriented to tumor to discharge primary effector molecule, and (perhaps) strengthens the internalization of site of actions such as solid tumor position.Second order effect molecule of the present invention can contain a kind of molecule (for example a kind of anti-tumor protein, comprising, but be not limited to cytotoxin, enzyme and bacteriocin; The prodrug invertase; Antisense molecule; Ribozyme; Antigen; Or the like), this molecule can be worked in coordination with by method of the present invention and primary effector molecule and be sent, with solid tumors such as treatment cancer, melanoma, lymphoma or sarcomas.

These second order effect molecules can derive from any known biology, comprising, but be not limited to animal, plant, antibacterial, fungus, and protista or virus.Adopt the second order effect molecule that derives from a kind of antibacterial or virus in certain embodiments of the invention.In some preferred embodiment of the present invention, adopt the second order effect molecule (as BRP) that derives from a kind of antibacterial.In some other preferred embodiment of the present invention, adopt the second order effect molecule (as TAT) that derives from a kind of virus.In other preferred embodiments of the present invention, adopt and derive from a kind of mammiferous second order effect molecule.In some preferred embodiment, adopt the second order effect molecule that derives from the people.

The invention provides the attenuated bacteria that is oriented to tumor that some contain effector molecule, but these effector molecules are by plasmid or transfection nucleic acid coding.In a preferred embodiment of the present invention, the attenuated bacteria that is oriented to tumor that uses is Salmonella.When the attenuated bacteria that is oriented to tumor when Salmonella etc. can be expressed more than one effector molecule (as elementary effector molecule or second order effect molecule); these effector molecules can be encoded by identical plasmid or nucleic acid, also can be encoded by more than one plasmid or nucleic acid.The present invention also provides some attenuated bacterias that are oriented to tumor that contain effector molecule, and these effector molecules are by a kind of nucleic acid coding that is incorporated in the bacterial genomes.The effector molecule of integrating can be the endogenous molecule that Salmonella etc. is oriented to the attenuated bacteria of tumor, also can be introduced in the attenuated bacteria that is oriented to tumor and (for example introduce a kind of nucleic acid of codified effector molecule, but as plasmid transfection nucleic acid, transposon, or the like), make this nucleic acid of coded actions molecule can be incorporated in the genome of the attenuated bacteria that is oriented to tumor.The invention provides a kind of and the suitable nucleic acid molecules of the coded actions molecule that is connected of promoter operability.The promoter that is connected with the nucleic acid operability of coded actions molecule can be homologous (promptly own), also can be allogenic (nucleic acid itself that is the coded actions molecule does not have).Suitably the example of promoter includes, but are not limited to Tet promoter, trc, pepT, lac, sulA, pol II (dinA), ruv, recA, uvrA, uvrB, uvrD, umuDC, lexA, cea, caa, recN and pagC.

The present invention also provides certain methods, is used for by the attenuated bacteria that is oriented to tumor the fusion rotein that one or more contain signal sequence and effector molecule being carried out local delivery.In a preferred embodiment, the attenuated bacteria that is oriented to tumor can be expressed one or more coding nucleic acid molecules of one or more fusion rotein through processing, these fusion rotein contain a kind of Omp sample albumen or its part (as signal sequence, targeting sequencing, pericentral siphon district, membrane spaning domain, multispan membrane structure territory, or its combination, the definition of the 3.1st joint to " Omp sample albumen " sees below), and contain a kind of effector molecule.Although be not subjected to the restriction of principle, the inventor thinks that Omp sample albumen can or be adhered to adventitia with the effector molecule grappling, or can be used to make effector molecule to be positioned bacterial outer membrane.In certain embodiments, effector molecule of the present invention can be strengthened sending to bacterial outer membrane.In an embodiment, effector molecule and the proteic fusion of Omp sample are used to the accelerating effect molecule and are positioned pericentral siphon.In some other embodiment, effector molecule and the proteic fusion of Omp sample are used to the release of accelerating effect molecule.The proteic example of Omp sample comprises, but be not limited to, below at least a portion of each example: OmpA, OmpB, OmpC, OmpD, OmpE, OmpF, OmpT, porin sample albumen, PhoA, PhoE, lamB, beta-lactamase, enterotoxin, protein A, endoglucanase, the relevant lipoprotein (PAL) of Peptidoglycan, FepA, FhuA, NmpA, NmpB, NmpC and a kind of main outer membrane lipoprotein (as LPP).In other embodiments of the present invention, fusion rotein of the present invention contains a kind of Proteolytic enzyme shearing site.This Proteolytic enzyme shearing site can be the endogenous site of effector molecule, also can be the proteic endogenous site of Omp sample, also can be the Proteolytic enzyme shearing site that is building up in the fusion rotein.

The present invention also provides certain methods, be used for by being oriented to tumor attenuated bacteria with one or more contain transport peptide and effector molecule the fusion rotein local delivery to solid tumor.Studies show that, in fusion rotein, use transport peptide can be beneficial to nearly all cell to the range of scatter that is in its generation or introducing of desired polypeptides or delivery of peptides (can reference, for example, Bayley, 1999, Nature Biotechnology 17:1066-1067; Fernandez et al., 1998, Nature Biotechnology 16:418-420; With Derossi et al., 1998, Trends Cell Biol.8:84-87).Therefore, the attenuated bacteria that is oriented to tumor is processed into expresses the method that contains the fusion rotein that transports peptide and effector molecule and can improve effector molecule by the ability of tumor cell internalization.In a special embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of nucleic acid molecules, a kind of fusion rotein that transports peptide and effector molecule that contains of this nucleic acid molecules codified through processing.In another embodiment, the attenuated bacteria that is oriented to tumor can be expressed one or more nucleic acid molecules through processing, and one or more contain the fusion rotein that transports peptide and effector molecule these nucleic acid molecules codifieds.Effector molecule in these embodiments can be a primary effector molecule, also can be the second order effect molecule.The example that transports peptide includes, but are not limited to, and derives from HIV TAT albumen, feeler foot homeodomain (penetrating albumen (penetratin)), Ka Boxi fibroblast growth factor (FGF) membrane translocation sequence (MTS), and the peptide of herpes simplex virus VP22.

The present invention also provides certain methods, is used for by the attenuated bacteria that is oriented to tumor one or more being contained signal peptide, transporting the fusion rotein local delivery of peptide and effector molecule to solid tumor.In a special embodiment, the attenuated bacteria that is oriented to tumor can be expressed one or more nucleic acid molecules through processing, and one or more contain these nucleic acid molecules codifieds signal peptide, transport the fusion rotein of peptide and effector molecule.Effector molecule in this embodiment can be a primary effector molecule, also can be the second order effect molecule.

The present invention also provides certain methods, is used for by the attenuated bacteria that is oriented to tumor one or more being contained signal peptide, Proteolytic enzyme shearing site, transporting the fusion rotein local delivery of peptide and effector molecule to solid tumor.In a special embodiment, the attenuated bacteria that is oriented to tumor can be expressed one or more nucleic acid molecules through processing, and one or more contain these nucleic acid molecules codifieds signal sequence, Proteolytic enzyme shearing site, transport the fusion rotein of peptide and effector molecule.Effector molecule in this embodiment can be a primary effector molecule, also can be the second order effect molecule.

In certain embodiments, single bacterial isolates can be processed into one or more coding nucleic acid molecules that to express fusion rotein of the present invention at the solid tumor position.In some other embodiment, more than one the attenuated bacteria bacterial strain that is oriented to tumor can be processed into one or more coding nucleic acid molecules that to express one or more fusion rotein of the present invention at the solid tumor position.The mode of these embodiments is to adopt the attenuated bacteria bacterial strain that is oriented to tumor of the same race.Another kind of mode is to adopt the attenuated bacteria bacterial strain that is oriented to tumor (as Listerella and Salmonella) not of the same race.

The present invention also provides certain methods, be used for attenuated bacteria by being oriented to tumor with one or more fusion rotein of the present invention and one or more effector molecule local deliveries of the present invention to the solid tumor position.Preferably, compare with single expression fusion rotein or single expression effector molecule, expressed fusion protein and effector molecule can improve inhibition level to tumor growth or growth of tumour cell to the attenuated bacteria that is oriented to tumor simultaneously at the solid tumor position.

The present invention also is provided at the method for expressing a kind of primary effector molecule and optional a kind of second order effect molecule in the attenuated bacteria that Salmonella etc. is oriented to tumor, and antibacterial wherein has a kind of enhancing delivery system.In a preferred embodiment of the present invention, strengthen to discharge that to express a kind of releasing factor relevant with the attenuated bacteria that is oriented to tumor.In an embodiment, this discharge to allow effector molecule from the Cytoplasm space or periplasmic space discharge.Releasing factor can be the castle's intrinsic factor that is oriented to the attenuated bacteria of tumor, also can be exogenous factor (just a kind of coding molecule that itself is not had by the attenuated bacteria that is oriented to tumor is encoded).Releasing factor can be encoded by nucleic acid such as plasmids, also can be encoded by the nucleic acid that is incorporated in the attenuated bacteria genome that is oriented to tumor.Releasing factor can be encoded by the same nucleic acid or the plasmid of coding primary effector molecule, also can be encoded by different nucleic acid or plasmid.Releasing factor can be encoded by the same nucleic acid or the plasmid of coding second order effect molecule, also can be encoded by different nucleic acid or plasmid.In a preferred embodiment, releasing factor is that bacteriocin discharges albumen (BRP).In a special embodiment, BRP is the BRP of cloacin DF13 plasmid, a kind of BRP of colicine E1-E9 plasmid, or a kind of BRP of colicine A, N or D plasmid.In a preferred embodiment, the BRP that uses is the BRP (pCloDF13 BRP) of cloacin DF13.In another embodiment of the present invention, this enhancing delivery system comprises a kind of overexpression of porin.

The present invention also is provided at the method for expressing a kind of fusion rotein of the present invention in the attenuated bacteria that Salmonella etc. is oriented to tumor, and antibacterial wherein has a kind of enhancing delivery system.In a special embodiment, the expression of releasing factor is to carry out in a kind of cell, and this cell can also be expressed a kind of primary effector molecule and proteic fusion rotein of Omp sample of containing.In this embodiment, the coexpression of releasing factor can promote this fusion rotein to discharge from periplasmic space.

In an embodiment, the invention provides certain methods, the bacterial strain through modifying that is used for the attenuated bacteria by being oriented to tumor is sent high-caliber effector molecule or fusion rotein, and these can optionally accumulate in the tumor in expression effect molecule or fusion rotein through bacterial strains of modifying.In a kind of specific method, the modification bacterial strain that is oriented to the attenuated bacteria of tumor optionally increases the interior effector molecule of tumor.Although following chapters and sections are to be that reference is told about with the Salmonella for the sake of simplicity, the compositions and methods of the invention never are confined to Salmonella, but also comprise other any suitable antibacterials.In particular, the invention provides a kind of attenuated bacteria that is oriented to tumor, this antibacterial can be a facultative aerobe, also can be facultative anaerobe.The example that is oriented to the attenuated bacteria of tumor includes, but are not limited to, escherichia coli, and comprising enteroinvasive E.Coli, Salmonella, shigella dysenteriae, Yersinia enterocolitica, listerisa monocytogenes in mjme, mycoplasma hominis, and streptococcus.

The present invention also provides some Pharmaceutical compositions, these compositionss contain a kind of pharmaceutically suitable carrier thing and a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these one or more primary effector molecules of nucleic acid molecules codified.The present invention also provides some Pharmaceutical compositions, these compositionss contain a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these one or more primary effector molecules of nucleic acid molecules codified and one or more second order effect molecules.The present invention also provides some Pharmaceutical compositions, these compositionss contain a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these nucleic acid molecules codifieds one or more fusion rotein of the present invention.In addition, the present invention also provides some Pharmaceutical compositions, these compositionss contain a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through modifying, these nucleic acid molecules codifieds one or more fusion rotein of the present invention and one or more effector molecules (be primary effector molecule or (with) second order effect molecule).In a preferred embodiment, the attenuated bacteria that is oriented to tumor is a Salmonella.

Pharmaceutical composition of the present invention can be used to treat solid tumor.Solid tumor comprises, but be not limited to, sarcoma, cancer, lymphoma and other solid tumor cancers, comprising, but be not limited to germ cell line tumor, central nervous system's tumor, breast carcinoma, carcinoma of prostate, cervical cancer, uterus carcinoma, pulmonary carcinoma, ovarian cancer, carcinoma of testis, thyroid carcinoma, astrocytoma, glioma, cancer of pancreas, gastric cancer, hepatocarcinoma, colon cancer, melanoma, renal carcinoma, bladder cancer and mesothelioma.

The present invention also provides some to send the method for primary effector molecule, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to a kind of animal that needs this treatment, preferably a kind of mammal, people most preferably, said composition contains a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these one or more primary effector molecules of nucleic acid molecules codified.The present invention also provides some to send the method for primary effector molecule, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to a kind of animal that needs this treatment, preferably a kind of mammal, people most preferably, said composition contains a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these one or more primary effector molecules of nucleic acid molecules codified and one or more second order effect molecules.The present invention also provides some to send the method for primary effector molecule, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to a kind of animal that needs this treatment, preferably a kind of mammal, people most preferably, said composition contains a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these nucleic acid molecules codifieds one or more fusion rotein of the present invention.In addition, the present invention also provides some to send the method for primary effector molecule, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to a kind of animal that needs this treatment, preferably a kind of mammal, people most preferably, said composition contains and a kind ofly comprises the attenuated bacteria that is oriented to tumor of one or more nucleic acid molecules through processing, these nucleic acid molecules codifieds one or more fusion rotein of the present invention and one or more effector molecules (be primary effector molecule or (with) second order effect molecule).In a preferred embodiment, the attenuated bacteria that is oriented to tumor is a Salmonella.In a kind of specific method, the attenuated bacteria that is oriented to tumor has a kind of enhancing delivery system.

In certain embodiments, the attenuated bacteria that is oriented to tumor of expressing one or more nucleic acid molecules through processing can use with other known cancer therapies are collaborative, these one or more effector molecules of nucleic acid molecules codified and (or) fusion rotein.For instance, the attenuated bacteria that is oriented to tumor of expressing one or more nucleic acid molecules through processing can use with chemotherapeutics is collaborative, these one or more effector molecules of nucleic acid molecules codified and (or) fusion rotein.The example of chemotherapeutics comprises, but be not limited to, cisplatin, ifosfamide, paclitaxel, taxanes, I type topoisomerase enzyme inhibitor is (as CPT-11, the holder pool is for bearing, 9-AC and GG-211), gemcitabine, vinorelbine, oxaliplatin, 5-fluorouracil (5-FU), folinic acid, vinorelbine, temodal, taxol, cytochalasin B, Gramicidin D, ipecine, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicine, amycin, daunorubicin, dihydroxy anthracin diketone, dithranol, mithramycin, actinomycin D, the 1-boldenone, melphalan, glucocorticoid, procaine, tetracaine, lignocaine, propranolol, and puromycin homologue and cyclophosphamide.As selection, the attenuated bacteria that is oriented to tumor of expressing one or more nucleic acid molecules through processing also can use with X-ray therapy is collaborative, these one or more effector molecules of nucleic acid molecules codified and (or) fusion rotein.

The present invention includes the attenuated bacteria that is oriented to tumor and the sequential administration or the concomitant dosing method of anticarcinogen, attenuated bacteria wherein through processing can express one or more effector molecules and (or) one or more coding nucleic acid molecules of fusion rotein.What the present invention includes the attenuated bacteria that is oriented to tumor and anticarcinogen has adjection or a synergistic combined method, attenuated bacteria wherein through processing can express one or more effector molecules and (or) one or more coding nucleic acid molecules of fusion rotein.

The present invention also comprises anticarcinogen and can express the combined method of the attenuated bacteria that is oriented to tumor of one or more nucleic acid molecules through processing, the effector molecule that these one or more site of actions of nucleic acid molecules codified are different and (or) fusion rotein.No matter this combined method has synergism and still has adjection, and a kind of improvement therapy of the dual function based on these therapeutic agents can be provided.Therefore, new combination treatment of the present invention is compared with the single preparation therapy that adopts one of two kinds of preparations, can produce higher curative effect.3.1. definition and abbreviation

" Salmonella " used in the literary composition comprises all Salmonella species, comprising salmonella typhi, Salmonella choleraesuls and Salmonella enteritidis.This paper also comprises the Salmonella of different serotypes, and for example, the mouse typhus serotype that is commonly referred to Salmonella typhimurium is the subgroup of Salmonella enteritidis.

Analog: the term that uses in the literary composition " analog " be meant with the function class of primary effector molecule or second order effect molecule like or an identical peptide species, this polypeptide might not contain and primary effector molecule or the similar or identical aminoacid sequence of second order effect molecule, also not necessarily has and primary effector molecule or the similar or identical structure of second order effect molecule.Polypeptide with similar aminoacid sequence is meant the polypeptide that one of meets the following conditions at least: (a) contain a kind of polypeptide of aminoacid sequence, the aminoacid sequence of primary effector molecule of describing in this sequence and the literary composition or second order effect molecule has at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 99% homogeneity; (b) by a kind of nucleotide sequence coded polypeptide, this sequence can be under stringent condition and the nucleotide sequence hybridization of primary effector molecule described in the coding literary composition or second order effect molecule, and hybridization sequences is at least 5 continuous amino acid residues, at least 10 continuous amino acid residues, at least 15 continuous amino acid residues, at least 20 continuous amino acid residues, at least 25 continuous amino acid residues, at least 40 continuous amino acid residues, at least 50 continuous amino acid residues, at least 60 continuous amino acid residues, at least 70 continuous amino acid residues, at least 80 continuous amino acid residues, at least 90 continuous amino acid residues, at least 100 continuous amino acid residues, at least 125 continuous amino acid residues, or at least 150 continuous amino acid residues; And (c) by a kind of nucleotide sequence coded polypeptide, this sequence has at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 99% homogeneity with the nucleotide sequence of primary effector molecule described in the coding literary composition or second order effect molecule.Polypeptide with similar structures of primary effector molecule described in the literary composition or second order effect molecule is meant the polypeptide of similar secondary structure, tertiary structure or quarternary structure with primary effector molecule described in the literary composition or second order effect molecule.The structure of polypeptide can be measured by method known to those skilled in the art, comprising, but be not limited to peptide sequencing method, X-radiocrystallography method, magnetic nuclear resonance method, circular dichroism method and crystal current microscopy survey method.

Anti-angiogenesis: anti-angiogenesis is meant any protein molecule with anti-angiogenesis activity, or the nucleic acid of encoding such proteins molecule.In a preferred embodiment, the anti-angiogenesis of use is a kind of bigger proteic fragments of peptides or shears fragment.

Attenuation: attenuation is meant a kind of method of modifying that makes the pathogenic reduction of microorganism or carrier.The final result of attenuation is, when attenuated microorganisms or carrier were delivered medicine to the patient, the danger of toxicity and other side effect reduced.

Bacteriocin: bacteriocin is meant the bacterial protein toxin with given activity, and bacterial host is to this toxin immunity.Bacteriocin can be by the genome of bacterial host or plasmid-encoded, its toxicity at the scopes of other antibacterials can be wide can be narrow, bacteriocin can be the simple structure that only contains one or two subunit, also can be many subunit structures.In addition, the host of expression bacteriocin has the immunity of this bacteriocin of opposing.

Chelating agen sensitivity: the definition of chelating agen sensitivity is, can influence the valid density of bacterial multiplication, maybe can reduce the concentration of bacteria living power, and bacteria living power is determined by reproducible colony forming unit (c.f.u.).

Derivant: the term " derivant " that uses in " derivant of a peptide species " of this paper is meant a peptide species, this peptide species contains a kind of reformed aminoacid sequence such as polypeptide such as primary effector molecule or second order effect molecules, the change method is to introduce amino acid residue to replace, lack or add, or polypeptide connects with the molecule generation covalency of arbitrary type.The term " derivant " that uses in " derivant of a kind of primary effector molecule or second order effect molecule " of this paper is meant adorned a kind of primary effector molecule or second order effect molecule, method of modifying is, for example, primary effector molecule or second order effect molecule connect with the molecule generation covalency of arbitrary type.As the example of indefiniteness, can be by primary effector molecule or second order effect molecule being modified such as Proteolytic enzyme shearing or the method that is connected with a kind of cell ligand or other albumen.Can modify (for example acidylate, phosphorylation, carboxylation, glycosylation, selenium are modified or sulphation) by technology well known by persons skilled in the art to the derivant of primary effector molecule or second order effect molecule with chemical modification method.In addition, the derivant of primary effector molecule or second order effect molecule can contain one or more nonclassical amino acids.Polypeptide derivative can have and primary effector molecule described in the literary composition or the similar or identical functions of second order effect molecule." be oriented to the attenuation salmonella mutant msbB of tumor at this paper ^-Derivant " in the term " derivant " that uses be meant the modification Salmonella msbB of definition in the 17th page of international open WO99/13053 ^-Mutant, this patent is this complete being incorporated herein by reference.

Fragment: the term that uses in the literary composition " fragment " is meant peptide or the polypeptide that contains a kind of aminoacid sequence, this sequence is at least 2 continuous amino acid residues of the aminoacid sequence of primary effector molecule or second order effect molecule, at least 5 continuous amino acid residues, at least 10 continuous amino acid residues, at least 15 continuous amino acid residues, at least 20 continuous amino acid residues, at least 25 continuous amino acid residues, at least 40 continuous amino acid residues, at least 50 continuous amino acid residues, at least 60 continuous amino acid residues, at least 70 continuous amino acid residues, at least 80 continuous amino acid residues, at least 90 continuous amino acid residues, at least 100 continuous amino acid residues, at least 125 continuous amino acid residues, at least 150 continuous amino acid residues, at least 175 continuous amino acid residues, at least 200 continuous amino acid residues, or at least 250 continuous amino acid residues.

Functional fragment: the term that uses in the literary composition " functional fragment " is meant a kind of fragment of primary effector molecule or second order effect molecule, this fragment can keep at least a function (as enzymatic activity, the anti-angiogenesis activity of effector molecule, or anti-tumor activity) of primary effector molecule or second order effect molecule.

Fusion rotein: the term that uses in the literary composition " fusion rotein " is meant a peptide species, this peptide species contains a kind of aminoacid sequence of primary effector molecule or second order effect molecule, or the aminoacid sequence of its functional fragment or derivant and a kind of heterologous polypeptide (as non-primary effector molecule or non-second order effect molecule).

Omp sample albumen: the Omp sample albumen in the literary composition comprises any bacterial outer membrane albumen or its part (as signal sequence, targeting sequencing, pericentral siphon district, membrane spaning domain, multispan membrane structure territory, or its combination).In a particularly embodiment, Omp sample albumen is OmpA, OmpB, OmpC, OmpD, OmpE, OmpF, OmpT, porin sample albumen, PhoA, PhoE, lamB, beta-lactamase, enterotoxin, protein A, endoglucanase, the relevant lipoprotein (PAL) of Peptidoglycan, FepA, FhuA, NmpA, NmpB, NmpC at least, or the part of a kind of main outer membrane lipoprotein (as LPP) etc.

Purification: the attenuated bacteria bacterial strain that " purification " in the literary composition is oriented to tumor does not contain contaminative albumen or aminoacid (as the fragment of killed bacterial) or culture medium substantially.Substantially do not contain contaminative albumen or the amino acid whose attenuated bacteria bacterial strain that is oriented to tumor comprises, contain have an appointment 30%, 20%, 10% or 5% (dry weight) following contaminative albumen or the amino acid whose attenuated bacteria preparation that is oriented to tumor.

Releasing factor: the releasing factor in the literary composition comprises any albumen or its functional part that can promote that cell component discharges.In an embodiment, the releasing factor of using discharges albumen as bacteriocin.Releasing factor includes, but are not limited to, and the plasmid-encoded bacteriocin of cloacin DF13 discharges albumen (BRP), the plasmid-encoded BRPs of colicine E1-E9, or colicine A, N or the plasmid-encoded BRPs of D.

Septic shock: septic shock is a kind of internal organs depletion that is caused, caused by compound cells factor cascade reaction by TNF-α.Microorganism or carrier induce the ability of TNF-α to can be used as a kind of criterion, are used for representing the relative ability that it induces septic shock.

Be oriented to tumor: the definition that is oriented to tumor is to compare the ability that can preferentially be positioned corresponding carcinous target cell or tissue and duplicate with corresponding non-cancerous cells or tissue.Therefore, the attenuated bacteria that Salmonella etc. are oriented to tumor can preferentially adhere to and (or) infect carcinous target cell, and (perhaps) can keep surviving in tumor environment.

Virulence: virulence is to describe a relational language of total pathogenecity, comprises the ability (specific definition that sees below) of killing Normocellular ability or inducing septic shock.

The bacterial strain name VNP20009 that uses in the literary composition (international open WO99/13053), YS1646 and 41.2.9 can exchange each other, and they all are meant 202165 the bacterial strain of being numbered of preservation in the American type culture collection.The bacterial strain name YS1456 that uses in the literary composition and 8.7 can exchange each other, and they all are meant 202164 the bacterial strain of being numbered of preservation in the American type culture collection.

Can more fully understand the present invention with reference to detailed Description Of The Invention hereinafter, the illustrative embodiment and the accompanying drawing of special embodiment.

4. The accompanying drawing summary

Fig. 1: sophisticated humanTNF-'s coded sequence.DNA sequence (SEQ ID NO:3) and protein sequence (SEQ ID NO:4) all provide.

Fig. 2: Salmonella VNP20009 serC ^-The preparation method of bacterial strain.

Fig. 3: in the Salmonella typhimurium, by the trc promoters driven TNF-α gene expression TNF-α that is incorporated in the chromosome.

Fig. 4: the coded sequence of the synthetic OmpA signal sequence (1-63 nucleotide) that merges with sophisticated humanTNF-(67-543 nucleotide).DNA sequence (SEQ ID NO:7) and protein sequence (SEQ ID NO:8) are all represented with the fusion constructs form.

Fig. 5: pericentral siphon location and the expression of OmpA/TNF-alpha fusion protein in escherichia coli (JM109 bacterial strain).

Fig. 6: the coded sequence of the OmpA signal sequence (1-63 nucleotide) that merges with sophisticated people TRAIL (67-801 nucleotide).DNA sequence of fusion constructs (SEQ ID NO:9) and protein sequence (SEQ ID NO:10) are all represented in the drawings.

Fig. 7: expression and the processing of OmpA/TRAI L fusion rotein in escherichia coli (JM109 bacterial strain).

Fig. 8: the fusion rotein coded sequence of the OmpA signal sequence (1-63 nucleotide) of human IL-2's (64-462 nucleotide) of ripe (C125A) and modification.DNA sequence of fusion constructs (SEQ ID NO:11) and protein sequence (SEQ ID NO:12) are all represented in the drawings.

Fig. 9: the sophisticated human IL-2's of merging with phoA (8L) or ompA (8L) composite signal peptide expression and processing.

Figure 10: the coded sequence of the modification phoA signal sequence (1-63 nucleotide) that merges with human IL-2's (64-462 nucleotide) of ripe (C125A).DNA sequence of fusion constructs (SEQ ID NO:13) and protein sequence (SEQ ID NO:14) are all represented in the drawings.

Figure 11: the anti-tumor in vivo effect of the humanTNF-'s of expression mature form Salmonella typhimurium attenuated strain.

The expression of Figure 12: BRP is to the influence of anti-tumor in vivo effect.This figure shows that suffering from the melanomatous C57BL/6 mice of B16 contrasts with (1) PBS; (2) VNP20009; (3) the average tumor size after the VNP20009 that has a pSW1 plasmid that contains the BRP gene handles over time.

Figure 13: anaerobic is carried out in the β-gal gene expression that is subjected to the pepT promoter regulation in the Salmonella induce.Figure 13 A explanation oxygen free condition is to the external evoked situation of β-gal expression of Salmonella YS1456 bacterial strain and VNP20009 bacterial strain.BRP, β-gal are expressed in Figure 13 B explanation, or induce the situation comparison in BRP and the β-gal body of VNP20009 Salmonella to the intracellular β-gal of tumor regulating liver-QI of all expressing.

Figure 14: tetracycline is carried out in the β-gal gene expression that is subjected to the Tet promoter regulation in the Salmonella induce.Dosage-response curve shows, concentration is about tetracycline below the 0.15 μ g/ml can produces a kind of linearity and reply, and higher concentration then makes to reply and weakens, and infers that its reason may be the antibiotic function of tetracycline.

Figure 15: six polyhistidyls of pTrc99a plasmid-Nei chalone (chalone in the HexaHIS-) are expressed.Figure 15 A shows that chalone is expressed in the HexaHIS-that is transformed into 3 kinds of independent clonings in the Salmonella (VNP20009).Figure 15 B shows that chalone is expressed in the HexaHIS-that is transformed into 5 kinds of independent clonings in the escherichia coli (DH5 α).Be numbered even swimming lane and show the not extract of inducing culture thing, be numbered the extract that shows the inductive corresponding culture of IPTG of inducing of odd number.

Figure 16: chalone is expressed in the HexaHIS-of YA3334 plasmid: carry out western blot analysis with anti-histidine antibody, make chalone in the HexaHIS-in the asd system (adopting the trc promoter) demonstrate correct size (～25kD) the band (the 1-8 road is equivalent to 8 and independently clones) of chalone in the HexaHIS-.

Figure 17: the VNP20009 cell of chalone is to the effect of C38 mouse colon cancer in expressing.This figure shows that the mice that suffers from the C38 tumor contrasts with (1) PBS; (2) have the asd-VNP20009 of sky YA3334 carrier; (3) asd-VNP20009 of expression six polyhistidyls-Nei chalone; (4) the average tumor size after the VNP20009 of expression six polyhistidyls-Nei chalone and BRP handles over time.

Figure 18: the VNP20009 cell of chalone is to the effect of DLD1 human colon carcinoma in expressing.This figure shows that the nude mice that suffers from the DLD1 tumor contrasts with (1) PBS; (2) have the asd of sky YA3334 carrier ^-VNP20009; (3) the average tumor size after the VNP20009 of expression six polyhistidyls-Nei chalone and BRP handles over time.

Figure 19: the lysate of the attenuation salmonella that is oriented to tumor of chalone is to the antiproliferative activity of endotheliocyte in the expressing human.This figure shows bFGF and is equivalent to 8 * 10 ⁸The lysate of individual antibacterial is to people's venous endothelial cell (HUVEC) inhibition of proliferation.Contrast is for containing the Salmonella that free pTrc plasmid is arranged.Each data point is the average of 4 measured values of 1 type testing acquisition.Sample is all proofreaied and correct according to bacterial population.

Figure 20: the lysate of the attenuation salmonella that is oriented to tumor of expression PF4 peptide (the 47-70 aminoacid of PF4) and thrombospondin peptide (13.40) is to the antiproliferative activity of endotheliocyte.This figure shows bFGF and is equivalent to 3.2 * 10 ⁸The lysate of individual antibacterial is to people's venous endothelial cell (HUVEC) inhibition of proliferation.Contrast is for containing the Salmonella that free pTrc plasmid is arranged.Each data point is the average of 4 measured values of 1 type testing acquisition.Sample is all proofreaied and correct according to bacterial population.

Figure 21: the structure of pE3.shuttle-1 carrier.

Figure 22: the structure of Col E3-CA38 carrier (GenBank numbers AF129270).The nucleotide sequence of ColE3-CA38 carrier is as described in the SEQ ID NO:1.Col E3-CA38 carrier contains 5 kinds of open reading frames, describes and SEQ ID NO:2-5 respectively.

Figure 23: the structure of Col E3-CA38/BRP-1 carrier.

Figure 24: block diagram shows the deadly unit quantity of the colicine E3 that each bacterial strain produces.

Figure 25: to the dizzy mensuration of the different strains that is exposed to ultraviolet light or x-ray.

Figure 26: 41.2.9/Col E3 is to the effect of C38 mouse colon cancer.

Figure 27: 41.2.9/Col/E3 is to the anti-tumor activity of the DLD1 human colon carcinoma in the NU/Nu mice.

Figure 28: 41.2.9/Col E3 is to the melanomatous effect of B16 Mus.

Figure 29: the cytotoxicity of the Salmonella of the escherichia coli CNF1 of expression cloning.

Figure 30: compare with normal Hela cell (B), the Hela cell (A) that is exposed to CNF1 shows and increases and the multinuclear phenomenon.

Figure 31: the msbB part (shown in figure 32) of the pCVD442-msbB carrier that shows with 3 '-5 ' direction, one section disappearance is arranged at the middle part of msbB, and contain inner NotI, PacI, SphI, SfiI, SwaI and DraI polylinker (SEQ ID NO:61) in its position.See Figure 32.

Figure 32: the restriction endonuclease map and the sketch map that are used for inserting then chromosomal pCVD442-msbB carrier at DmsbB regional cloning DNA.MsbBdel is 5 ' and the 3 ' zone of DmsbB; Mob RP4 is a transfer element, is used for plasmid is transferred to another kind of bacterial strain by a kind of bacterial strain.Bla is the beta-lactamase gene, can give the sensitivity to b-lactam antibioticses such as Carbenicillin and ampicillin.SacB is a gene of giving sucrose sensitivity.

Figure 33: 1) pCVD442-Tet-BRP-AB carrier, 2) homologous recombination that in Salmonella YS50102, carries out with the DmsbB chromosome copies, 3) chromosomal integration that in Salmonella YS50102, carries out, and the phage transduction that carries out subsequently is to VNP20009 strain, 4) obtain the 41.2.9-Tet-BRP-AB bacterial strain by the sucrose screening.OriR6K is the plasmid replication starting point; MobRP4 is transfer factor, is used for plasmid is transferred to another kind of bacterial strain by a kind of bacterial strain.Amp is the beta-lactamase gene, can give the sensitivity to b-lactam antibioticses such as Carbenicillin and ampicillin.SacB is a gene of giving sucrose sensitivity.Note: not drawn on scale.

Figure 34: be exposed to the SKOV3 cell after 72 hours, the cytotoxic percentage (average=8) that No. 26 of tetBRPAB clone and No. 31 clone and positive control are compared with negative control (HSC10 and 41.2.9).The cytotoxic expression of Vero is induced (seeing the clone the 26th and No. 31) by tetracycline.Handle (+) through tetracycline; Handle (-) without tetracycline.The positive control of cytotoxic percentage is an escherichia coli HSC10 bacterial strain.

Figure 35: there be not (1A) in the attenuation salmonella that is oriented to tumor and have the dizzy formation situation on blood agar under (1B) situation at tetracycline.Through processing and there be not (2A) in the attenuation salmonella that is oriented to tumor of constitutive expression SheA at tetracycline and have dizzy formation situation under (2B) situation.Express through processing and can not had (3A) at tetracycline by the attenuation salmonella that is oriented to tumor of the inductive SheA of tetracycline and have dizzy formation situation under (3B) situation.

Figure 36: (A) do not contain the sketch map of the TAT-apoptosis plain fusion protein of six polyhistidine tags.(B) contain the sketch map of the TAT-apoptosis plain fusion protein of six polyhistidine tags.(C) contain a kind of sketch map of TAT-apoptosis plain fusion protein of OmpA-8L signal sequence.

Figure 37: the coded sequence of TAT-apoptosis plain fusion protein.DNA sequence (SEQ ID NO:57) and protein sequence (SEQ ID NO:58) all provide.

Figure 38: the coded sequence of six polyhistidyls-TAT-apoptosis plain fusion protein.DNA sequence (SEQ ID NO:59) and protein sequence (SEQ ID NO:60) all provide.

Figure 39: VNP20009/ cyclophosphamide combination treatment is to the effect of the growth of the M27 pulmonary carcinoma in the C57BL/6 mice.

Figure 40: VNP20009/ mitomycin combination treatment is to the effect of the growth of the M27 pulmonary carcinoma in the C57BL/6 mice.

Figure 41: VNP20009/ cisplatin combination treatment is to the effect of the growth of the M27 pulmonary carcinoma in the C57BL/6 mice.

5. Detailed Description Of The Invention

The present invention uses the attenuated bacteria bacterial strain that is oriented to tumor to send high-caliber therapeutic primary effector molecule to tumor.Superiority of the present invention is to avoid the potential general toxicity (septic shock that causes as TNF-α) of some primary effector molecule.The invention provides to solid tumor and send one or more primary effector molecules and the optional method of one or more second order effect molecules.In more detail, the present invention includes the preparation and the purposes that are oriented to the attenuated bacteria of tumor such as Salmonella etc., with its as carrier one or more primary effector molecules and optionally one or more second order effect molecules be delivered to suitable site of action, as the solid tumor position.In particular, the attenuated bacteria that is oriented to tumor of the present invention is through processing one or more primary effector molecules of codified and the optionally facultative aerobe or the facultative anaerobe of one or more second order effect molecules.

Described delivery system based on the attenuated bacteria that is oriented to tumor can be delivered to one or more effector molecules the solid tumor position.The invention provides some safety and effective method, be used for by being oriented to the attenuated bacteria of tumor, the Salmonella that host's toxicity is reduced for example, can toxigenicity when whole body is delivered medicine to the host or the primary effector molecule local delivery that causes adverse side effect (as bad immunology influence) to tumor.The present invention also provides the attenuated bacteria that is oriented to tumor by a kind of, as Salmonella, sends one or more primary effector molecules and the optional combination delivering method of one or more second order effect molecules.The present invention also provides the combination delivering method of the different attenuated bacterias that are oriented to tumor, these antibacterials have one or more different primary effector molecules with (or) one or more different second order effect molecules.

The present invention also provides certain methods, be used for attenuated bacteria by being oriented to tumor with one or more fusion rotein local deliveries that contain effector molecule to the solid tumor position, these antibacterials can be expressed described fusion rotein through processing.In an embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of fusion rotein that contains signal peptide and effector molecule through processing.In another embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of fusion rotein that contains signal sequence, Proteolytic enzyme shearing site and effector molecule through processing.In another embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of fusion rotein that transports peptide and effector molecule that contains through processing.In another embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of fusion rotein that contains signal sequence, transports peptide and effector molecule through processing.In an other embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of fusion rotein that contains signal sequence, Proteolytic enzyme shearing site, transports peptide and effector molecule through processing.The attenuated bacteria that is oriented to tumor can be expressed one or more fusion rotein of the present invention and one or more effector molecules of the present invention through processing.

The present invention also provides some Pharmaceutical compositions, and these compositionss contain a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these one or more primary effector molecules of nucleic acid molecules codified.The present invention also provides some Pharmaceutical compositions, these compositionss contain a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these one or more primary effector molecules of nucleic acid molecules codified and one or more second order effect molecules.In addition, the present invention also provides some Pharmaceutical compositions, these compositionss contain a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor that comprises one or more nucleic acid molecules through processing, these one or more fusion rotein of nucleic acid molecules codified and one or more effector molecules.

The present invention also provides certain methods, be used for the intravital solid tumor of animal is treated, the step of these methods comprises, will be through processing the animal that the attenuated bacteria that is oriented to tumor that can express one or more nucleic acid molecules delivers medicine to needs this treatment, these one or more primary effector molecules of nucleic acid molecules codified.The present invention also provides certain methods, be used for the intravital solid tumor of animal is treated, the step of these methods comprises, will be through processing the animal that the attenuated bacteria that is oriented to tumor that can express one or more nucleic acid molecules delivers medicine to needs this treatment, these one or more primary effector molecules of nucleic acid molecules codified and one or more second order effect molecules.In addition, the present invention also provides certain methods, be used for the intravital solid tumor of animal is treated, the step of these methods comprises, the attenuated bacteria that is oriented to tumor that will comprise one or more nucleic acid molecules through processing delivers medicine to the animal of this treatment of needs, these one or more fusion rotein of nucleic acid molecules codified and one or more effector molecules.Preferably this animal is mammal (as Canis familiaris L., cat, horse, cattle, a monkey, or pig), and more preferably this animal is behaved.The example of solid tumor comprises, but be not limited to, sarcoma, cancer, lymphoma and other solid tumor cancers, comprising, but be not limited to breast carcinoma, carcinoma of prostate, cervical cancer, uterus carcinoma, pulmonary carcinoma, ovarian cancer, carcinoma of testis, thyroid carcinoma, astrocytoma, glioma, cancer of pancreas, gastric cancer, hepatocarcinoma, colon cancer, central nervous system's cancer, germ cell line cancer, melanoma, renal carcinoma, bladder cancer and mesothelioma.

Although be not subjected to the restriction of any principle, the inventor thinks that the present invention can make this effector molecule at the tumor locus orientation expression by sending the attenuated bacteria that is oriented to tumor that contains effector molecule.

In order to explain removing, the present invention describes in detail and is divided into following trifle: " bacteria carrier "; " primary effector molecule that is used for oncotherapy "; " with the second order effect molecule of primary effector molecule coexpression "; " derivant and analog "; " fusion rotein "; " expression vector "; " method and composition that is used to send ".5.1. Bacteria carrier

Any attenuated bacteria that is oriented to tumor can use in the method for the invention.In more detail, the attenuated bacteria that is oriented to tumor that uses in the method for the invention is facultative aerobe or facultative anaerobe.The example facultative aerobic or the amphimicrobian attenuated bacteria that is oriented to tumor that can use in the method for the invention comprises, but be not limited to, escherichia coli, comprising enteroinvasive E coli, Salmonella, shigella dysenteriae, Yersinia enterocolitica, listerisa monocytogenes in mjme, mycoplasma hominis, and streptococcus.

Here be described with some factors that are oriented to tumor character influencing attenuation character, these factors can be used to make up or screen the bacterial isolates that is suitable for using in the method for the invention.For example, the 6.1st joint of international open WO96/40238 has been described screening and the separation method of the antibacterial that is oriented to tumor, and the 6.2nd joint has been described the method for antibacterial attenuation, all is incorporated herein by reference at this.Some examples of the attenuated bacteria that is oriented to tumor have also been described, this all complete being incorporated herein by reference in the International Patent Application WO 99/13053.Be to adopt methods known in the art to modify antibacterial in certain embodiments of the invention, with its attenuation or highly attenuated.

The invention provides the attenuated bacteria that is oriented to tumor that some can be used as carrier, be used for sending separately of one or more primary effector molecules (as TNF family member, cytotoxic peptide or polypeptide, tumor suppression enzyme or anti-angiogenesis), or send with the collaborative of one or more second order effect molecules.The present invention also provides some to can be used as the attenuated bacteria that is oriented to tumor of carrier, is used for sending separately of one or more fusion rotein of the present invention, or sends with the collaborative of one or more effector molecules.In a preferred embodiment of the present invention, the attenuated bacteria that is oriented to tumor is a Salmonella, and this antibacterial can be expressed one or more nucleic acid molecules through processing, these nucleic acid molecules codified effector molecules and (or) fusion rotein.

Although following chapters and sections are told about with particular reference to Salmonella, the compositions and methods of the invention are in no way limited to Salmonella, but also comprise other any suitable antibacterials.Suitable bacterial species comprises, but be not limited to, escherichia coli, comprising enteroinvasive E coli, Salmonella, shigella dysenteriae, Yersinia enterocolitica, listerisa monocytogenes in mjme, mycoplasma hominis and streptococcus, wherein, these antibacterials are facultative aerobe or facultative anaerobe.5.1.1. The Salmonella carrier

The method of utilizing the present invention to tell about can make any attenuated bacteria that is oriented to tumor encode through processing one or more primary effector molecules and optional one or more second order effect molecules, thereby produces a kind of attenuated bacteria that is oriented to tumor that one or more effector molecules of the present invention is delivered to the novelty of solid tumor.In addition, the method of utilizing the present invention to tell about can make any attenuated bacteria that is oriented to tumor encode through processing one or more fusion rotein of the present invention and optional one or more effector molecules, thereby produces a kind of attenuated bacteria that is oriented to tumor that fusion rotein of the present invention and effector molecule can be delivered to the novelty of solid tumor.

Antibacterials such as Salmonella are the intravital a kind of pathogen of human or animal.Sepsis is exactly by salmonellal a kind of disease because the morbidity of septic shock can cause very high mortality rate, so this disease be one have important topic to be solved (Bone, 1993, ClinicalMicrobiol.Revs.6:57-68).Therefore, in order to use the Salmonella carrier in the present invention safely, need carry out attenuation to the pathogenic virulence of bacteria carriers such as Salmonella.In this application, attenuation comprises to be processed to reduce the pathogenic of this microbe carrier microbe carrier, this conforms to its traditional definition, to comprise in addition microbe carrier is processed, make the gained microbe carrier deliver medicine to the patient, still obtain to be similar to the effect that gives the pathogenic microorganism carrier with higher titre simultaneously with lower titre.Final result is to help reducing because of carrier being delivered medicine to the risk that the patient causes toxin shock or other side effect.This attenuated bacteria can adopt multiple technologies to separate.For instance, the method that realizes attenuation can be to remove or destroy those and guarantee antibacterial in host cell, especially the DNA sequences encoding of the virulence factor of surviving in macrophage and neutrophil cell.This removal or destroy technology are well-known in the art, comprising, for example, homologous recombination, chemomorphosis, radiation mutation, or transposon mutagenesis.With relevant those virulence factors of survival in macrophage usually can stress signal or host cell defense mechanism such as macrophage pinocytosis and express (Fields et al. at the macrophage internal specific with acidization etc., 1986, Proc.Natl.Acad.Sci.USA83:5189-5193).The table 4 of international open WO96/40238 has been enumerated the example of some Salmonella virulence factors, and the disappearance of these factors can cause attenuation.

The another kind of method of attenuating of bacteria carriers such as Salmonella is to modify causing this antibacterial to have toxic substituent group.For instance, the pathologic effect of bacterial sepsis mainly is to be caused by lipopolysaccharide (LPS) or endotoxin.The LPS component that causes this reaction is lipid A (" LA ").The toxic action of eliminating or alleviating LA can obtain the antibacterial of attenuation, because 1) patient's risk of producing septic shock reduces, and 2) can tolerate higher levels of bacteria carrier.

The change of the LA content of antibacterials such as Salmonella can realize by the method for introducing sudden change in the LPS biosynthesis pathway.In Salmonella, determine at present the several enzymatic steps of LPS biosynthesis pathway and the gene loci (Raetz, 1993, J.Bacteriol.175:5745-5753 and list of references thereof) of these steps of regulation and control, also found more corresponding sudden changes in addition.For example; one of them sudden change firA is a kind of sudden change in UDP-3-O (R-30 hydroxyl nutmeg acyl)-glycocyamine N-acyltransferase encoding gene; biosynthetic the 3rd step (the Kelley et al. of this kind of enzyme scalable endotoxin; 1993, J.Biol.Chem.268:19866-19874).The bacterial isolates that has this type of sudden change can produce a kind of lipid A different with the wild type lipid A, this lipid A contain one the 7th fatty acid and Palmic acid (Roy andColeman, 1994, J.Bacteriol.176:1639-1646).Roy and Coleman point out, firA ^-Sudden change not only can be blocked biosynthetic the 3rd step of endotoxin, but also can reduce lipid A 4 ' kinase whose activity, biosynthetic the 6th step of this kind of enzyme scalable lipid A.

Bacteria carrier of the present invention not only is attenuated, but also can be oriented to tumor, and that is to say, compare with normal structure, non-tumor or non-tumor cell, these antibacterials can preferentially adhere to, infected tumor or tumor cell, and (perhaps) can keep survival in tumor or tumor cell.The 6.1st joint (the 25-32 page or leaf of international open WO96/40238; Be oriented to tumor) and 6.2.2 joint (43-51 page or leaf; Attenuation) described the proper method that some acquisitions are oriented to the attenuated bacteria of tumor, all be incorporated herein by reference at this.Because the gained carrier has high degree of specificity and telegraphy metachromia, thereby along with the dilution increase of culture of microorganism, the gap of the bacterial infection quantity that occurs in bacterial infection quantity that occurs in target tumor or target tumor cell and the non-carcinous homologue is also increasing, to such an extent as to use the microbe carrier of lower titre also can obtain positive findings.The technology of telling about among the international open WO96/40238 also can be used to produce attenuation salmonella or the non-Salmonella carrier that is oriented to tumor.

The msbB that describes among the international open WO99/13053 ^-The mutant salmonella body is an illustrative example that has the attenuated bacteria that is oriented to tumor of LPS approach sudden change, and this patent is hereby incorporated by; Especially save relevant msbB with reference to 6.1.2 ^-The description of mutant salmonella bulk properties.MsbB ^-One of characteristic of Salmonella is that the ability of inducing TNF-α to reply is lower than the wild-type bacterium carrier.MsbB ^-The inductive TNF-alpha expression of Salmonella level is about the 5%-40% of wild type salmonella.

Utilize commercial mensuration system,, can reply the inductive TNF-α of the LPS of intact bacterial or isolating LPS or purification and carry out evaluating in external or the body as enzyme-linked immunoassay (ELISA) system.Relative activity is judged with the TNF-α output of every colony forming unit (" c.f.u. ") or based on the TNF-α output of μ g/kg.The TNF-α output of every colony forming unit is low more, shows that the level of inducing TNF-α to produce is low more.In a preferred embodiment, msbB ^-The Salmonella carrier contains one or more primary effector molecules of the present invention and optional one or more second order effect molecules through processing.

The present invention also comprises the attenuation salmonella msbB that is oriented to tumor ^-The application of the bacterium that derives of mutant.The method of utilizing the present invention to tell about can make the attenuation salmonella msbB that is oriented to tumor ^-The deriving bacterium of mutant is through processing and encode one or more primary effector molecules and optional one or more second order effect molecules, thereby produces a kind of attenuated bacteria that is oriented to tumor that one or more effector molecules of the present invention is delivered to the novelty of solid tumor.

The stability of attenuation phenotype is very important, and it makes this bacterial strain can not revert back to the stronger phenotype of a kind of virulence in the therapeutic process to the patient.The method that obtains this stability can be for example, to destroy virulence gene by the disappearance on the chromosome level or other non-response sudden changes, rather than pass through the epistatic dominance method.

The another kind of method of guaranteeing the attenuation phenotype is with more than one attenuation mode antibacterial to be processed, and for example a kind of sudden change in the lipid A generation approach is as msbB ^-Sudden change (WO99/13053), and one or more auxotrophic mutations of one or more nutrients or metabolite, as Bochner, 1980, uracil biosynthesis, purine biosynthesis and the biosynthetic auxotrophic mutation of arginine that J.Bacteriol.143:926-933 describes.In a preferred embodiment, codified or express the msbB that is oriented to tumor of at least a primary effector molecule ^-Salmonella has the auxotrophic mutation of purine simultaneously.In certain embodiments, the codified or the attenuated bacteria that is oriented to tumor of expressing at least a primary effector molecule also carry out attenuation by the sudden change of AroA, msbB, PurI or SerC.In other embodiments, the codified or the attenuated bacteria that is oriented to tumor of expressing at least a primary effector molecule also carry out attenuation by the disappearance of AroA, msbB, PurI or SerC.

Therefore, can express and send one or more primary effector molecules and optional one or more second order effect molecules with any attenuated bacteria that is oriented to tumor in the method for the invention to solid tumor.In preferred embodiments, the attenuated bacteria that is oriented to tumor is built into and can expresses one or more primary effector molecules and optional one or more second order effect molecules.In addition, can express and send one or more fusion rotein and optional one or more effector molecules with any attenuated bacteria that is oriented to tumor in the method for the invention to solid tumor.In preferred embodiments, the attenuated bacteria that is oriented to tumor is built into and can expresses one or more fusion rotein and optional one or more effector molecules.5.2. The primary effector molecule that is used for oncotherapy

The invention provides with Salmonella etc. and be oriented to the method that the attenuated bacteria of tumor is sent elementary (or optionally secondary) effector molecule.Effector molecule of the present invention be protein molecule (as albumen, comprising, but be not limited to, the albumen of peptide, polypeptide, albumen, post translational modification, or the like).The present invention also provides the coding nucleic acid molecule of primary effector molecule of the present invention.

Primary effector molecule can derive from any known biology, comprising, but be not limited to animal, plant, antibacterial, fungus, and protista and virus.In a preferred embodiment of the present invention, the primary effector molecule of use derives from a kind of mammal.In a preferred embodiment, the primary effector molecule of use derives from the people.Primary effector molecule of the present invention comprises TNF family member, anti-angiogenesis, cytotoxicity polypeptide or peptide, tumor suppression enzyme, and functional fragment.

In a special embodiment, primary effector molecule of the present invention is TNF family member or its functional fragment.TNF family member's example comprises, but be not limited to tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis, CD40 part (CD40L), LT-α, LT-β, OX40L, CD40L, FasL, CD27L, CD30L, 4-1BBL, APRIL, LIGHT, TL1, TNFSF16, TNFSF17 and AITR-L.In a preferred embodiment, primary effector molecule of the present invention is tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis and CD40 part (CD40L), or its functional fragment.Relevant summary can reference, for example, Kwon, B.et al., 1999, Curr.Opin.Immunol.11:340-345 is to TNF family member's description.In addition, following table 1 has been enumerated the representative member's of TNF family classics name and standard name.In a preferred embodiment of the present invention, primary effector molecule of the present invention is tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis and CD40 part (CD40L).

Table 1

The TNF family member
The TNF family member		Classical name	The standard name
??LT-α	????TNFSF1	Classical name	The standard name
??LT-α	????TNFSF1	??TNF-α	????TNFSF2
??LT-β	????TNFSF3	??TNF-α	????TNFSF2
??LT-β	????TNFSF3	??OX40L	????TNFSF4
??CD40L	????TNFSF5	??OX40L	????TNFSF4
??CD40L	????TNFSF5	??FasL	????TNFSF6
??CD27L	????TNFSF7	??FasL	????TNFSF6
??CD27L	????TNFSF7	??CD30L	????TNFSF8
??4-1BBL	????TNFSF9	??CD30L	????TNFSF8
??4-1BBL	????TNFSF9	??TRAIL	????TNFSF10
??TRANCE	????TNFSF11	??TRAIL	????TNFSF10
??TRANCE	????TNFSF11	??TWEAK	????TNFSF12
??APRIL	????TNFSF13	??TWEAK	????TNFSF12
??APRIL	????TNFSF13	??LIGHT	????TNFSF14
??TL1	????TNFSF15	??LIGHT	????TNFSF14
??TL1	????TNFSF15	??---	????TNFSF16
??---	????TNFSF17	??---	????TNFSF16
??---	????TNFSF17	??AITR-L	????TNFSF18

In another special embodiment, primary effector molecule of the present invention is anti-angiogenesis or its functional fragment.The example of anti-angiogenesis comprises, but be not limited to, interior chalone, angiostatin, apomigren, the angiogenesis inhibitor Antithrombin III, the 29kDa N-end protein hydrolysis fragment of fibronectin and 40kDa C-end protein hydrolysis fragment, the uPA receptor antagonist, the 16kDa proteolytic fragments of prolactin antagonist, the 7.8kDa proteolytic fragments of PF4, PF4 contain 24 amino acid whose angiogenesis inhibitor fragments, be called as 13.40 anti-angiogenesis, thrombospondin I's contains 22 amino acid whose angiogenesis inhibitor fragments of peptides, SPARC's contains 20 amino acid whose angiogenesis inhibitor fragments of peptides, the peptide that contains RGD and NGR, the angiogenesis inhibitor small-molecular peptides of laminin, the angiogenesis inhibitor small-molecular peptides of fibronectin, precollagenous angiogenesis inhibitor small-molecular peptides, the angiogenesis inhibitor small-molecular peptides of EGF, and integral protein α _vβ ₃Peptide antagonists and the peptide antagonists of vegf receptor.

In a preferred embodiment of the present invention, primary effector molecule of the present invention is interior chalone.Natural interior chalone contains C end～180 aminoacid (Genbank of the code cDNA of the collagen protein of two kinds of splicing forms is numbered AF18081 and AF18082) of collagen protein XVIII.

In another preferred embodiment of the present invention, primary effector molecule of the present invention is plasminogen fragment (Genbank of plasminogen coded sequence is numbered NM_000301 and A33096).The angiostatin peptide itself contains four kinds of kringle domains of plasminogen, and kringle 1 to kringle 4.Studies show that the

kringle

1,2 and 3 of reorganization has the angiogenesis inhibitor characteristic of native peptides, and kringle 4 do not have this activity (Cao et al., 1996, J.Biol.Chem.271:29461-29467).Therefore, angiostatin effector molecule of the present invention contains at least a, the preferred kringle domain that is selected from kringle 1, kringle 2 and kringle 3 more than at least a.In a special embodiment, primary effector molecule of the present invention is a kind of people's angiostatin molecule or its combination that is selected from 40kDa isotype, 42kDa isotype and 45kDa isotype.In another embodiment, the primary effector molecule that uses is kringle 5 domains of plasminogen, and it is a kind of than the more effective angiogenesis inhibitor of angiostatin (angiostatin contains kringle 1-4 domain).

In another preferred embodiment of the present invention, primary effector molecule of the present invention is an Antithrombin III.After this Antithrombin III is called antithrombase, contains a kind of heparin land and a kind of and interactional avtive spot ring of thrombin that connects in blood vessel wall.Antithrombase can make this albumen produce a kind of conformation change with combining of heparin, thereby active ring can be interacted with thrombin, causes thrombin that this ring district is carried out the Proteolytic enzyme shearing.This shear event can cause antithrombase to produce another kind of conformation change, this variation (i) can change the interaction position of thrombin and antithrombase, and (ii) make this complex separate (Carrell, 1999, Science 285:1861-1862 and list of references thereof) with heparin.People (1999, Science 285:1926-1928) such as O ' Reilly find that the antithrombase after the shearing has very strong anti-angiogenesis activity.Therefore, in an embodiment, anti-angiogenesis of the present invention is the angiogenesis inhibitor antithrombase.When utilizing method of the present invention that this albumen is delivered to solid tumor, can process bacteria carrier, make it express total length antithrombase and a kind of proteolytic enzyme that Genbank is numbered NM_000488, but the cleavage reaction of this proteolytic enzyme catalysis antithrombase is to produce angiogenesis inhibitor albumen.This proteolytic enzyme is optional from thrombin, pancreatic elastase and people's neutrophil cell elastoser.In a preferred embodiment, the proteolytic enzyme that uses is pancreatic elastase.The recombinant expression method of functional pancreatic elastase see Shirasu described (Shirasu et al., 1987, J.Biochem.102:1555-1563).

In another preferred embodiment of the present invention, primary effector molecule of the present invention be fibronectin 40kDa and (or) the 29kDa proteolytic fragments.Expressing these segmental carriers can be produced by conventional method with the total length nucleic acid coding sequence (Genbank numbers X02761) of fibronectin precursor protein with about the narration of encoding proteins maturation method.In a preferred embodiment, the 40kDa of fibronectin and (or) the 29kDa fragment is to be expressed by the trc promoter regulation with the form of cytoplasmic protein, for example can be inserted in the pTrc99A plasmid.

In another preferred embodiment of the present invention, primary effector molecule of the present invention is a kind of antagonist of urokinase plasminogen activator (uPA) receptor.In one embodiment, the antagonist that uses is the dominant negative mutant of uPA (reference, for example, Crowley et al., 1993, Proc.Natl.Acad.Sci.USA 90:5021-5025).Another-kind of embodiment in, the antagonist that uses is peptide antagonists or its fusion rotein (Goodson et al., 1994, Proc.Natl.Acad.Sci.USA 91:7129-7133).In another embodiment, the antagonist of use is soluble dominant uPA receptor (Min et al., 1996, Cancer Res.56:2428-2433).

In another preferred embodiment of the present invention, primary effector molecule of the present invention is the 16kDa N-end fragment of prolactin antagonist, and this fragment contains 120 aminoacid approximately, or its bioactive fragment (Genbank of prolactin antagonist coded sequence number is NM_000948).In a special embodiment, this prolactin antagonist fragment contains a kind of Cys58-Ser58 sudden change, thereby avoids this albumen to form unnecessary disulfide bond crosslinking.

In another preferred embodiment of the present invention, primary effector molecule of the present invention is the PF4 fragment of 7.8kDa, in a special embodiment, the PF4 fragment of this 7.8kDa is the formal representation with fusion rotein, and the aminoterminal of this fusion rotein contains preceding 35 aminoacid of escherichia coli β-glucuronidase.In another embodiment, the heparin associativity lysine of PF4 is mutated into glutamic acid, and the gained variant protein has very strong anti-angiogenesis activity (Maione et al., 1991, Cancer Res.51:2077-2083).The Genbank of PF4 coded sequence is numbered NM_002619.

In another preferred embodiment of the present invention, primary effector molecule of the present invention is 13 the amino acid whose angiogenesis inhibitor small-molecular peptides fragments that contain of PF4, be called as 13.40 anti-angiogenesis, thrombospondin I's contains 22 amino acid whose angiogenesis inhibitor fragments of peptides, SPARC's contains 20 amino acid whose angiogenesis inhibitor fragments of peptides, the angiogenesis inhibitor small-molecular peptides of laminin, the angiogenesis inhibitor small-molecular peptides of fibronectin, precollagenous angiogenesis inhibitor small-molecular peptides, the angiogenesis inhibitor small-molecular peptides of EGF, or beta 2 integrin alpha _vβ ₃The small-molecular peptides antagonist or the small-molecular peptides antagonist of vegf receptor.In a special embodiment, these small-molecular peptides are expressed in placed in-line mode, to improve proteic stability.Remove the vegf receptor antagonist (Soker et al., 1993, J.Biol.Chem.272:31582-31588) outside, remaining small-molecular peptides sequence by Cao (1998, Prog.Mol.Subcell.Biol.20:161-176) provide.In a highly preferred embodiment, the small-molecular peptides of use contains RGD or NGR motif.In certain embodiments, the peptide that contains RGD or NGR is to provide on the surface of host bacteria, and method is for example, the code nucleic acid of this peptide in the frame and the code nucleic acid of one or more OmpA extracellular loop to be merged.

In another special embodiment, primary effector molecule of the present invention is cytotoxicity polypeptide or peptide, or its functional fragment.Cytotoxicity polypeptide or peptide pair cell have toxic action or inhibitory action, and method is, and be for example, synthetic or upset the growth that cell cycle suppresses cell by disturbing albumen.The mechanism of action of this type of product can be to shear rRNA or ribonucleoprotein, inhibition elongation factor, shear mRNA, thereby maybe can reduce synthetic other mechanism that cell can't be survived of albumen.

The example of cytotoxicity polypeptide or peptide includes, but are not limited to, bacteriocin family member, Vero cytotoxin, cytotoxicity necrosin 1 (CNF1; As escherichia coli CNF1 and Fei Shi vibrio CNF1), cytotoxicity necrosin 2 (CNF2), Pasteurella multocida toxin (PMT), hemolysin, the strong competitive inhibitor CAAX tetrapeptide of farnesyl transferase, saporin, the castor toxalbumin, Agglutinin, other ribosome inactivating proteins (RIPs), the pseudomonas extracellular toxin, the DNA synthetic inhibitor, rna synthesis inhibitor, protein synthesis inhibitor, antisensenucleic acids, other metabolic poisons are (as DNA or RNA shearing molecules such as DNA enzyme and ribonuclease, protease, lipase, phospholipase), prodrug invertase (as HSV thymidine kinase and antibacterial cytosine deaminase), the photoactivation porphyrin, the castor toxalbumin, castor toxalbumin A chain, corn RIP, gelonin, cell lethality expansion toxin, diphtheria toxin, diphtherotoxin, diphtheria toxin, diphtherotoxin A chain, trichosanthin, tritin, pokeweed antiviral protein (PAP), Mirabilis antiviral protein (MAP), Dianthins 32 and 30, Agglutinin, monodrin, bryodin, shiga toxin, a kind of protein biology synthesis catalytic inhibitor (reference in the Semen Cucumidis sativi, for example, International Application No. WO 93/24620), the pseudomonas extracellular toxin, the escherichia coli heat-labile toxin, the escherichia coli heat-stable toxin, EaggEC ST-1 (EAST), cytotoxic bioactive fragment, and other cytotoxicity polypeptide or peptides of those skilled in the art's understanding.The summary of relevant escherichia coli and Salmonella toxin can reference, for example, O ' Brian andHolmes, Protein Toxins of Escherichia coli and Salmonella inEscherichia and Salmonella.Cellular and Molecular Biology, Neidhardt et al. (eds.), pp.2788.2802, ASM Press, Washington, D.C.

In a preferred embodiment, the primary effector molecule that uses as the bacteriocin family member (reference, for example, Konisky, 1982, Ann.Rev.Microbiol.36:125-144), condition is that this bacteriocin family member is not that a kind of bacteriocin discharges albumen (BRP).Bacteriocin family member's example comprises, but be not limited to, ColE1, ColE1a, ColE1b, ColE2, ColE3, ColE4, ColE5, ColE6, ColE7, ColE8, ColE9, colicine A, colicine K, colicine L, colicine M, cloacin DF13, pesticin A1122, staphylococcin 1580, butyricin 7423, pyocin R1 or AP41, megacin A-216, plain and vibriobactins Vibriobactin. (the Jayawardene andFarkas-Himsley of microorganism, 1970, J.Bacteriology Vol.102 pp 382-388).Although colicine A, E1, E2, Ia, Ib, K, L and M also can be used as suitable primary effector molecule, but most preferred primary effector molecule be colicine E3 or V (reference, for example, Konisky, 1982, Ann.Rev.Microbiol.36:125-144).In this embodiment, another kind of preferred bacteriocin is a cloacin, most preferably cloacin DF13.

In a preferred embodiment, the primary effector molecule that uses is ColE1, ColE2, ColE3, ColE4, ColE5, ColE6, ColE7, ColE8, ColE9.Studies show that, colicine E3 (ColE3) has degree of depth cytotoxic effect (Smarda et al. to mammalian cell, 1978, Folia Microbiol.23:272-277), comprising degree of depth cytotoxic effect (Fiska et al. to a kind of leukaemia's model system, 1978, Experimentia 35:406-40).The ColE3 cytotoxicity be a kind of by suppress the 80S ribosome stop the synthetic function of albumen (Turnowsky et al., 1973, Biochem.Biophys.Res.Comm.52:327-334).In more detail, ColE3 has ribonuclease activity (Saunders, 1978, Nature 274:113-114).The ColE3 of native form is the albumen composition of a kind of 60kDa, contains ratio and be 1: 1 a kind of 50kDa albumen and a kind of 10kDa albumen, and bigger subunit has nuclease, and less subunit has the function that suppresses the 50kDa subunit.So the albumen of 50kDa can be used as a kind of cytotoxic protein (or toxin), and the albumen of 10kDa can be used as a kind of antitoxin.Therefore, in an embodiment, when utilizing ColE3 to divide the period of the day from 11 p.m. to 1 a.m as second order effect, can single expression or to be higher than ColE3 subunit or its active fragment bigger than the horizontal expression of small subunit.Another embodiment of the present invention is to be oriented to 50kDa toxin and the 10kDa antitoxin of coding ColE3 in the attenuated bacteria of tumor with single plasmid in Salmonella etc.In this embodiment, toxin/antitoxin can be used as a kind of screening system of the Salmonella that has plasmid, and this system can kill the Salmonella of plasmid disappearance by toxin.In another embodiment, the 10kDa antitoxin is positioned on the chromosome, and the colE3 toxin is positioned on the plasmid, and the two is separated from one another, thereby can hinder to other spread of germs (the 5.6th joint sees above).

In another preferred embodiment, the primary effector molecule that uses is cloacin DF13.Model of action and the ColE3 of cloacin DF13 are similar.The molecular weight of this albumen composition is 67kDa.The size of its one-component is 57kDa and 9kDa.DF13 has ribonuclease activity, can cause the potassium ion seepage of cell in addition.

In another preferred embodiment, the primary effector molecule that uses is colicine V (Pugsley, A.P.and Oudega, B. " Methods for Studying Colicinsand Their Plasmids " in Plasmids, a Practical Approach 1987, ed.By K.G.Hardy; Gilson, L.et al.EMBO are J.9:3875-3884).

In another embodiment, the primary effector molecule that uses is colicine E2 (with a kind of pair of subunit colicine of ColE3 similar, but have the endonuclease enzymatic activity, rather than ribonuclease activity); Can form the iontophoretic injection passage, thereby destroy the cell proton motive force and cause colicine A, El, Ia, Ib or the K of cell death; But the synthetic colicine L of Profilin, DNA and RNA; Can change the infiltration environment of cell and cause the colicine M of cell septicopyemia; Pesticin A1122 like model of action and the colicine category-B; Staphylococcin 1580, a kind of pore-forming bacteriocin; Can suppress RNA, DNA and the synthetic butyricin 7423 of albumen indirectly by the target actor of the unknown; Can come the pyocin P1 of cell killing or be similar to the proteic albumen of phage tail by the uncoupling of Repiration and solute transportation; Model of action is similar to the pyocin AP41 of colicine E2; Maybe can cause a kind of phospholipase of intracellular matter seepage, and megacin A-216 (summary of relevant bacteriocin can be with reference to Konisky, and 1982, Ann.Rev.Microbiol.36:125-144); Colicine A (Pugsley, A.P.and Oudega, B. " Methods for Studying Colicins and TheirPlasmids " in Plasmids, a Practical Approach 1987, ed.By K.G.Hardy).

Therefore, primary effector molecule can comprise any bacteriocin that describe in the literary composition or known in the art, and condition is that this bacteriocin is not that a kind of bacteriocin discharges albumen.

In another special embodiment, primary effector molecule of the present invention is tumor suppression enzyme or its functional fragment.The example of tumor suppression enzyme includes, but are not limited to, methioninase, asparaginase, lipase, phospholipase, protease, ribonuclease, DNA enzyme and glycosidase.In a preferred embodiment, the primary effector molecule that uses is methioninase.

Primary effector molecule of the present invention can be used for, and for example, treatment or prevention solid tumor are as cancer, melanoma, lymphoma or sarcoma.

The invention provides the nucleic acid molecules of a kind of primary effector molecule of codified.The present invention also provides one or more primary effector molecules of codified and the optional nucleic acid molecules of one or more second order effect molecules.The nucleic acid that the invention provides codified effector molecule of the present invention and be connected with a kind of suitable promoter operability.The nucleic acid of these coded actions molecules can be transcribed with optional participation, translates, located, the element of stability or the like carries out operability and is connected.

A kind of length of nucleic acid molecules of primary effector molecule of encoding is about 6-100,000 base pair.Preferably the length of this nucleic acid is about 20-50,000 base pair.More preferably the length of this nucleic acid molecules is about 20-10,000 base pair.More preferably the length of this nucleic acid molecules is about 20-4000 base pair again.5.3. Second order effect molecule with the primary effector molecule coexpression

In certain embodiments of the invention, primary effector molecule (as TNF family member, cytotoxic peptide or polypeptide, anti-angiogenesis, or the tumor suppression enzyme) can in bacteria carrier, be second order effect molecule coexpression optionally with another kind of molecule.The second order effect molecule can provide extra treatment function and (or) bacteria carrier that promotes to modify (can express at least a primary effector molecule and optionally one or more second order effect molecules) is released into surrounding with content.The term that uses in the literary composition " extra treatment function " is meant that the second order effect molecule can provide a kind of additional or synergism, cyto-inhibition to tumor, or cytotoxic effect, as the effect outside the elementary effector molecule effect.Thereby the second order effect molecule can be used as a kind of extra treatment factor and (or) releasing factor plays a role.Preferably, no matter the conduct treatment factor still is releasing factor (or the both is), and the second order effect molecule can be at predetermined position, and promptly tumor locus preferentially or is specifically activated or expresses.In certain embodiments, the second order effect molecule of use can have two kinds of functions, promptly promotes the release (as by promoting antibacterial cracking or accurate cracking) of antibacterial content and treatment function (as by the cytotoxicity to tumor cell) is provided.In some non-limiting embodiments, the cytotoxicity of second order effect molecule can be mediated by patient's immune system; And this second order effect molecule can have the effect of immunomodulator.

In certain embodiments of the invention, the attenuated bacteria that is oriented to tumor of the present invention can be expressed at least a second order effect molecule with anti-tumor activity through processing, that is to say that the expression of this second order effect molecule can cause the death of tumor or tumor cell, maybe can suppress its growth.

Second order effect molecule of the present invention can be protein molecular or nucleic acid molecules.Nucleic acid molecules can be two strands or single stranded DNA or two strands or single stranded RNA, also can be the three chain nucleic acid molecule.These nucleic acid molecules can have the effect of ribozyme or antisensenucleic acids etc.

Antisensenucleic acids is can be with bonded oligonucleotide of nucleic acid such as sequence-specific mode and mRNA or DNA.When antisensenucleic acids combines with the mRNA that contains complementary series, can hinder this mRNA translation (reference, for example, United States Patent (USP) 5,168,053; 5,190,931; 5,135,917 and 5,087,617).The three chain nucleic acid molecule is meant and can be combined into a kind of conllinear three chain molecules with double-stranded DNA and hinders the single stranded DNA transcribe (reference, for example, United States Patent (USP) 5,176,996) thus.

Ribozyme is a kind of RNA molecule, and it can shear the RNA substrate by specificity, as mRNA, thus the growth or the expression of inhibition or interference cell.Have at least shearing that the ribozyme of 5 kinds of known types can participate in the RNA chain with (or) be connected.Ribozyme can act on any rna transcription body, and can catalysis shear these transcriptions (reference, for example, United States Patent (USP) 5,272,262; United States Patent (USP) 5,144,019; With United States Patent (USP) 5,168,053,5,180,818,5,116,742 and 5,093,246).

Identical with the narration of relevant primary effector molecule above, coding second order effect molecule provided by the invention or the equal operability of nucleic acid that contains the second order effect molecule have connected a kind of selected promoter, and can optionally transcribe, translate, locate with other participations, the element of stability or the like carries out operability and is connected.In addition, the expression of second order effect molecule can be adopted promoter identical with primary effector molecule and internal ribosome binding site, also can adopt the promoter different with primary effector molecule.

The length of the nucleic acid molecules of coding second order effect molecule is about 6-100,000 base pair.Preferably the length of this nucleic acid molecules is about 20-50,000 base pair.More preferably the length of this nucleic acid molecules is about 20-10,000 base pair.More preferably the length of this nucleic acid molecules is about 20-4 again, 000 base pair.

The effector molecule nucleotide sequence of codified second order effect molecule (is seen GenBank) as everyone knows.The coding nucleic acid molecule of second order effect molecule can separate by standard method, as the probe hybridization in amplification (as PCR), genomic library or cDNA storehouse, the antibody screening of expression library, or chemosynthesis, or by merchandise resources or other source acquisitions, second order effect molecule wherein is a kind of cytotoxic factor or cytostatic factor, or its bioactive fragment, variant or derivant.

Be used for by nucleic acid molecules and oligonucleotide that method described in the literary composition is used can come by any method known to those skilled in the art synthesize (reference, for example, the world discloses WO93/01286, United States Patent (USP) 5,218,088; 5,175,269; With 5,109,124).Can be used as the oligonucleotide of antisense agents use and the authentication method of ribozyme is well-known in the art.5.3.1. The factor with additional procedures function

In certain embodiments of the invention, the attenuation bacteria carrier that is oriented to tumor of the present invention can be expressed at least a primary effector molecule, preferably this bacteria carrier is the Salmonella carrier, this bacteria carrier can also be expressed at least a second order effect molecule with anti-tumor activity, that is to say, the expression of this second order effect molecule can cause the death of tumor or tumor cell, maybe can suppress the growth of tumor or tumor cell or the diffusion of tumor cell, thereby improve the cytotoxic effect or the cyto-inhibition of primary effector molecule.In an embodiment, the second order effect molecule can be used as the replenishing of effect of primary effector molecule to the effect of tumor.In a preferred embodiment, the effect of second order effect molecule has super additional or concertedness, that is to say, be higher than the effect summation of individually dosed primary effector molecule and second order effect molecule.

In certain embodiments, the second order effect molecule pair cell of use has toxic action or inhibitory action, and method is by disturbing albumen to synthesize or upsetting the growth that cell cycle suppresses cell.The mechanism of action of this type of product can be for example, to shear rRNA or ribonucleoprotein, inhibition elongation factor, shear mRNA, thereby maybe can reduce synthetic other mechanism that cell can't be survived of albumen.The example of this second order effect molecule includes, but are not limited to, saporin, castor toxalbumin, Agglutinin and other ribosome inactivating proteins (RIPs).

In another embodiment, the second order effect molecule of use is a kind of prodrug invertase or its code nucleic acid, thereby the chemical property that promptly can regulate medicine produces a kind of enzyme of cytotoxic agent.In the 33rd page of people's such as Pawelek WO96/40238 and table 2, enumerated the illustrative example of some prodrug invertase, be hereby incorporated by.WO96/40238 has also told about certain methods, is used to produce the secreting type fusion rotein that contains this prodrug invertase.According to the present invention, if the prodrug invertase is with BRP releasing factor coexpressions such as (5.3.2 that sees above joints) then can not be secretory protein.In a special embodiment, the prodrug invertase that uses is cytochrome p450 NADPH oxidoreductase (the Murray et al. that can act on ametycin and methylmitomycin, 1994, J.Pharmacol.Exp.Therapeut.270:645-649).In another embodiment, releasing factor coexpressions such as second order effect molecule and BRP, and can cause the release of cofactor (as NADH, NADPH, ATP etc.), these cofactors can improve the activity of prodrug invertase.In this embodiment, another kind of mode is releasing factor coexpressions such as second order effect molecule and BRP, and can cause activating the release of medicine (for example activating in antibacterial kytoplasm or pericentral siphon, then a kind of medicine that is discharged by bacteria carrier).

In another embodiment, the second order effect molecule of use is a kind of inhibitor of inducible nitric oxide synthase (NOS) or endothelial nitric oxide synthase.Nitric oxide (NO) has been considered to participate in the adjusting and the arteriosclerosis of angiogenic growth.NO is acted on the L-arginine and is formed by nitricoxide synthase (NOS), and it can regulate immunne response, inflammatory reaction and cardiovascular response.

In another embodiment, the second order effect molecule that uses can be by suppressing to participate in the proteic generation or the active toxic action or the inhibitory action that forms pair cell of cell proliferation, as oncogene or somatomedin (as bFGF, int-2, hst-1/K-FGF, FGF-5, hst-2/FGF-6, FGF-8) or cell receptor or part.This inhibition can transcribe or translation skill on carry out (numerator mediated by a kind of second order effect, this second order effect molecule is a kind of ribozyme or triple strand dna), also can on the protein active level, carry out (numerator mediated by a kind of second order effect, this second order effect molecule is a kind of inhibitor of somatomedin approach, as a kind of dominant negative mutant).

In another embodiment, the second order effect molecule that uses is a kind of cytokine, chemotactic factor or immune modulator, or its code nucleic acid, as il-1 (IL-1), interleukin-2 (IL-2), interleukin-4 (IL-4), interleukin-5 (IL-5), IL-10 INTERLEUKIN-10 (IL-10), interleukin-15 (IL-15), il-1 8 (IL-18), endothelial mononuclear cell activator protein-2 (EMAP2), GM-CSF, IFN-γ, IFN-α, MIP-3 α, SLC, MIP-3 β or a kind of mhc gene, as HLA-B7.Sending this immunomodulatory effect molecule can regulate immune system, thereby improves the potential antineoplastic immune power of host.As selection, also can send the part B7.1 of costimulatory molecules such as CD28 and CTLA-4 and the coding nucleic acid molecule of B7.2 and strengthen the cell-mediated immunity of T.Another kind of immunomodulator is α-1, and 3-galactosyltransferase, this kind of enzyme are expressed the cytosis of killing that can produce complement-mediated on tumor cell.In addition, another kind of immunomodulator is a tumor associated antigen, promptly express by tumor cell specific, but not a kind of molecule that carcinous corresponding cell is not expressed, or the expression in tumor cell is higher than a kind of molecule of non-carcinous corresponding cell.The illustrative example of tumor associated antigen is at Kuby, Immunology, and W.H.Freeman and Company, New York, NY, 1stEdition (1992) describes among the pp.515-520 to some extent, and the document is hereby incorporated by.Other examples of tumor associated antigen are understood by those skilled in the art.

In another embodiment, the second order effect molecule that uses is Flt-3 part or its code nucleic acid.In another embodiment, the second order effect molecule that uses is BRP.

In a special embodiment, when elementary effector molecule was the TNF family member, then the second order effect molecule did not use the TNF family member.In another special embodiment, when elementary effector molecule was a kind of anti-angiogenesis, then the second order effect molecule did not use anti-angiogenesis.In another special embodiment, when the second order effect molecule was a kind of cytotoxic peptide or polypeptide, then the second order effect molecule did not use cytotoxic peptide or polypeptide.In another special embodiment, when elementary effector molecule was a kind of tumor suppression enzyme, then the second order effect molecule did not use the tumor suppression enzyme.5.3.2. Can promote the Graft Versus Tumor molecule to be discharged into the factor in the tumor environment

In some other embodiment of the present invention, the attenuation bacteria carrier that is oriented to tumor of the present invention can be expressed at least a primary effector molecule, preferably this bacteria carrier is the Salmonella carrier, this bacteria carrier can also be expressed at least a second order effect molecule, this second order effect molecule can make the cell membrane of antibacterial have permeability, can promote that maybe cellular content is discharged in the extracellular environment, as tumor locus, thus strengthen primary effector molecule and (or) the sending of second order effect molecule.Can make antibacterial have permeability maybe can promote this second order effect molecule that discharges to be called as " releasing factor ".In certain embodiments, the advantage of releasing factor is to have anti-tumor activity simultaneously.

The releasing factor of being expressed by bacteria carrier of the present invention can be the castle's intrinsic factor of the attenuated bacteria that is oriented to tumor after modifying, and also can be exogenous factor (for example a kind of nucleic acid that itself is not had by the attenuated bacteria that is oriented to tumor is encoded).Releasing factor can be encoded by nucleic acid such as plasmids, also can be encoded by the nucleic acid that is incorporated in the attenuated bacteria genome that is oriented to tumor.Releasing factor can be encoded by the same nucleic acid or the plasmid of coding primary effector molecule, also can be encoded by different nucleic acid or plasmid.Releasing factor can be encoded by the same nucleic acid or the plasmid of coding second order effect molecule, also can be encoded by different nucleic acid or plasmid.In an embodiment, the expression of releasing factor is to carry out in a kind of cell, and this cell can also be expressed a kind of primary effector molecule and proteic fusion rotein of Omp sample of containing.In this embodiment, the coexpression of releasing factor can promote this fusion rotein to discharge from periplasmic space.

In a preferred embodiment, the releasing factor of using discharges albumen as bacteriocin, or BRPs (after this being called BRP in classification).The BRP that the present invention uses can be from any source known in the art, comprising, but be not limited to cloacin DF13 plasmid, colicine E1-E9 plasmid, or colicine A, N or D plasmid.In a preferred embodiment, the BRP of use is from cloacin DF13 (pCloDF13 BRP).

BRPs is generally 45-52 amino acid whose peptide, and initial synthetic is precursor molecule (PreBRP), wherein contains the signal sequence of not sheared by the signal endopeptidase.The activity of BRP has at least a part to be mediated by detergent resistance adventitia phospholipase A (PldA), (summary of relevant BRPs can be with reference to van der Walet al. in the reinforcement that this activity is degraded with outer membrane phospholipid usually, 1995, FEMS Microbiology Review 17:381-399).Under the prerequisite that is not subjected to the principle restriction, BRP can promote the pericentral siphon composition preferentially to discharge, but the kytoplasm composition that also can detect than low degree discharges.When BRP is crossed expression by appropriateness, can make bacterial membrane become fragile, thereby cause the height of accurate cracking state and kytoplasm composition to discharge.In addition, when BRP is flatly crossed expression by superelevation, can cause bacteria cell cracking, so just can discharge the delivery of cells content by cracking.In this embodiment, the expression of BRP can be associated with BRP activity (as the release of antibacterial content).For example, the BRP activity of superelevation level can cause nearly all bacteria cell cracking.Therefore, " expression of superelevation level " used in the literary composition is defined as causing nearly all antibacterial that cracked BRP expression takes place.Compare with the contrast bacterium of not expressing BRP, the BRP activity of appropriateness can discharge with the part of antibacterial content or discharge to be strengthened, but does not cause the antibacterial cracking.Therefore, in this embodiment, the appropriateness of BRP is crossed to express and is defined as strengthening the kytoplasm composition and discharges but can not cause nearly all antibacterial that cracked expression takes place." nearly all antibacterial " of using in the literary composition is meant the antibacterial more than 60%, the antibacterial more than 70% preferably, the antibacterial more than 80% more preferably, the more preferably antibacterial more than 90%, the most preferably antibacterial of 90-100% again.

In a special embodiment of the present invention, the BRP albumen that uses is the pCloDF13BRP mutant, the cracking function of this mutant with albumen release function uncoupling, thereby can not cause strengthening proteic release (van der Wal et al. under the cracked situation of antibacterial, 1998, App.Env.Microbiol.64:392-398).The albumen that this embodiment can prolong bacteria carrier discharges, and can reduce the requirement with the carrier frequent drug administration simultaneously.In another special embodiment, BRP of the present invention is the pCloDF13 BRP that C-end shortens, and this BRP can cause that not only albumen discharges, can also cause lysis (Luirink et al., 1989, J.Bacteriol.171:2673-2679).

In another embodiment of the present invention, the enhancing delivery system of use comprises a kind of expression of crossing of porin; Can reference, for example, Sugawara, E.and Nikaido, H., 1992, J.Biol.Chem.267:2507-11.

In certain embodiments, when BRP is when being expressed by bacteria carrier of the present invention, this BRP can be the endogenous molecule of the attenuated bacteria that is oriented to tumor after modifying, and also can be exogenous molecules (for example a kind of nucleic acid that itself is not had by the attenuated bacteria that is oriented to tumor is encoded).BRP can be encoded by nucleic acid such as plasmids, also can be encoded by the nucleic acid that is incorporated in the attenuated bacteria genome that is oriented to tumor.BRP can be encoded by the same nucleic acid or the plasmid of coding primary effector molecule, also can be encoded by different nucleic acid or plasmid.BRP can be encoded by the same nucleic acid or the plasmid of coding second order effect molecule, also can be encoded by different nucleic acid or plasmid.In an embodiment, the proteic expression of BRP sample is to carry out in a kind of cell, and this cell can also be expressed a kind of effector molecule and proteic fusion rotein of Omp sample of containing.In this embodiment, the coexpression of BRP can promote the release of this fusion rotein.

In a particularly preferred embodiment of the present invention, the code nucleic acid of BRP is to be encoded by a kind of colicine plasmid.In another special embodiment of the present invention, the expression of BRP code nucleic acid is to carry out under the regulation and control of natural B RP promoter, this promoter be a kind of can be in normal host (the normal host of BRP, the cloaca enterococcus) the SOS promoter that stressed condition (for example ultraviolet light etc. can cause the condition of DNA damage) is reacted, and also be part constitutive promoter in the Salmonella.In a preferred embodiment, the expression of BRP code nucleic acid is to carry out under the regulation and control of pepT promoter, and this promoter can react on the anaerobic character of tumor environment and the (reference that is activated, for example, Lombardo et al., 1997, J.Bacteriol.179:1909-17).

As selection, the promoter of use also can be the antibiotic inducible promoter, as the tet promoter of Tn10 transposon.In a preferred embodiment, the tet promoter of using is monomeric form, and this monomer can be to tetracycline or its analog that exists, as doxycycline and anhydrotetracycline, produce the reaction of all or none, thereby can form a kind of on-off switch with hereditary stability.In another embodiment, the tet promoter of use is many bodily forms formula, for example the trisome form.This many bodies promoter can produce fractionated reaction to the tetracycline that exists, thereby can form a kind of system that has more operability that is used for the control effect molecular level.After utilizing the attenuated bacteria that is oriented to tumor of the present invention that the experimenter is handled, the tetracycline of suitable dosage can be delivered medicine to this experimenter, with the activity of evoked promoter.The initial tet inducible expression system of describing is to be used for pombe fission yeast (Faryar and Gatz, 1992, Current Genetics 21:345-349) eukaryotic system and mammalian cell (Langand Feingold such as, 1996, and nearest research makes its suitability expand to bacterial cell Gene 168:169-171).For example, people such as Stieger (1999, Gene 226:243-252) prove, when the Lampyridea luciferase genes with after tet promoter operability is connected, can induce by tet and obtain 80 times inducing action.The advantage of this promoter is that it can be induced under extremely low tetracycline level, this level is about 1/10th of antibiotic activity required dosage.5.4. Derivant and analog

The present invention comprises that also these derivants include, but are not limited to through processing codified or send a kind of bacteria carrier of derivant, primary effector molecule and (or) fragment, analog or the variant of second order effect molecule or its code nucleic acid.These derivants, analog or variant have functional activity, for example can show one or more functional activities of total length wild type effector molecule.This derivant, analog or variant with expection treatment characteristic can be used for, and for example, suppresses the diffusion (transfer) of growth of tumor or tumor cell.Utilize methods known in the art, comprise method described herein, can measure the derivant of required effector molecule or the activity of analog.

In detail, the preparation method of variant can be by replacing, add (as inserting) or removing the coded sequence that changes effector molecule, the gained molecule to be compared with the wild type effector molecule had identical or higher anti-tumor function.For example, variant of the present invention comprises, but be not limited to, the all or part of aminoacid sequence that contains a kind of effector molecule in the one-level aminoacid sequence, and those molecules that contain the sequence that changes in this aminoacid sequence, the residue that changes sequence is replaced by the reticent amino acid residue that changes that causes in sequence of equal value on the function, promptly is changed sequence and contains conservative a replacement at least.

Utilize methods known in the art can make any code nucleic acid that derives from mammiferous primary effector molecule or second order effect molecule adopt the codon of antibacterial through processing.The example that preferred codon uses is seen Current Protocols in Molecular Biology, GreenPublishing Associates, Inc., and John Wiley ﹠amp; Sons, Inc.NewYork and Zhang et al., 1991, Gene 105:61-72.

In a special embodiment, the derivant of primary effector molecule or second order effect molecule, analog or variant contain a kind of nucleotide sequence, this sequence can with coding primary effector molecule or second order effect molecule or its segmental nucleotide sequence hybridization, hybridization conditions is a stringent condition, for example in 6 about 45 ℃ * sodium chloride/sodium citrate (SSC), hybridize with the DNA that is attached on the filter membrane, in 0.2 * SSC/0.1%SDS of about 50-65 ℃, clean one or many then, or height stringent condition, for example in 6 about 45 ℃ * SSC be attached to nucleic acid hybridization on the filter membrane, in 0.1 about 68 ℃ * SSC/0.2%SDS, clean one or many then, or other stringent hybridization conditions well known by persons skilled in the art (can reference, for example, Ausubel, F.M.et al., eds., 1989, Current Protocols inMolecular Biology, Vol.I, Green Publishing Associates, Inc.and John Wiley ﹠amp; Sons, Inc., 6.3.1-6.3.6 page or leaf and the 2.10.3 page or leaf of New York).

The derivant or the analog of primary effector molecule or second order effect molecule comprise, but be not limited to, contain with the molecule in primary effector molecule or second order effect molecule or the homologous substantially zone of its fragment (for example, in different embodiments, compare with the aminoacid sequence of the equal length that does not contain any insertion or disappearance, or with the contrast sequence compare, has 60% or 70% or 80% or 90% or 95% homogeneity at least, contrast wherein is to be finished by computer homology comparison program known in the art), or its code nucleic acid can be at the height stringent condition, the molecule of hybridizing with the proteic effector molecule coded sequence of a kind of effector molecule under moderate stringent condition or the low stringent condition.

In order to determine the homogeneity percentage rate of two seed amino acid sequences or two kinds of nucleotide sequences, homogeneity percentage rate between for example a kind of primary effector molecule sequence and another kind of known array, two kinds of sequences can be compared, to obtain optimum comparative result (for example can in the first seed amino acid sequence or nucleotide sequence, introduce the room) with the optimum contrast of acquisition with the second seed amino acid sequence or nucleotide sequence.Amino acid residue or nucleotide with corresponding amino acid position or corresponding nucleotide position compares then.Is when being occupied by identical amino acid residue or nucleotide when position of first kind of sequence with the correspondence position of second kind of sequence, and these two kinds of molecules are identical in this position.Homogeneity percentage rate between two kinds of sequences is the function (that is total quantity * 100 of the quantity/position of homogeneity percentage rate=same position (as the lap position)) of the total same position quantity of these two kinds of sequences.In an embodiment, the length of these two kinds of sequences is identical.

Homogeneity percentage rate between two kinds of sequences can be determined with a kind of mathematical algorithm.A non-limiting preferred embodiment that can be used to the mathematical algorithm of two kinds of sequences of comparison is Karlin andAltschul, 1990, the algorithm that Proc.Natl.Acad.Sci.USA 87:2264-2268 describes, at Karlin and Altschul, 1993, among the Proc.Natl.Acad.Sci.USA 90:5873-5877 this algorithm is revised.This algorithm is integrated into Altschul, et al., and 1990, among the NBLAST and XBLAST program that J.Mol.Biol.215:403-410 describes.With scoring=100, word length=12 is that parameter is carried out the BLAST nucleotide search with the NBLAST program, can obtain and the homologous nucleotide sequence of nucleic acid molecules of the present invention.With scoring=50, word length=3 is that parameter is carried out the search of BLAST albumen with the XBLAST program, can obtain and the homologous aminoacid sequence of protein molecular of the present invention.For obtain to have vacant position to recently comparing, can be by Altschul et al., 1997, the described use of Nucleic Acids Res.25:3389-3402 Gapped blast program.As selection, also can carry out iterative search, with the distance relation between detection molecules (Id.) with the PSI-Blast program.When using BLAST, Gapped BLAST and PSI-Blast program, can adopt these programs (as XBLAST and NBLAST) default parameters separately.See http://www.ncbi.nlm.nih.gov.Another the non-limiting preferred embodiment that can be used for the mathematical algorithm of sequence comparison is Myers and Miller, the algorithm that CABIOS (1989) describes.This algorithm is integrated in the ALIGN program (2.0 version), and this program is the part of GCG sequence comparison software bag.When utilizing the ALIGN program to carry out the aminoacid sequence comparison, can adopt PAM120 weight residue table, and room length point penalty is made as 12, gap penalty is made as 4.Other algorithms that are used for sequence analysis are well-known in the art, comprising Torellis and Robotti, 1994, Comput.Appl.Biosci., ADVANCE that describes among the 10:3-5 and ADAM; And Pearson and Lipman, 1988, the FASTA that describes among the Proc.Natl.Acad.Sci.85:2444-8.In the FASTA program, ktup is a control option, and this option can be provided with the sensitivity and the speed of search.If ktup=2 then is by seeking the contrast residue to finding two kinds of similar areas in the comparative sequences; If ktup=1 then is the aminoacid that detects single arrangement.Ktup can be made as 2 or 1 when comparing protein sequence, can be made as 1-6 during the comparison dna sequence.If do not set, then relatively the acquiescence ktup of protein sequence is 2, and the acquiescence ktup of comparison dna sequence is 6.Other descriptions of relevant FASTA program can be with reference to http://bioweb.pasteur.fr/docs/man/man/fasta.1.thml#sect2, and its content is hereby incorporated by.

As selection, can also use Higgins et al., 1996, the CLUSTAL W algorithm that Methods Enzymol.266:383-402 describes carries out protein sequence relatively.

Homogeneity percentage rate between two kinds of sequences can be with being similar to permission room mentioned above or not allowing the technology in room to determine.When calculating the homogeneity percentage rate, only calculate the situation of coupling fully.

Primary effector molecule or second order effect molecule, or derivatives thereof or analog can produce by distinct methods known in the art.The operation that can produce these molecules can be carried out on nucleic acid level, also can carry out on protein level.For instance, can be right with multiple strategy known in the art, for example, the coding for example a kind of a kind of clone's of effector molecule effector molecule coded sequence modify (Sambrook et al., 1989, Molecular Cloning, ALaboratory Manual, 2nd ed., Cold Spring Harbor LaboratoryPress, Cold Spring Harbor, New York).Can with restriction endonuclease sequence be sheared at suitable position, if desired, can also carry out other enzymatically modifying, separate then with external and be connected.When the modified model effector molecule of derivant that produces a kind of codified primary effector molecule or second order effect molecule or analog, the coded sequence that should note guaranteeing the modified model effector molecule still can keep the translation frame identical with native protein in the effector molecule coded sequence district of required primary effector molecule of coding or second order effect molecular activity, and is not translated termination signal and interrupts.

Can carry out external or vivo mutations to the nucleotide sequence of coded actions molecule in addition, with produce and (or) destroy translation sequences, homing sequence and (or) terminator sequence, or generation variation in the coding region, and (perhaps) form new or destroy original restriction endonuclease site, thereby help other external modifications.In a particularly preferred embodiment, a kind of nucleic acid sequence encoding of effector molecule is passable through sudden change, for example, produces a kind of more effective variant.Any induced-mutation technique known in the art all can use, comprising, but be not limited to, chemomorphosis, external direct mutagenesis (Hutchins on et al., 1978, J.Biol.Chem.253:6551), use TAB  joint (Pharmacia), carry out PCR with the primer that contains sudden change, or the like.In a preferred embodiment, the non essential amino acid residue to a kind of one or more predictions of effector molecule has carried out the conserved amino acid replacement." conserved amino acid replacement " is meant, amino acid residue replaced to the amino acid residue that a kind of institute band side chain has similar electric charge.This area defines the amino acid residue family that institute's band side chain has a similar electric charge.These families comprise that the aminoacid that has basic side chain is (as lysine, arginine, histidine), the aminoacid that has acid side-chain is (as aspartic acid, glutamic acid), the aminoacid that has uncharged polar side chain is (as glycine, agedoite, glutamine, serine, threonine, tyrosine, cysteine), the aminoacid that has non-polar sidechain is (as alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), the aminoacid that has the β branched building block is (as threonine, valine, isoleucine) and the aminoacid that has an aromatic series side chain (as tyrosine, phenylalanine, tryptophan, histidine).As selection, also can pass through, for example, the saturation mutagenesis method is introduced sudden change at random in all or part of coded sequence, and the biological activity to the gained mutant screens then, still has active mutant to identify.After mutation is finished, can express encoded protein, and measure this proteic activity.

In another embodiment, effector molecule of the present invention or fusion rotein contain a kind of protease cutting site through making up.5.5. Fusion rotein

In certain embodiments, the invention provides primary effector molecule or the second order effect molecule that makes up with the form of fusion rotein (for example with a kind of different albumen covalent bond).The invention provides the code nucleic acid of these fusion rotein.In some other embodiment of the present invention, fusion rotein code nucleic acid of the present invention is connected with a kind of suitable promoter operability.

In a special embodiment, effector molecule is built into a kind of chimeric protein or fusion rotein, this albumen contains a kind of effector molecule or its fragment (preferably is made up of at least a domain or the motif of this effector molecule, or by at least 5, at least 10, at least 25, at least 50, at least 75 of this effector molecule, or at least 100 aminoacid are formed), and by peptide bond at effector molecule or its segmental aminoterminal or c-terminus and a kind of different proteic aminoacid sequences connections.In a particularly embodiment, fusion rotein contains a kind of heterologous polypeptide or its segmental at least 2, at least 6, at least 10, at least 20, at least 30, at least 50, at least 75 of active function or at least 100 continuous amino acids.In an embodiment, the production method of this fusion rotein or chimeric protein is that the code nucleic acid (as TNF-coded sequence, anti-angiogenesis coded sequence, tumor suppression enzyme coded sequence, or cytotoxicity polypeptid coding sequence) of the primary effector molecule that will connect by frame with a kind of different proteic coded sequences carries out recombinant expressed.The preparation method of this chimeric product can be, utilize will the encode suitable nucleotide sequence of amino acid needed sequence of methods known in the art to be connected to each other, and utilize method well-known in the art in selected expression vector, to express this chimeric product by suitable reading frame.The chimeric nucleic acid that makes up can contain the part code nucleic acid of a kind of effector molecule that merges with any heterologous polypeptide coded sequence.There is a special embodiment to relate to a kind of chimeric protein, this albumen contains primary effector molecule or second order effect molecule at least 5, at least 10, at least 25, at least 50, or at least 100 amino acid whose a kind of fragments, or contain a kind of fragment that shows one or more functional activities of total length primary effector molecule or total length second order effect molecule.

In a special embodiment, the fusion rotein of use contains a kind of affinity labeling, as six polyhistidine tags or be used for purification, separation, evaluation or express other affinity labelings of measuring.In another special embodiment, fusion rotein contains a kind of protease cutting site, as metalloprotein enzyme action site or serine enzyme action site.In this embodiment, preferably in fusion rotein of the present invention, make up a kind of corresponding restriction enzyme site that can have active protease sometimes at tumor locus.In some embodiments, be (as signal sequence, targeting sequencing, pericentral siphon district, membrane spaning domain, multispan membrane structure territory with effector molecule and a kind of Omp sample albumen or its fragment, or its combination, the 3.1st joint that sees above is to the definition of " Omp sample albumen ") be built into a kind of fusion rotein.

In a preferred embodiment, effector molecule of the present invention (elementary or secondary) is the formal representation that has the fusion rotein of outer membrane protein (Omp sample albumen) with a kind of.Bacterial outer membrane albumen is the conformity membrane albumen of bacterial outer membrane, and this albumen has multispan membrane structure territory, and often is connected with one or more fat parts.Initial outer membrane protein of expressing is the precursor forms (pro-Omp) that contains the aminoterminal signal peptide, and this signal peptide can be sheared the albumen oriented film on film then by signal peptidase, thereby produces maturation protein.In an embodiment, be that effector molecule and a kind of Omp sample albumen are built into a kind of fusion rotein.In this embodiment, primary effector molecule is reinforced to sending of bacterial outer membrane.Although do not wish to be subjected to the restriction of principle, the inventor thinks that Omp sample albumen can be used as a kind of deadman between effector molecule and the adventitia or connects thing, or can be used to make effector molecule to be positioned bacterial outer membrane.In an embodiment, effector molecule and the proteic fusion rotein of Omp sample are used to the accelerating effect molecule and are positioned pericentral siphon.In another embodiment, effector molecule and the proteic fusion rotein of Omp sample are used to the release of accelerating effect molecule.In a particularly embodiment, the Omp sample albumen that uses contains OmpA, OmpB, OmpC, OmpD, OmpE, OmpF, OmpT, porin sample albumen, PhoA, PhoE, lamB, beta-lactamase, a kind of enterotoxin, protein A, endoglucanase, the relevant lipoprotein (PAL) of Peptidoglycan, FepA, FhuA, NmpA, NmpB, NmpC at least, or the part of a kind of main outer membrane lipoprotein (as LPP) etc.In certain embodiments of the invention, the signal sequence of structure has stronger hydrophobicity (aminoacid replacement that for example inserts or incite somebody to action wherein becomes hydrophobic amino acid, as leucine) in signal sequence.The 7.1-7.4 joint that illustrative embodiment sees below.

In another embodiment of the present invention, fusion rotein of the present invention contains a kind of Proteolytic enzyme shearing site.This Proteolytic enzyme shearing site can be the endogenous site of effector molecule, also can be the proteic endogenous site of Omp sample, can also be the Proteolytic enzyme shearing site that is building up in the fusion rotein.In certain embodiments, Omp sample albumen of the present invention is the heterozygosis Omp that contains from the proteic structural detail of difference.

In embodiment as an example, Omp sample albumen is OmpA; The principle that makes up OmpA sample fusion rotein is applicable to other Omp fusion rotein too, but will note the proteic configuration of specific Omp sample.

For example, natural OmpA albumen contains 8 antiparallels and strides the film beta chain in its 170 amino acid whose N-end protein domains.Be extracellular loop or cell internal ring between every pair of membrane spaning domain, this depends on the direction of insertion of membrane spaning domain.The C-end structure territory of being made up of 155 aminoacid is positioned at cell, and may contact with the Peptidoglycan that is full of periplasmic space.Obtained to be beneficial to generation OmpA Expression of Fusion Protein carrier at present.For example, people such as Hobom (1995, Dev.Biol.Strand.84:255-262) developed a kind of carrier, this carrier contains the OmpA open reading frame, and in the coded sequence of the 3rd or the 4th extracellular loop, inserted joint, thereby can insert selected heterologous protein by frame.

In an embodiment of the present invention, the expression of primary effector molecule part in pericentral siphon that contain of OmpA fusion rotein strengthened.In the one side of this embodiment, ripe preceding fusion rotein is held the signal sequence that contains signal sequence or connected an OmpA membrane spaning domain at least at primary effector molecule N-.Signal sequence is cut, thereby maturation protein does not contain signal sequence.At this embodiment on the other hand, primary effector molecule is positioned at the N-end of OmpA fusion rotein, as long as fusion rotein has stability, can change the OmpA membrane spaning domain quantity of use, and this can not exert an influence to the location of primary effector molecule.At this embodiment on the other hand, primary effector molecule is between the N-of OmpA end structure territory and C-end structure territory, and this fusion rotein by after the shearing of periplasm protein enzyme, can form the solubility periplasm protein that contains primary effector molecule in pericentral siphon.In some mode of this embodiment, preferably express the bacteria carrier of pericentral siphon primary effector molecule and can also express BRP simultaneously, thereby can promote bacterial cell release effects molecule.

In another embodiment of the present invention, the part that the OmpA fusion rotein contains primary effector molecule is positioned at the cell outer surface of antibacterial.In aspect of this embodiment, fusion rotein contains odd number or even number OmpA membrane spaning domain at the N-of primary effector molecule end.On the other hand, primary effector molecule thereby can be presented to tumor cell by antibacterial between two extracellular loop of OmpA.In a particularly embodiment, the invention provides expression plasmid at antibacterial outer surface expression effect molecule fusion protein.For example, the plasmid that is called as Trc (lpp) ompA contains and the trc promoters driven strides fat polypeptide (lpp) the anchor sequence that the film sequence merges with truncate ompA.Another example is the plasmid that is called as TrcompA, and this plasmid contains the ompA coded signal sequence of trc promoters driven.These plasmids are through making up the nucleic acid that can contain a kind of one or more effector molecules of the present invention of encoding.

As selection, can also be before effector molecule or the effector molecule flank make up some and can be present in the metalloproteases in the tumor or the total shearing site of serine protease identification in a large number, be used for this effector molecule is discharged into tumor environment.Protease cutting site is to depend on that respectively this effector molecule is at the end of fusion rotein or in the inside of fusion rotein before primary effector molecule or at the primary effector molecule flank.

According to the above-mentioned strategy that is used for OmpA, can construct similar fusion rotein with any Omp sample albumen.When making up this fusion rotein, those of ordinary skill in the art understands, and what the proteic effector molecule of Omp sample merged that selection partly depends on this effector molecule needs expressive site (as pericentral siphon, extracellular, combine with film, or the like).The construction method of relevant primary effector molecule fusion rotein described herein is applicable to the second order effect molecule too.

In a preferred embodiment, effector molecule is to merge with a kind of peptide that transports.Studies show that, in fusion rotein, use transport peptide help with nearly all cell to the range of scatter that is in its generation or introducing of desired polypeptides or delivery of peptides (can reference, for example, Bayley, 1999, Nature Biotechnology 17:1066-1067; Fernandez et al., 1998, Nature Biotechnology 16:418-420; With Derossi et al., 1998, Trends Cell Biol.8:84-87).Therefore, the attenuated bacteria that is oriented to tumor is processed into expresses the method that contains the fusion rotein that transports peptide and effector molecule and can improve effector molecule by the ability of tumor cell internalization.In a special embodiment, the attenuated bacteria that is oriented to tumor can be expressed a kind of nucleic acid molecules, a kind of fusion rotein that transports peptide and effector molecule that contains of this nucleic acid molecules codified through processing.In another embodiment, the attenuated bacteria that is oriented to tumor can be expressed one or more nucleic acid molecules through processing, and one or more contain the fusion rotein that transports peptide and effector molecule these nucleic acid molecules codifieds.Effector molecule in these embodiments can be a primary effector molecule, also can be the second order effect molecule.The example that transports peptide comprises, but be not limited to, derive from the proteic peptide of HIV TAT, feeler foot homeodomain (penetrating albumen), Ka Boxi fibroblast growth factor (FGF) membrane translocation sequence (MTS), herpes simplex virus VP22, poly histidine (as six polyhistidyls; 6H), poly-D-lysine is (as six polylysines; 6K), and the poly arginine (as six poly arginines; 6R) (reference, for example, Blanke et al., 1996, Proc.Natl.Acad.Sci.USA 93:8437-8442).

In another preferred embodiment, fusion rotein contains a kind of signal peptide, a kind of peptide and a kind of effector molecule of transporting.In this embodiment, a kind of mode is that the attenuated bacteria that is oriented to tumor can be expressed one or more nucleic acid molecules through processing, and one or more contain these nucleic acid molecules codifieds signal sequence, transport the fusion rotein of peptide and effector molecule.In the embodiment of this mode, effector molecule can be a primary effector molecule, also can be the second order effect molecule.

In another preferred embodiment, can will contain a kind of signal peptide, a kind of Proteolytic enzyme shearing site, a kind of fusion rotein that transports peptide and a kind of effector molecule by the attenuated bacteria that is oriented to tumor and be delivered to solid tumor.In a special embodiment, the attenuated bacteria that is oriented to tumor can be expressed one or more nucleic acid molecules through processing, and one or more contain these nucleic acid molecules codifieds signal sequence, Proteolytic enzyme shearing site, transport the fusion rotein of peptide and effector molecule.Effector molecule in this embodiment can be a primary effector molecule, also can be the second order effect molecule.

In a non-limiting example, be to improve the activity of colicine by the peptide that derives from HIV TAT, herpes simplex virus VP22, feeler foot homeodomain, 6H, 6K and 6R in interpolation.Can be C-end, N-end or inner the fusion.The inside of fusion position set after N-end signal sequence is sheared peptide is merged preferred especially.This fusion rotein also can contain C-end signal sequences such as N-end signal sequences such as OmpA or hlyA in addition.

In a preferred embodiment, effector molecule and a kind of toxin sends partial fusion.Known have multiple toxin to have autonomous delivery capability, and some can be used as the delivery agents of another part in these toxin.For example, Ballard et al., 1996, Proc.Natl.Acad.Sci.USA 93:12531-12534 proves, anthrax protective agent (PA) can mediate the cytosolic space that lethal factor (LF) and edema factor enter mammalian cell, can also mediate the LF (LFn with clipped form; 255 amino acid residues) proteic the entering of Rong Heing.Therefore, except the effector molecule of extracellular performance function, effector molecule of the present invention can merge with LFn or other toxin systems, comprising, but be not limited to, 1-193 residue (the Blanke et al. of diphtheria toxin, diphtherotoxin A chain, 1996, Proc.Natl.Acad.Sci.USA93:8437-8442), cholera toxin, the Vero cytotoxin, escherichia coli heat-labile toxin (LTs), escherichia coli heat-stable toxin (STs), the enteric sanguinin, enterotoxin, cytotoxin, EAggEC ST 1 (EAST), CNFs, cell lethality expansion toxin, alpha hemolysin, beta hemolysin, and the SheA hemolysin (relevant summary can reference, for example, O ' Brienand Holmes, 1996, Protein toxins of Escherichia coli andSalmonella.Cellular and Molecular Biology, Neidhardt et al. (eds), ASM Press, Washington, D.C., pp2788-2802).In a special embodiment, be the partial fusion of sending with primary effector molecule and a kind of toxin.In another special embodiment, be the partial fusion of sending with second order effect molecule and a kind of toxin.

The construction method of the fusion rotein of expressing in antibacterial is well-known in the art, and these methods are all located within the scope of the invention.(reference, for example, Makrides, S., 1996, Microbiol.Revs 60:512-538 is this complete being incorporated herein by reference) 5.6. Expression vector

The invention provides some through processing and encode one or more primary effector molecules and the optional attenuated bacteria that is oriented to tumor of one or more second order effect molecules.The invention provides the attenuated bacteria that is oriented to tumor that some contain effector molecule, but these effector molecules are by plasmid or transfection nucleic acid coding.In a preferred embodiment of the present invention, the attenuated bacteria that is oriented to tumor that uses is Salmonella.When the attenuated bacteria that is oriented to tumor when Salmonella etc. can be expressed more than one effector molecule (as elementary effector molecule or second order effect molecule); these effector molecules can be encoded by identical plasmid or nucleic acid, also can be encoded by more than one plasmid or nucleic acid.The present invention also provides some to contain the attenuated bacteria that is oriented to tumor of effector molecule, and these effector molecules are by the nucleic acid molecule encoding that is incorporated in the bacterial genomes.The effector molecule of integrating can be the endogenous molecule that Salmonella etc. is oriented to the attenuated bacteria of tumor, also can be introduced in the attenuated bacteria that is oriented to tumor and (for example introduce a kind of nucleic acid of codified effector molecule, but as plasmid transfection nucleic acid, transposon, or the like), make this nucleic acid molecules of coded actions molecule can be incorporated in the genome of the attenuated bacteria that is oriented to tumor.In a preferred embodiment of the present invention, the attenuated bacteria that is oriented to tumor that uses is Salmonella.The invention provides a kind of and the suitable nucleic acid molecules of the codified effector molecule that is connected of promoter operability.The promoter that is connected with the nucleic acid operability of coded actions molecule can be homologous (promptly own), also can be allogenic (nucleic acid itself that is the coded actions molecule does not have).

The nucleotide sequence of effector molecule of the present invention or its functional activity analog or fragment or other derivants of encoding can be inserted in a kind of suitable expression, for example contains the plasmid of the necessary element of albumen coded sequence of transcribing or translate insertion.The essential signal of transcribing or translating can by effector molecule and (or) its flank region provides.As selection, the construction method of expression vector can also be, utilizes multiple DNA operational approach known in the art to be inserted in the functional promoter at exercisable will the encode structural DNA sequence of destination protein and suitable translation initiation signal and the termination signal of yard stage of reading.Usually can be with reference to Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2nd ed., Cold SpringHarbor Laboratory Press, Cold Spring Harbor, NY; Ausubel etal., 1995, Current Protocols in Molecular Biology, GreenPublishing, New York, NY.These methods can comprise reorganization (genetic recombination) method in DNA vitro recombination and synthetic technology and the body.The invention provides a kind of and the suitable nucleic acid molecules of the codified effector molecule that is connected of promoter operability.

The present invention also provides some through processing and encode one or more fusion rotein and the optional attenuated bacteria that is oriented to tumor of one or more effector molecules.The invention provides the attenuated bacteria that is oriented to tumor that some contain fusion rotein, but these fusion rotein are by plasmid or transfection nucleic acid coding.The attenuated bacteria that is oriented to tumor when Salmonella etc. can express more than one fusion rotein and (or) during effector molecule (as elementary effector molecule or second order effect molecule); these fusion rotein with (or) effector molecule can be encoded by identical plasmid or nucleic acid, also can be encoded by more than one plasmid or nucleic acid.The present invention also provides some to contain the attenuated bacteria that is oriented to tumor of fusion rotein, and these fusion rotein are by the nucleic acid coding that is incorporated in the bacterial genomes.The present invention also provides a kind of and the suitable nucleic acid molecules of the codified fusion rotein that is connected of promoter operability.The nucleotide sequence of fusion rotein of the present invention of encoding can be inserted in a kind of suitable expression, for example contains the plasmid of the necessary element of albumen coded sequence of transcribing or translate insertion.

In some special embodiment of the present invention, expression vector of the present invention is a kind of plasmid.Have a large amount of plasmids to be suitable for producing recombinant precursor of the present invention, these plasmids are understood by those skilled in the art, and can obtain with commercial form.

Above-mentioned commercialization plasmid comprises, for example, pKK223-3 (Pharmacia FineChemicals, Uppsala, Sweden) and GEM1 (Promega Biotec, Madison, WI, USA).These plasmids combine pBR322 " main chain " part with a kind of suitable promoter and the structure sequence that will express.PBR322 is considered to a kind of plasmid of low copy number.If obtain high-caliber expression, can adopt the plasmid of high copy number, as contain the plasmid of pUC main chain.The pUC plasmid includes, but are not limited to, pUC19 (reference, for example, Yanisch-Perron et al., 1985, Gene 33:103-119) and pBluescript (Stratagene).

The following plasmid that provides as example can use with method of the present invention is collaborative.Antibacterial: pBs, phagescript, phiX174, pbluescript SK, pBs KS, pNH8a, pNH16a, pNH18a, pNH46a (Stratagene); PTrc99A, pKK223-3, pKK233-3, pDR540, pRIT5 (Pharmacia).Also can use the commercialization plasmid that contains pBR322 " main chain ", as pKK223-3 (Pharmacia Fine Chemicals, Uppsala, Sweden) and GEM1 (Promega Biotec, Madison, WI, USA).These plasmids can combine with suitable promoter and the structure sequence that will express.PCET, pTS (as described in this paper the 6th joint).

In special embodiment of the present invention, the plasmid of coded actions molecule is pTS-TNF-α plasmid, pTS-BRP plasmid or pTS-BRPTNF-α plasmid, and this paper the 6th joint is seen in the description of relevant these plasmids.

In a special embodiment of the present invention, the fusion rotein of the present invention that contains OmpA signal sequence and primary effector molecule that is used to be secreted into periplasmic space is plasmid-encoded by pIN-III-ompA-Hind, this plasmid contains the dna encoding sequence of ompA signal sequence, and this sequence is positioned at the upstream of the joint sequence that can clone the primary effector molecule coded sequence.In a particularly preferred embodiment, the lac inducible promoter of pIN-III-ompA-Hind carrier is replaced by pepT or tet promoter (with reference to Rentier-Delrue et al., (1988), Nuc.Acids Res.16:8726).

The present invention also provides the pairing effect molecule to carry out the method for transposon-mediated chromosomal integration.As long as the code nucleic acid of effector molecule can be building up in the transposon box, any transposon plasmid known in the art can use in the method for the invention.For example, the invention provides a kind of transposon plasmid, this plasmid contains a kind of transposon or little transposon and MCS.

In certain embodiments of the invention, plasmid of the present invention is a kind of transposon plasmid, that is to say, this plasmid contains a kind of transposon, has wherein inserted the coded sequence of purpose effector molecule.The transposon plasmid contains the transposon box, and these transposon boxes can be incorporated in the bacterial genomes.Therefore, the code nucleic acid of effector molecule or its fusion rotein can be inserted in the transposon box.So just can the transposon insertion sequence be incorporated in the bacterial genomes by the transposon box.The coded sequence of effector molecule can be connected with a kind of promoter operability, also can not contain promoter.When not containing promoter, the bacterial genomes promoters driven at position is inserted in the expression of selectable marker by transposon.The bacterial clump that contains the transposon insertion sequence is screened,, for example be enough to promote the cytotoxicity of tumor, the cytokine-expressing level of smouldering or degenerating to obtain to satisfy the expression of requirement of the present invention.

In certain embodiments, the transposon plasmid that uses is except that containing transposon, but also outside the reverse duplicate block of transposon, contain the transposase gene in a kind of catalysis transposon insertion bacterial genomes, but this gene can together not insert with transposon, has the bacterial isolates of stablizing the transposon insertion sequence thereby can produce.

Can include, but are not limited to Tn7, Tn9, Tn10 and Tn5 for the transposon that the present invention uses.In a preferred embodiment, the transposon plasmid that uses is pNK2883 (ATCC), this plasmid contains ampicillin resistance gene outside the Tn10 insertion element, and (in the transposon box) contains the code nucleic acid of one or more effector molecules between two Tn10 insertion elements.Preferably, when the preparation construct, the additional sequences of other elements of coding can also be inserted between two Tn10 insertion elements.In a particularly embodiment, these elements optionally comprise the no promoter copy (as SerC, AroA, or the like) of (1) selectable marker, are used to screen the positive bacteria that contains plasmid; (2) a kind of BRP gene; (3) be suitable for a kind of promoter (as trc) that effector molecule uses, the code nucleic acid operability of this promoter and one or more primary effector molecules (as TNF-α or its fusion rotein, as the OmpA-TNF-alpha fusion protein) connects; (4) be suitable for a kind of terminator that the code nucleic acid of one or more effector molecules uses.

In an embodiment, when plasmid being carried out proper handling and utilizing after plasmid-encoded amicillin resistance feature filters out the clone who contains required construct, can remove antibiotic-screening by the forfeiture of plasmid, select the bacterial strain (as being tiled on the selection culture medium) that contains chromosome transposon insertion sequence then, be used for administration to the human experimenter.

Another special embodiment is to adopt the pTS plasmid, and this plasmid contains the different transposase gene of a kind of target-specific and a kind of little transposon, and this little transposon contains the coded sequence that has or not promoter serC gene and MCS.Another special embodiment is to adopt the pTS-BRP plasmid, this plasmid contains the different transposase gene of a kind of target-specific and a kind of little transposon, and this little transposon contains the coded sequence that has or not promoter serC gene, the bacteriocin releasing factor of alkylating agent induction type and MCS.

In a preferred embodiment, the transposon plasmid that is used for screening transposon-mediated chromosomal integration bacterial strain contains:

A) be positioned at a kind of transposase gene of (outside the transposon box) outside the transposon insertion sequence, be used for the excision and the integration of transposon;

B) a kind of wild type coded sequence corresponding and the ribosome binding site and the terminator of wild type gene with the screening-gene (as serC) of bacterial isolates disappearance, but lack promoter.Preferably this sequence is located immediately at after the TN10 transposon insertion sequence of left side;

C) optional a kind of nucleotide sequence, this sequence are between the insertion sequence of the left and right sides, and a kind of release of codified promotes property nucleic acid (as BRP); And

D) a kind of multiple clone site (MCS) between the insertion sequence of the left and right sides contains single restriction site in the plasmid, is used to insert effector molecule.Preferably this MCS is located immediately at and discharges enhancement mode nucleic acid (if you are using) afterwards, and just before the TN10 insertion sequence of right side.

In another embodiment, the random integration of effector molecule on host chromosome can cause gene to interrupt, and can determine thus whether gene location is applicable to the effect insertion.

In an other embodiment, the expression vector of use is the outer plasmid of a kind of chromosome, and it is stable that this plasmid can keep under the condition that does not contain required antibiotic-screening gene, that is to say that this plasmid can self maintenance.In a non-limiting example, but the expression plasmid of self maintenance is the Salmonella virulence plasmid.

For instance, in an embodiment of the present invention, the method of keeping of plasmid screening system is the function that provides a kind of script not possess for antibacterials such as Salmonellas, and remove those on this basis and still do not possess the Salmonella of this function, thereby filter out the Salmonella that possesses this function.In an embodiment, Salmonella of the present invention is a kind of auxotrophic mutation body bacterial strain, and expression plasmid can provide the function of the biosynthetic enzyme of its shortage for this mutant.On the growth medium that lacks nutritional labeling, cultivate these cells, have only required cell can on this culture medium, carry out metabolism, the cell that just only comprises described expression plasmid can carry out metabolism, thereby can filter out the Salmonella that contains this expression plasmid.In this embodiment, highly preferred mode is that Salmonella of the present invention has inevitable demand, most preferably asd gene delection to DAP (middle meso diaminopimelic acid).DAP is a kind of composition that is present in the Peptidoglycan in the gram negative bacteria pericentral siphon, and it is necessary that this composition is that bacterial outer membrane is kept perfectly.The DAP shortage can cause the integrity of bacterial outer membrane to keep, thereby causes the antibacterial cracking.A kind of enzyme in asd (β aspartate-semialdehyde dehydrogenase) the gene codified DAP biosynthesis pathway.The gram negative bacteria that lacks the asd function can be grown adding on the culture medium of DAP.The plasmid that has the asd gene order that is connected with a kind of homology or allogeneic promoter operability, as expression plasmid of the present invention, can be screened (reference by under the condition that lacks DAP, cultivating the method that does not have the active gram negative bacteria of asd, for example, authorize Curtiss, United States Patent (USP) 5,840,483 III parts).

Other non-antibiotic type screening systems known in the art are also located within the scope of the invention.For example, what a kind of screening system employing was arranged is to contain a kind of ST and the lower antitoxic a kind of plasmid of a kind of stability, and this system can be used to screen the antibacterial of keeping this plasmid.

In another embodiment, the expression vector of use is the outer plasmid of chromosome that the enough non-antibiotic method of a kind of energy are screened, as a kind of colicine plasmid.Herein the colicine plasmid of Shi Yonging at least a kind of colicine toxin of codified and a kind of anti--colicine, the colicine toxin than anti--colicine is more stable, thereby all antibacterials of losing this colicine plasmid all can be killed because of the persistency of colicine toxin.In a preferred embodiment, the colicine toxin that uses is the big subunit of ColE3, and the anti--colicine of using is the ColE3 small subunit.

In another embodiment of the present invention, the expression vector that uses is the λ carrier, the lysogeny of more clearly saying so λ carrier.In a preferred embodiment, the bacterial host that contains the λ carrier contain in addition a kind of can be at the responsive to temperature type λ of 30 ℃ rather than 37 ℃ performance functions repressor.Therefore, this bacterial host under 30 ℃, grow and can not express when carrying out in-vivo procedures to antibacterial have toxic primary effector molecule and (or) the second order effect molecule.In case this bacterial isolates is introduced into the experimenter, then can because of normal body temperature with the deactivation of λ repressor, activate primary effector molecule and the optionally expression of second order effect molecule simultaneously.

The expression of effector molecule nucleic acid sequence encoding or fusion rotein nucleic acid sequence encoding can be regulated and control by another kind of nucleotide sequence, thereby effector molecule can be expressed in the antibacterial that this recombinant DNA molecules transforms.For example, the expression that can come the regulating effect molecule with any promoter/enhancer element known in the art.Promoter/enhancer can be homologous (being self), also can be allogenic (promptly nonself).Can be used to the effector molecule in the antibacterial, as cytokine, or the promoter of expressing fusion protein comprises, but be not limited to, prokaryotic promoter is as beta-lactamase promoter (Villa-Kamaroff et al., 1978, Proc.Natl.Acad.Sci.U.S.A.75:3727-3731) or lac promoter (DeBoer et al., 1983, Proc.Natl.Acad.Sci.U.S.A.80:21-25; ScientificAmerican, 1980,242:74-94).The present invention also comprises other promoteres, comprising, but be not limited to lacI, lacZ, T3, T7, gpt, λ P _R, λ P _L, trc, pagC, sulA, pol II (dinA), ruv, recA, uvrA, uvrB, uvrD, umuDC, lexA, cea, caa and recN (reference, for example, Schnarr et al., 1991, Biochimie73:423-431).In a preferred embodiment, the promoter of using is trc (reference, for example, Amann et al., 1988, Gene 69:301-15).

In a special embodiment, the primary effector molecule that uses is a kind of colicine of expressing under the reactive promoter regulation of SOS-, this attenuated bacteria bacterial strain can be handled with the destructive preparation of X-ray, ultraviolet, alkylating agent or other DNA, to improve the expression of colicine.The example of the reactive promoter of SOS-includes, but are not limited to, recA, sulA, umuC, dinA, ruv, uvrA, uvrB, uvrD, lexA, cea, caa, recN, or the like.

In another preferred embodiment, the activity of promoter in tumor environment strengthened; For example, the promoteres such as P1 promoter of pepT gene can be activated by the oxygen-free environment of tumor.The activation of P1 promoter depend on the FNR activating transcription factor (Strauch et al., 1985, J.Bacteriol.156:743-751).In a special embodiment, the P1 promoter of using is a kind of mutant, this promoter is compared with natural P1 promoter, can be under oxygen free condition by higher level induce, pepT200 promoter for example, this promoter is to be induced by CRP-cAMP to the reactivity of oxygen free condition, rather than FNR (Lombardo et al., 1997, J.Bacteriol.179:1909-1917).In another embodiment, use be the anaerobic inducible promoter, as the potABCD promoter.PotABCD be a kind of operon of can be under oxygen free condition expressing from the pepT Divergence (Lombardo et al., 1997, J.Bacteriol.179:1909-1917), it can the method according to this invention be used.

As selection, also can use the antibiotic inducible promoter, as the tet promoter of Tn10 transposon.In a preferred embodiment, the tet promoter of use is many bodies, as trisome.After utilizing the attenuated bacteria that is oriented to tumor of the present invention that the experimenter is handled, the tetracycline of suitable dosage is delivered medicine to the activity that this experimenter can induce this promoter.The initial tet inducible expression system of describing is to be used for pombe fission yeast (Faryar and Gatz, 1992, Current Genetics 21:345-349) eukaryotic system and mammalian cell (Langand Feingold such as, 1996, and nearest research can make its suitability expand to bacterial cell Gene 168:169-171).For example, people such as Stieger (1999, Gene 226:243-252) prove, when the Lampyridea luciferase genes with after tet promoter operability is connected, can induce by tet and obtain 80 times inducing action.The advantage of this promoter is that it can be induced under extremely low tetracycline level, this level is about 1/10th of antibiotic activity required dosage.

Be introduced into the attenuated bacteria that is oriented to tumor in case contain the plasmid of effector molecule or fusion rotein, can measure by any method pairing effect molecule known in the art or Expression of Fusion Protein, these methods comprise, but be not limited to, Determination of biological activity method, the enzyme activity algoscopy, rna blot analysis method and western blot analysis method.(with reference to Sambrook et al., 1989, Molecular Biology, A Laboratory Manual, Cold SpringHarbor Laboratory Press, Cold Spring Harbor, NY; Ausubel etal., 1995, Current Protocols in Molecular Biology, GreenPublishing, New York, NY).5.7. Combination treatment

In certain embodiments, the attenuated bacteria that is oriented to tumor can be worked in coordination with the treatment that is used for solid tumor with other known cancer therapies.In some other embodiment, express through processing one or more nucleic acid molecules the attenuated bacteria that is oriented to tumor can with the collaborative treatment that is used for solid tumor of other known cancer therapies, these one or more effector molecules of nucleic acid molecules codified and (or) fusion rotein.For instance, the attenuated bacteria that is oriented to tumor of expressing one or more nucleic acid molecules through processing can use with chemotherapeutics is collaborative, these one or more effector molecules of nucleic acid molecules codified and (or) fusion rotein.The example of chemotherapeutics comprises, but be not limited to, cisplatin, ifosfamide, taxanes such as paclitaxel and paclitaxol, I type topoisomerase enzyme inhibitor is (as CPT-11, the holder pool is for bearing, 9-AC and GG-211), gemcitabine, vinorelbine, oxaliplatin, 5-fluorouracil (5-FU), folinic acid, vinorelbine, temodal, cytochalasin B, Gramicidin D, ipecine, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicine, amycin, daunorubicin, dihydroxy anthracin diketone, dithranol, mithramycin, actinomycin D, the 1-boldenone, glucocorticoid, procaine, tetracaine, lignocaine, propranolol, and puromycin homologue and cyclophosphamide.As selection, the attenuated bacteria that is oriented to tumor of expressing one or more nucleic acid molecules through processing also can use with X-ray therapy (as gamma-rays or x ray) is collaborative, these one or more effector molecules of nucleic acid molecules codified and (or) fusion rotein.According to the type of cancer to be processed, can adopt any roentgenotherapia scheme.As non-limiting example, can handle with the x ray; In detail, can handle deep tumor, handle skin carcinoma with electron beam and normal voltage x ray with the high-energy ray (energy is higher than the ray of 1MeV) of megavolt level.In order to make tissue be exposed to ray, can also use the gamma-ray radiosiotope of emission, as the radiosiotope of radium, cobalt or other elements.

The present invention includes anticarcinogen and the sequential administration or the concomitant dosing method that are oriented to the attenuated bacteria of tumor.What the present invention includes anticarcinogen and the attenuated bacteria that is oriented to tumor has adjection or a synergistic combined method.

The present invention also comprises the combined method of the attenuated bacteria that is oriented to tumor that one or more anticarcinogen are different with one or more site of actions.No matter this combined method has synergism and still has adjection, and a kind of improvement therapy of the dual function based on these therapeutic agents can be provided.Therefore, new combination treatment of the present invention is compared with the single preparation therapy that adopts one of these two kinds of preparations, can produce higher curative effect.

The present invention also comprises a kind of anticarcinogen and is oriented to the order administration or the concomitant dosing method of the attenuated bacteria of tumor, attenuated bacteria wherein through processing can express one or more effector molecules and (or) one or more coding nucleic acid molecules of fusion rotein.What the present invention includes anticarcinogen and the attenuated bacteria that is oriented to tumor has adjection or a synergistic combined method, attenuated bacteria wherein through processing can express one or more effector molecules and (or) one or more coding nucleic acid molecules of fusion rotein.

The present invention also comprises one or more anticarcinogen and can express the combined method of the attenuated bacteria that is oriented to tumor of one or more nucleic acid molecules through processing, the effector molecule that these one or more site of actions of nucleic acid molecules codified are different and (or) fusion rotein.No matter this combined method has synergism and still has adjection, and a kind of improvement therapy of the dual function based on these therapeutic agents can be provided.Therefore, new combination treatment of the present invention is compared with the single preparation therapy that adopts one of two kinds of preparations, can produce higher curative effect.5.8. The method and composition that is used to send

The invention provides certain methods, be used for when the lower attenuated bacteria that is oriented to tumor of host's toxicity is delivered medicine to the host with one or more whole bodies can toxigenous primary effector molecule local delivery to tumor.In an embodiment, the primary effector molecule of use can be used to treat sarcoma, lymphoma, cancer or other solid tumors.In some non-limiting embodiments, the effector molecule of use is used in tumor locus and induces partial immunne response.

According to the present invention, can in certain methods, advantageously use the attenuation bacteria carrier that is oriented to tumor that contains a kind of nucleic acid molecules to suppress to suffer from the animal of solid tumor, the tumor growth that comprises human patients, or dwindle its gross tumor volume, or prevent that tumor cell from spreading in vivo, one or more primary effector molecules of nucleic acid molecules codified wherein and optional one or more second order effect molecules.

The invention provides the method that some send one or more primary effector molecules, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to the animal that needs this treatment, said composition contains a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more primary effector molecules that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability.The present invention also provides some to send the method for one or more primary effector molecules, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to the animal that needs this treatment, said composition contains a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more primary effector molecules and one or more second order effect molecules that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability.In an embodiment, the primary effector molecule that uses is TNF family member, cytotoxic peptide or polypeptide, anti-angiogenesis, tumor suppression enzyme, or its functional fragment.

The invention provides the method that some send one or more fusion rotein of the present invention, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to the animal that needs this treatment, said composition contains a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more fusion rotein of the present invention that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability.The present invention also provides some to send the method for one or more fusion rotein of the present invention and one or more effector molecules, be used for solid tumor is treated, the step of these methods comprises, a kind of Pharmaceutical composition is delivered medicine to the animal that needs this treatment, said composition contains a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more fusion rotein of the present invention and one or more effector molecules that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability.

In a preferred embodiment, the attenuated bacteria that is oriented to tumor that uses is Salmonella.In another embodiment, the attenuated bacteria that is oriented to tumor of use has a kind of enhancing delivery system.In a preferred embodiment, described animal is a mammal.In a height preferred embodiment, described animal is behaved.

The present invention also provides the attenuated bacteria that is oriented to tumor by a kind of, as Salmonella, sends one or more primary effector molecules and the optional combination delivering method of one or more second order effect molecules.The present invention also provides the combination delivering method of the different attenuated bacterias that are oriented to tumor, these antibacterials have one or more different primary effector molecules with (or) one or more different second order effect molecules.

The present invention also provides the attenuated bacteria that is oriented to tumor by a kind of, as Salmonella, sends the combination delivering method of one or more fusion rotein of the present invention.The present invention also provides the attenuated bacteria that is oriented to tumor by a kind of, as Salmonella, sends one or more fusion rotein of the present invention and the optional combination delivering method of one or more effector molecules of the present invention.The present invention also provides the combination delivering method of the different attenuated bacterias that are oriented to tumor, these antibacterials have one or more different primary effector molecules with (or) optional one or more different effector molecules.

Solid tumor comprises, but be not limited to, sarcoma, cancer and other solid tumors, comprising, but be not limited to germ cell line tumor, central nervous system's tumor, breast carcinoma, carcinoma of prostate, cervical cancer, uterus carcinoma, pulmonary carcinoma, ovarian cancer, carcinoma of testis, thyroid carcinoma, astrocytoma, glioma, pancreas film cancer, gastric cancer, hepatocarcinoma, colon cancer, melanoma, renal carcinoma, bladder cancer and mesothelioma.Preferably, described experimenter is a kind of animal, comprising, but be not limited to animals such as cattle, pig, chicken, Canis familiaris L., cat, horse, preferably mammal, most preferably people." treatment of solid tumor " used in the literary composition includes, but are not limited to, and suppresses tumor growth, suppresses tumor cell proliferation, reduces gross tumor volume, or suppress other parts (transfer) that tumor cell is diffused into health.

The invention provides a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more primary effector molecules that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability.The present invention also provides a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more primary effector molecules that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability and one or more second order effect molecules.

The invention provides a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more fusion rotein of the present invention that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability.The invention provides a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules, one or more fusion rotein of the present invention that these nucleic acid molecules codifieds are connected with one or more suitable promoter operability and one or more effector molecules.

The present invention also provides a kind of Pharmaceutical composition, and said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor.The present invention also provides a kind of Pharmaceutical composition, and said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, and this antibacterial contains one or more primary effector molecules and optional one or more second order effect molecules.These compositionss contain a kind of attenuation salmonella carrier and a kind of pharmaceutically suitable carrier that is oriented to tumor for the treatment of effective dose, and Salmonella carrier wherein contains one or more primary effector molecules and optional one or more second order effect molecules.The present invention also provides a kind of Pharmaceutical composition, and said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuation salmonella that is oriented to tumor, and this attenuation salmonella contains the fusion rotein of one or more parts and optional one or more effector molecules.These compositionss contain a kind of attenuation salmonella carrier and a kind of pharmaceutically suitable carrier that is oriented to tumor for the treatment of effective dose, and Salmonella carrier wherein contains one or more fusion rotein of the present invention and optional one or more effector molecules.

In a special embodiment, term " medicinal " is meant the administrative organization approval of federal government or state government, or American Pharmacopeia or be used for animal, more preferably is used for the people, enumerates on other generally acknowledged pharmacopeia.Term " carrier " is meant diluent, adjuvant, excipient, or is used for carrier with the therapeutic agent administration.These medicinal vehicles can be sterile liquids, and Ru Shui and oil comprise deriving from oil, animal or plant oil or synthetic oil, for example Oleum Arachidis hypogaeae semen, Oleum Glycines, mineral oil, Oleum sesami, olive oil, or the like.When Pharmaceutical composition is when being used for intravenous administration, preferred vehicle is normal saline.Can also use saline solution and water-soluble glucose and glycerite as the liquid mediums thing, particularly as injectable solution.Suitable pharmaceutical excipient comprises starch, glucose, lactose, sucrose, gelatin, Fructus Hordei Germinatus, rice, flour, Chalk, silica gel, sodium stearate, glyceryl monostearate, Talcum, sodium chloride, defatted milk powder, glycerol, propylene, glycol, water, ethanol, or the like.If desired, can also contain a spot of wetting agent or emulsifying agent in the compositions, or the pH buffer agent.These compositionss can adopt forms such as solution, suspension, emulsion, tablet, pill, capsule, powder, slow releasing preparation.Oral formulations can contain the vehicle of standard, for example mannitol of pharmaceutical grade, lactose, starch, magnesium stearate, saccharin sodium, cellulose, magnesium carbonate, or the like.Suitably medicinal vectorial example is described in " Remington ' s Pharmaceutical Sciences " of E.W.Martin to some extent.What these compositionss will contain the treatment effective dose is oriented to tumor treatment purification attenuated bacteria, contains the vehicle of suitable dosage simultaneously, thereby can adopt the form that is suitable for to patient's administration.Dosage form should be consistent with administering mode.

In a preferred embodiment, according to conventional method compositions is prepared as being suitable in the human vein Pharmaceutical composition of administration.The compositions that is used for intravenous administration normally waits the aseptic aqueous buffer solution of opening.If desired, also can comprise a kind of suspending agent and a kind of local anesthetic in the compositions, as lignocaine, to alleviate the pain of injection site.Generally speaking, each composition can provide separately, and also can mix the back provides with unit dosage form, for example is contained in the sealed containers such as the ampulla that indicates the activating agent component or sachette with freeze-dried powder or the form of not having an aqueous concentrate.When compositions is used to pour into administration, it can be formulated in the perfusion bottle that pharmaceutical grade sterilized water or normal saline are housed.When compositions is used for drug administration by injection, can provide a kind of ampulla that Injectable sterile water or normal saline are housed, so that before the administration each composition is mixed.

Can effectively treat or prevent the dosage of the Pharmaceutical composition of the present invention of solid tumor to depend on the characteristic of tumor, this dosage can be determined by standard clinical techniques.In addition, can also optionally carry out external test, to help to determine best dosage range.The definite dosage that should use in the preparation also depends on the order of severity of route of administration and cancer, and this dosage should be determined according to doctor's judgement and patient's situation.But suitable dosage range generally is about 1.0-1 * 10 ¹⁰C.f.u./kg; Optional about 1.0-1 * 10 ⁸C.f.u./kg; Optional about 1 * 10 ²-1 * 10 ⁸C.f.u./kg; Optional about 1 * 10 ⁴-1 * 10 ⁸C.f.u./kg; And optional about 1 * 10 ⁴-1 * 10 ¹⁰C.f.u./kg.Effective dose can be obtained by the dose-response curve extrapolation of testing in vitro system or animal model test macro.

There is multiple different known delivery system to can be used for Pharmaceutical composition administration of the present invention.Introducing method includes, but are not limited to, intradermal approach, intramuscular approach, intraperitoneal approach, intravenous route, subcutaneous route, intrathecal route, intranasal approach, epidural approach, and oral route.Introducing method can also be an approach (for example directly delivering medicine to tumor region) in the tumor.

Compositions of the present invention can be carried out administration by any approach easily, for example perfusion or bolus injection, or absorb (as oral mucosa, mucous membrane of rectum and intestinal mucosa etc.) by epithelial layer or mucous layer, also can with the together administration of other biological activating agent.Medication can be a whole body, also can be partial.In addition, can also Pharmaceutical composition of the present invention be introduced the central nervous system by any suitable approach, as indoor injection and intrathecal injection; Can realize intracerebral ventricle injection easily with a kind of intraventricular catheter, for example link, as the Ommaya storage with a kind of storage.Also can adopt pulmonary administration, method is for example, to use a kind of inhaler or aerosol apparatus, and prepare with a kind of aerosol.

In a special embodiment, can be with the zone of Pharmaceutical composition topical of the present invention in the needs treatment; Its implementation can be for example, but to be not limited to, in operation process, carry out regional perfusion, injection, a kind of conduit of use, or to use a kind of implant, this implant can be porous material, pore-free material or colloidal material, comprising fiber or film, as the sialastic film.In an embodiment, medication can be directly to inject at malignant tumor or tumprigenicity tissue or pre-neoplastic sex organization position (or forming position).

Contain one or more primary effector molecules and optionally the attenuated bacteria that is oriented to tumor of one or more second order effect molecules can send with a kind of controlled release system.Contain one or more fusion rotein of the present invention and optionally the attenuated bacteria that is oriented to tumor of one or more effector molecules also can send with a kind of controlled release system.In an embodiment, can use a kind of pump (with reference to Langer, Supra; Sefton, CRC Crit.Ref.Biomed.Eng.14:201 (1987); Buchwald et al., 1980, Surgery 88:507; With Saudek et al., 1989, N.Engl.J.Med.321:574).In another embodiment, can use the polymeric material (can be with reference to Medical Applications ofControlled Release, Langer and Wise (eds.), CRC Pres., BocaRaton, Florida (1974); Controlled Drug Bioavailability, DrugProduct Design and Performance, Smolen and Ball (eds.), Wiley, New York (1984); Ranger and Peppas, J.Macromol.Sci.Rev.Macromol.Chem.23:61 (1983); Can also be with reference to Levy et al., 1985, Science 228:190; During et al., 1989, Ann.Neurol.25:351; With Howard et al., 1989, J.Neurosurg.71:105).In an other embodiment, a kind of controlled release system can be placed on therapeutic goal near, be brain near, so only need to use whole-body dose a part (can reference, for example, Goodson, inMedical Applications of Controlled Release, supra, vol.2, pp.115-138 (1984)).

Other controlled release system are at Langer (1990, Science 249:1527-1533) describe to some extent in the summary, these systems all can be used for containing one or more primary effector molecules and the optionally administration of the attenuated bacteria that is oriented to tumor of one or more second order effect molecules.

The present invention also provides a kind of medicated bag or medicinal reagent box, wherein contains one or more containers, and one or more compositions of Pharmaceutical composition of the present invention are housed in the container.These containers can also optionally carry a explanation, and its form meets the regulation of the government organs of production, use or the sale of managing medicine or biological product, and administrative organization's approved that this explanation can reflect production, uses or sell delivers medicine to the mankind with it.

The present invention also provides the method for some treatment solid tumors, and the step of these methods comprises, a kind of Pharmaceutical composition of the present invention is delivered medicine to the animal that needs this treatment, and this animal is implemented at least a known other cancer therapies.In a special embodiment, be that a kind of Pharmaceutical composition of the present invention and at least a chemotherapeutics are delivered medicine to the animal that suffers from solid tumor.The example of chemotherapeutics comprises, but be not limited to, cisplatin, ifosfamide, taxanes such as paclitaxel and paclitaxol, I type topoisomerase enzyme inhibitor is (as CPT-11, the holder pool is for bearing, 9-AC and GG-211), gemcitabine, vinorelbine, oxaliplatin, 5-fluorouracil (5-FU), folinic acid, vinorelbine, temodal, cytochalasin B, Gramicidin D, ipecine, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicine, amycin, daunorubicin, dihydroxy anthracin diketone, dithranol, mithramycin, actinomycin D, the 1-boldenone, glucocorticoid, procaine, tetracaine, lignocaine, propranolol, and puromycin homologue and cyclophosphamide.

The present invention includes the sequential administration or the concomitant dosing method of anticarcinogen such as Pharmaceutical composition of the present invention and chemotherapeutics.In a special embodiment, Pharmaceutical composition of the present invention is to carry out administration (as before 2 hours, before 6 hours, before 12 hours, before 1 day, before 4 days, before 6 days, before 12 days, before 14 days, before 1 month or before the several months) before the anticarcinogen administration.In another special embodiment, Pharmaceutical composition of the present invention is to carry out administration (after as 2 hours, after 6 hours, after 12 hours, after 1 day, after 4 days, after 6 days, after 12 days, after 14 days, after 1 month or after the several months) after the anticarcinogen administration.In a special embodiment, Pharmaceutical composition of the present invention is to follow the anticarcinogen administration.The present invention includes anticarcinogen and combined method through the attenuated bacteria that is oriented to tumor of processing codified one or more nucleic acid molecules, these nucleic acid molecules codifieds one or more have adjection or synergistic effector molecule and (or) fusion rotein.

The present invention also comprises anticarcinogen and can express the combined method of the attenuated bacteria that is oriented to tumor of one or more nucleic acid molecules through processing, the effector molecule that these one or more site of actions of nucleic acid molecules codified are different and (or) fusion rotein.No matter this combined method has synergism and still has adjection, and a kind of improvement therapy of the dual function based on these therapeutic agents can be provided.Therefore, new combination treatment of the present invention is compared with the single preparation therapy that adopts one of two kinds of preparations, can produce higher curative effect.

In an embodiment, be that a kind of Pharmaceutical composition of the present invention is delivered medicine to the animal that suffers from solid tumor, and this animal handled with X-ray therapy (as gamma-rays or x ray).In a special embodiment, the invention provides a kind of method, be used for the treatment of or prevent the unmanageable tumor of X-ray therapy.Pharmaceutical composition of the present invention can carry out the radiotherapeutic administration of carrying out simultaneously.As selection, also can after Pharmaceutical composition administration of the present invention, carry out X-ray therapy, preferably Pharmaceutical composition administration after at least 1 hour, after 5 hours, after 12 hours, after 1 day, 1 week the back, carry out X-ray therapy after 1 month again, preferredly then be (as nearly after 3 months) to carry out X-ray therapy again after the several months.

Can utilize any method known in the art before Pharmaceutical composition administration of the present invention, in the administration, or implement radiotherapy after the administration.According to tumor type to be processed, any radiation treatment plan can be used.As non-limiting example, can handle with the x ray; In detail, can handle deep tumor, handle skin carcinoma with electron beam and normal voltage x ray with the high-energy ray (energy is higher than the ray of 1MeV) of megavolt level.In order to make tissue be exposed to ray, can also use the gamma-ray radiosiotope of emission, as the radiosiotope of radium, cobalt or other elements.

In addition, the present invention also provides with a kind of Pharmaceutical composition and substitutes the method that X-ray therapy is treated tumor, X-ray therapy wherein has been proved to be the patient that maybe can be proved to be able to handling and has produced too high toxicity, just can cause unacceptable or unaffordable side effect.5.9. About the treatment of Pharmaceutical composition of the present invention or the proof of prevention practicality

Before Pharmaceutical composition of the present invention is used for the mankind, preferably the therapeutic activity or the prophylactic activity of its expection are carried out testing in vitro, carry out the body build-in test then.For example, can determine whether and specific Pharmaceutical composition must be carried out administration by the testing in vitro method, these method of testings comprise cell in vitro cultivation algoscopy, this method is that patient's tissue sample is cultivated in culture medium, and make it be exposed to Pharmaceutical composition, or with other modes with the Pharmaceutical composition administration, observe the influence of said composition then to this tissue sample.

Can test the ability that Pharmaceutical composition of the present invention increases immune cell activated, method is with the Pharmaceutical composition of test or contrast contact immunocyte, and detects this Pharmaceutical composition to the bioactive adjusting of immunocyte (as improving) ability.Test composition to the assessment method of the bioactive regulating power of immunocyte can be, detect the activation of cytokine or antigenic expression, the propagation that detects immunocyte, detection signal molecule, the effector function of detection immunocyte, or detect the differentiation of immunocyte.Being used to measure these active technology is understood by those skilled in the art.For instance, can mix by the 3H-thymidine and measure and trypanosomicide orchid cell counting detects the propagation of cell.Can pass through, for example, immunoassay detects cytokine and antigenic expression, comprising, but be not limited to, competitive assay system and noncompetitive are measured system, and the technology that these systems adopt has Western blotting, the immunohistochemistry radioimmunoassay, ELISA (enzyme-linked immunosorbent assay), " interlayer " immunoassay, immunoprecipitation assay, precipitin reaction, the GDP reaction, the immunodiffusion algoscopy, agglutination assay, complement fixation assay, the immune radiating measurement method, fluorescence immunoassay, protein A immunoassay and facs analysis method.The activation of signaling molecule can be passed through, and for example, kinase assay and electrophoretic mobility analytic process (EMSAs) detect.The effector function of T cell can pass through, and for example, 51Cr discharges algoscopy and measured (reference, for example, Palladino et al., 1987, Cancer Res.47:5074-5079 and Blachere et al., 1993, J.Immunotherapy 14:352-356).

Can test Pharmaceutical composition of the present invention makes the intravital tumor of the animal that suffers from cancer form the ability that reduces.Can also test Pharmaceutical composition of the present invention and alleviate the ability of one or more symptoms relevant with solid tumor.In addition, can also test the ability that Pharmaceutical composition of the present invention prolongs the patient's who suffers from solid tumor survival period.The technology that is used for analyzing in animal body these functions of Pharmaceutical composition of the present invention is understood by those skilled in the art.

In different special embodiments, can carry out external test with the representative cell of solid tumor relevant cell type, can produce the influence of expection to such cell to determine Pharmaceutical composition of the present invention.

Before carrying out the human test, can in the appropriate animal model system, test the Pharmaceutical composition of the present invention that is used for the treatment of, comprising, but be not limited to, rat, mice, chicken, cattle, monkey, pig, Canis familiaris L., rabbit, or the like.Before human administration, can carry out the body build-in test with any animal model system known in the art.

The following example rather than limits the scope of the invention only as an illustration.6. Embodiment: express TNF-α by the attenuation salmonella that is oriented to tumor

Following embodiment illustrates, contains a kind of attenuated bacteria that is oriented to tumor of TNF family member coding nucleic acid molecule, as Salmonella, can express this TNF family member.6.1. The structure of TNF-α plasmid

The plasmid of describing in the literary composition can be used as the illustrative example of special embodiment of the present invention.Those skilled in the art removes very much, by methods known in the art can with other suitable promoteres or effector molecule replace such as the trc promoter and (or) promoter such as TNF-α code nucleic acid and (or) the effector molecule code nucleic acid.

The bacterial expression based on plasmid of effector molecule code nucleic acid adopts trc promoter and Trc99A plasmid (can buy from Pharmacia) or TrcHisB plasmid (can buy from InVitrogen).Two kinds of plasmids all are to use the NcoI site as start codon, are a multiple clone site then.6.1.1. The pCET plasmid

The bacterial expression based on plasmid of effector molecule code nucleic acid adopts two λ P _LPromoter or two λ P _RPromoter, the construction method of pCET plasmid is as follows.Shear pCE33 plasmid (Elvin et al., 1990, Gene 87:123-126) with Restriction Enzyme ClaI, the reuse mung-bean nuclease makes terminal passivation, shears with Restriction Enzyme BamHI then.Then the 1.4kb fragment that obtains is connected to the 2.1kb SspI/BamHI fragment of pUC19 (can buy from GIBCO), promptly produces the pCI plasmid.Shear the pCI plasmid with Restriction Enzyme BamHI, the reuse mung-bean nuclease makes terminal passivation, shears with Restriction Enzyme AflIII then.The 0.6kb fragment that contains little cistron and terminator that will obtain then is connected in the 3.1kb fragment of pCI, promptly obtains the pCET plasmid.PCET is the same with Trc99A or TrcHisB, as start codon, is a multiple clone site with the NcoI site then.Have any λ of comprising P in 30 ℃ of cultivations _LOr λ P _RThe antibacterial of the plasmid of promoter.6.1.2. The pTS plasmid

The pTS plasmid adopts transposon-mediated chromosomal integration method, and contains the serine prototroph screening-gene of effector molecule code nucleic acid, and the construction method of this plasmid is as follows.Shear pNK2883 plasmid (can buy) with Restriction Enzyme BamHI, and isolate the 4.8kb fragment from American type culture collection (ATCC).Utilize PCR method from Salmonella typhimurium 14028 bacterial strains (can buy), to isolate Salmonella typhimurium serC code nucleic acid from ATCC, the sequence of the forward primer that PCR uses is GAAGATCTTCCGGAGGAGGGGAAATG (SEQ ID NO:1), and the sequence of reverse primer is CGGGATCCGAGCTCGAGGGCCCGGGAAAGGATCTAAGAAGATCC (SEQ ID NO:2).Shear the PCR reactant mixture and isolate the PCR product of 1.1kb with Restriction Enzyme BglII and BamHI, this product is connected in the 4.8kb fragment of pNK2883, promptly obtain to be called as the plasmid of pTS.The cloning site that is located immediately at serC code nucleic acid 3 ' end can be used to insert the effector molecule code nucleic acid.6.1.3. PTS-TNF-α plasmid

Have a kind of plasmid (pTS-TNF-α) can make humanTNF-'s code nucleic acid of trc promoters driven carry out the chromosomal integration of pTS mediation, the construction method of this plasmid is as follows.ASD plasmid PYA272 (reference, for example, Curtiss, the United States Patent (USP) 5 of III, 840,483) replication origin by the colE1 plasmid (reference, for example, Bazaral and Helsinki, 1970, Biochem 9:399-406) after replacing, replication origin just becomes the PYA3332 plasmid.Shear the PYA3332 plasmid with Restriction Enzyme NcoI, and make terminal passivation with mung-bean nuclease.Shear the blunt ends fragment of gained then with Restriction Enzyme HindIII, and isolate the dna fragmentation of 3.3kb.Then with Restriction Enzyme NdeI shear humanTNF-'s code nucleic acid of optimizing through escherichia coli shown in Figure 1 (with reference to Pennica et al., 1984 Nature 312:724-729; And Salztman, et al., 1996, Cancer Biotherapy 11:145-153), and make terminal passivation with the T4DNA polymerase, shear with Restriction Enzyme HindIII then.The 0.5kb fragment of gained is connected in the 3.3kb fragment of PYA3332, promptly obtains Asd34TNF-α plasmid.Usefulness Restriction Enzyme BglII shearing Asd34TNF-α plasmid, and the 1.1kb fragment of the TNF-α code nucleic acid of the trc promoters driven of will encoding then is connected in the BamHI site of pTS, promptly obtains pTS-TNF-α plasmid.6.1.4. The pTS-BRP plasmid

PTS-BRP contains through transposon-mediated and be incorporated into BRP code nucleic acid in the chromosome, and contains the serine prototroph screening-gene of effector molecule code nucleic acid, and the construction method of this plasmid is as follows.Utilize the PCR method (can be from Bio101 from the pSW1 plasmid, Vista, the CA purchase) isolates the BRP code nucleic acid in, and be cloned into (can be from InVitrogen in the TOPO-TA cloned plasmids, Carlsbad, CA buys), i.e. acquisition is called as the plasmid of pBRP#5, the sequence of the forward primer that PCR uses is CCGACGCGTTGACACCTGAAAACTGGAG (SEQID NO:5), and the sequence of reverse primer is CCGACGCGTGAAAGGATCTCAAGAAGATC (SEQID NO:6).Shear the pBRP#5 plasmid with Restriction Enzyme ApaI and BamHI, and the 0.6kb fragment that contains the BRP code nucleic acid that will obtain is connected in the 5.9kbApaI/BamHI fragment of proto-pTS, promptly obtains the pTS-BRP plasmid.The cloning site of 5 ' and 3 ' end of BRP code nucleic acid can be used to insert the effector molecule code nucleic acid.6.1.5. PTS-BRPTNF-α plasmid

Have a kind of plasmid (pTS-BRPTNF-α) can make the TNF-α code nucleic acid of BRP code nucleic acid and trc promoters driven carry out the chromosomal integration of pTS mediation, the construction method of this plasmid is as follows.Shear the above-mentioned Asd34TNF-α plasmid that is used to make up pTS-TNF-α with Restriction Enzyme BglII, the 1.1kb fragment of the TNF-α code nucleic acid of the trc promoters driven of will encoding then is connected in the BamHI site of pTS-BRP, promptly obtains pTS-BRPTNF-α plasmid.6.2. The effector molecule code nucleic acid is incorporated in Salmonella host's the chromosome

System described herein adopts the Δ serC-auxotroph Salmonella bacterial strain of serine or glycine, and can rebuild the anauxotrophic plasmid of serine/glycine after being incorporated into chromosomal active transcriptional domain.But those skilled in the art understands, and the screening of chromosomal integration bacterium also can be used other selection markers, and these labellings are also located within the scope of the invention.Can reference, for example, Kleckner et al., 1991, Meth.Enzymol.204:139-180.

There is multiple method well known in the art to can be used to the pTS or the pTS-BRP plasmid that contain the effector molecule code nucleic acid are introduced serC-Salmonella bacterial strain, comprising chemical transformation and electroporation.After introducing the effector molecule code nucleic acid, in containing the growth medium of ampicillin, Salmonella was cultivated 2 hours at least, more preferably cultivated 6 hours or the longer time.Then antibacterial is placed in the culture medium that can screen the serine prototrophic bacteria.Atlas, R.M. " microbiological culture media handbook " L.C.Parks, ed.CRC Press, Boca Raton, Florida, 1993.The antibacterial that contains chromosomal integration effector molecule code nucleic acid can grow on this selection culture medium.The expression of mensuration effector molecule code nucleic acid as described below then.The expression of effector molecule code nucleic acid can be measured by any several method well known by persons skilled in the art, as the enzyme activity, biological activity, rna blot analysis, or western blot analysis.6.2.1. The TNF-α that is expressed by Salmonella sending and expressing

TNF-α code nucleic acid with the trc promoters driven as indicated above is inserted in the BamHI site of pTS-BRP, promptly obtains pTS-BRPTNF-α plasmid.The conventional method of utilizing this area is with pTS-BRPTNF-α plasmid electroporation (with reference to international monopoly WO99/13053) in the Salmonella typhimurium attenuated strain VNP20009 bacterial strain, this bacterial strain is built into the serC-deficiency, thereby its genotype is Δ msbB, Δ purI, Δ serC (Fig. 2).Although be not subjected to the restriction of principle, this plasmid integration can make the serC code nucleic acid activate after in the genome of this antibacterial, thereby produces serC ⁺Phenotype.Therefore, the antibacterial behind the electroporation is layered on the M56 agar plate of adding adenine, can filters out the antibacterial that has chromosomal integration TNF-α code nucleic acid.The further evaluation of antibacterial shows that it has lost amicillin resistance, and this expression plasmid is lost, and based on the also forfeiture thereupon of TNF-alpha expression of plasmid.

For the TNF-alpha expression to the antibacterial that is oriented to tumor detects and quantitatively, will have the Salmonella overnight incubation of chromosomal integration TNF-α code nucleic acid, get culture samples then and carry out western blot analysis and measure.A kind of representational ampicillin sensitivity serC of the special demonstration of Fig. 3 ⁺Clone's TNF-alpha expression, this clone is called as pTS-BRPTNF-α clone 2.Western blot analysis is the result show, 3.9 * 10 ⁷The pTS-BRPTNF-α of cfu clones 2 antibacterials (the 1st swimming lane) and has expressed the above TNF-α albumen (the 5th swimming lane) of 50ng, illustrates that the expression of TNF-α is higher than 10ng/10 ⁷Antibacterial.Therefore, successfully give expression to the humanTNF-by the chromosomal integration TNF-α code nucleic acid of trc promoters driven in the Salmonella.7. Embodiment: the attenuated bacteria that is oriented to tumor of expressing the OMPA fusion rotein

Pericentral siphon location after albumen and unlike signal peptide merge is all relevant with the signal peptide and the albumen that use.For example, the fusion of signal peptide and proteic aminoterminal can make this albumen be positioned the pericentral siphon chamber of antibacterial.Although be not subjected to the restriction of principle, the inventor thinks that the pericentral siphon location can promote the release of antibacterial composition (as albumen), can be released in the surrounding because this composition only need be crossed over monofilm.By contrast, the localized composition of kytoplasm inner membrance and the adventitia that need cross over antibacterial just can be released in the surrounding.In addition, some proteic pericentral siphon location is also favourable to its biological activity.

There are multiple methods known in the art to can be used for effector molecule guiding pericentral siphon of the present invention.This embodiment explanation, ompA signal peptide are merged with the aminoterminal of effect molecules such as TNF-α, TRAIL (apoptosis induction ligand relevant with TNF-α) and interleukin-2 can make these albumen be positioned pericentral siphon and processed subsequently.7.1. The processing of OMPA-TNF-alpha fusion protein

Utilize the western blot analysis method of full cell lysate to detect four kinds of different TNF-alpha expressions of cloning, these four kinds of clones can carry out expressing based on the ompA-TNF-alpha fusion protein of the trc promoters driven of plasmid in the JM109 antibacterial.The localized method of proof of pericentral siphon is that a kind of signal peptidase that the precursor fusion rotein can be located in pericentral siphon cuts into sophisticated TNF-α.After inducing with IPTG, all four kinds of clones' TNF-α crosses expression all makes TNF-α show as two migration lines (Fig. 5,4-7 swimming lane) of about 20kd, and these two lines are equivalent to form unprocessed and processing.For ease of relatively, have chromosomal integration TNF-α code nucleic acid and can express the Salmonella bacterial strain of maturation (processing) form TNF-α as positive control (Fig. 5, the 3rd swimming lane) with a kind of.In the antibacterial that does not contain TNF-α code nucleic acid, do not detect TNF-alpha expression (Fig. 5, the 2nd swimming lane).

These presentation of results, the fusion rotein (as shown in Figure 4) of humanTNF-'s albumen of mature form and escherichia coli ompA signal peptide can cause pericentral siphon location and processing when expression in escherichia coli.In addition, do not know also whether cross expressing of a kind of secretory protein can be because compacting normal secretion device to the host bacteria toxigenicity.This expression of results of the ompA-TNF-α of form processing then shows, secretes device normally and can hold high-caliber secretory protein expression.7.2. The processing of OMPA-TRAIL fusion rotein

The ability that makes the TNF family member be positioned pericentral siphon the ompA signal peptide expands to another kind of TNF family member TRAIL (apoptosis induction ligand relevant with TNF-α).In these experiments, be that the TRAIL code nucleic acid of will express the trc promoters driven of mature form people TRAIL (hTRAIL) merges (as shown in Figure 6) mutually with the coded sequence of ompA signal peptide.Two kinds of different ompA/TRAIL types of attachment have been detected altogether, NcoI site of a kind of codified, NdeI site of another kind of codified (with reference to the sequence that contains NdeI of figure 6).Fig. 7 shows two types clone's western blot analysis result.What western blot analysis adopted is a kind of anti-hTRAIL antibody, its result shows, after the ompA-TRAIL of employing NcoI connected mode crosses in antibacterial and expresses, can produce (28.2kd) of form processing and (30.2kd) hTRAIL (Fig. 7 of undressed form simultaneously, the 2-4 swimming lane), and the ompA-TRAIL that adopts the NdeI connected mode only produces the hTRAIL (Fig. 7,4-7 swimming lane) of form processing after the mistake expression in antibacterial, and this explanation NdeI connected mode can obtain more effective processing.

These presentation of results, the fusion rotein of people's trail protein of mature form and escherichia coli ompA signal peptide can cause pericentral siphon location and processing.In addition, do not know also whether cross expressing of secretory protein can be because compacting normal secretion device to the host bacteria toxigenicity.This expression of results of the ompA-TRAIL of form processing then shows, secretes device normally and can hold high-caliber secretory protein expression.7.3. The processing of OMPA (8L)-IL-2 fusion rotein

With a kind of second order effect molecule of fusion protein form expression (IL-2).Ripe (C125A) hIL-2 is merged the processing that can not cause IL-2 with the wild type ompA signal peptide that above is used for TNF-α and TRAIL.For pericentral siphon location and the processing that detects human IL-2's effector molecule, people (C125A) IL-2 of mature form is merged mutually with a kind of ompA modification signal peptide that is expressed as ompA (8L), as shown in Figure 8.This ompA modifies improving one's methods of signal peptide, with the 6-17 amino acids in the aminoacid replacement ompA signal peptide shown in Figure 8.Fig. 9 shows the testing result (the 6th and the 7th swimming lane) of its expression and processing.Each swimming lane is represented a monoclonal.The result of western blot analysis shows, uses ompA (8L) signal peptide can cause processing substantially completely (Fig. 9, the 6th and the 7th swimming lane).7.4. The processing of PHOA (8L)-IL-2 fusion rotein

Detect the pericentral siphon location and the processing of human IL-2's another kind of fusion rotein, and compare with the 7.3rd fusion rotein that saves.Express and what process detection is people (C125A) IL-2 of mature form shown in Figure 10 and the fusion rotein that phoA modifies signal peptide, this fusion rotein is expressed as phoA (8L).Fig. 9 shows the testing result of its expression and processing.Use phoA (8L) composite signal peptide can cause part processing (Fig. 9, the 4th and the 5th swimming lane), and use ompA (8L) signal peptide can cause processing more completely (Fig. 9, the 6th and the 7th swimming lane).

These results show that the location of IL-2 can provide with different signal peptides with processing.These results also illustrate, albumen is all relevant with the signal peptide and the albumen that use with the pericentral siphon location after the unlike signal peptide merges.

The result of study of these fusion rotein shows, can make second order effect developed by molecule of the present invention such as IL-2 by the method that merges with protein signal peptides such as OmpA or PhoA and be positioned the antibacterial pericentral siphon.Those of ordinary skill in the art understands, can also realize the pericentral siphon location of effector molecule with other signal peptides.Those of ordinary skill in the art also knows, can substitute the effector molecule of describing among these embodiment with other effector molecules of the present invention.8. Embodiment: Salmonella (Δ MSBB, Δ PURI) anti-of expressing mature form TNF-α Function of tumor

Following embodiment explanation, the attenuated bacteria that is oriented to tumor that contains the code nucleic acid of a kind of primary effector molecule (as a kind of TNF family member) can be delivered to mammiferous tumor with this primary effector molecule, and can cause gross tumor volume to reduce.

The ability that evaluation TNF-alpha expression improves the antitumor action of Salmonella typhimurium in the Mus colon 38 cancer models of specific period.These experiments are the 1mm of colon 38 tumors ³Tumor fragment is transplanted in the C57BL/6 mice, makes tumor growth to the about 0.3g of mean size, and this moment is with these animal random packet (n=10) and carry out following processing: 1) do not handle; 2) Salmonella typhimurium (Δ msbB, Δ purI, serC ^-) (parental strain); With 3) pTS-BRPTNF-α (above-mentioned clone 2).Each is organized mice or does not handle, or accepts 1 * 10 ⁶The single intravenous injection of the suitable bacterial strain of cfu.During from microbionation, measure the tumor size weekly.

Can express in a group of the attenuation salmonella that is oriented to tumor of TNF-α in injection, handle the back and the 2nd week promptly showed tangible tumour regression, the tumor of 6 mices of discovery degenerate fully (Figure 11) in 4 weeks after processing.In processed group not, the size of tumor increases gradually, and at parental generation Salmonella typhimurium (Δ msbB, Δ purI, serC ^-) in the bacterial strain handle a group, handle back 3-shows tumor between the 4th week part and degenerate, after this, the size of tumor increases (Figure 11) gradually.

Effect molecules such as TNF family member can be expressed and be sent to tumor to these presentation of results, the attenuation salmonella that is oriented to tumor.This Salmonella can be used for tumor treatment, and compares the degeneration that can promote tumor with the parental generation Salmonella bacterial strain of not expressing the TNF family member.

Salmonella by chromosomal integration expression of nucleic acid TNF-α can make tumor degenerate fully, and the effector molecule code nucleic acid of this explanation chromosomal integration can carry out the effective expression on the biological significance.9. Embodiment: strengthen sending of nucleic acid molecules by the antibacterial of expressing BRP

In order to prove that the plasmid that the BRP activity can promote Salmonella etc. to be oriented to the attenuated bacteria of tumor discharges, a kind of attenuation salmonella bacterial strain that is oriented to tumor is made up, make it contain the BRP that is positioned on the plasmid, and contain another kind of plasmid (pTrc99a that has the AMP labelling) as release mark.In order to measure the activity of BRP, utilize conventional method will contain BRP or the Salmonella that do not contain BRP is cultivated in culture medium.Remove any antibacterial that retains in the gained supernatant by centrifugal or filtration again, then clarifying supernatant is added in the competent cell, and carry out conversion reaction.Then these " acceptance " cells are tiled on the LBamp, with the intake of observation AMP marker plasmid.If BRP increases the quantity of AMP resistance bacterium colony, then the bacterial strain of explanation expression BRP is discharged into more plasmid in the culture medium.The results are summarized in following table 2:

Table 2

Plasmid	The average of Amp bacterium colony/transformant
Plasmid	The average of Amp bacterium colony/transformant	??pTrc99a	????125
??pTrc99a+BRP(pSW1)	????383	??pTrc99a	????125

These presentation of results, the existence of BRP increase the amp plasmid quantity that is secreted in the culture medium.Therefore, with the supernatant of the cell of expressing BRP " accepting cell " transformed and to obtain more bacterium colony.These results show that BRP has strengthened the release of second order effect molecule, comprising the release of nucleic acid plasmid.Thereby these presentation of results BRP can be used for, and plasmid discharges or DNA sends.In addition, these Salmonella bacterial strains can be expressed BRP, can DNA delivery, and can keep the replication capacity of colony.10. The expression of embodiment: BRP can not reduce the tumor of the attenuation salmonella that is oriented to tumor Guiding or tumor suppression ability

Following embodiment explanation, but the attenuated bacteria that is oriented to tumor through processing coordinate expression BRP and one or more effector molecules, and can be under the condition of the tumor targeting ability that does not suppress antibacterial accelerating effect molecule sending to tumor.

The B16 melanoma cell is subcutaneously injected into the right side aft rib of C57BL/6 mice, to obtain solid tumor models.The method of tumour transplatation is,, cleans by the flask isolated cell by trypsinization, and with 2.5 * 10 ⁶The concentration of cell/ml is suspended in the phosphate buffered saline(PBS).The 0th day, to get 0.2ml cell suspending liquid sample and inject, total amount is 5 * 10 ⁵Individual cell/Mus.After transplanting about 10 days, tumor size reaches 150-200mm ³, at random be divided into 3 group with mice this moment, and 10 every group, every group of mice accepted different processing.Matched group (curve 1 of Figure 12) is accepted 0.2ml PBS.Every mice of another group is accepted 0.2ml and contains 2 * 10 ⁶C.f.u. the attenuation salmonella bacterial strain VNP20009 that is oriented to tumor (curve 2 of Figure 12).Every mice of the 3rd group is accepted 0.2ml and contains 2 * 10 ⁶C.f.u. the attenuation salmonella bacterial strain that is oriented to tumor, this bacterial strain contains a kind of plasmid, and this plasmid contains the BRP gene, and this gene is subjected to its natural promoter regulation and control (curve 3 of Figure 12).The BRP gene is a kind of SOS inducible genes in escherichia coli, but under the condition that is not subjected to the principle restriction, the inventor thinks that this gene is a kind of part constitutive gene in Salmonella, can produce the BRP albumen of low-level or medium level, this level can further be improved by the SOS characteristic of tumor environment.Can show much at one antitumor reaction with the VNP20009 Salmonella of expressing BRP or the mice of not expressing the VNP20009 Salmonella injection of BRP, the expression of this explanation BRP does not change the survival ability or the tumor targeting ability of these Salmonellas.BRP expression and HSV-thymidine kinase (HSV-TK) are expressed the influence of the attenuation salmonella that is oriented to tumor just the opposite, the expression of HSV-TK can cause tumor suppression Disability (the Pawelek et al. of VNP20009,1997, Cancer Res.57:4537-4544).Therefore, this BRP system need not to change promptly can be used to improve primary effector molecule and (or) the second order effect molecule sends to tumor.11. Embodiment: pepT promoter expression vector

This embodiment explanation, a kind of nucleic acid molecules of reporter genes such as coding β-gal can be under the regulation and control of pepT promoter be oriented to the external and expression in vivo of the attenuated bacteria of tumor in Salmonella etc.11.1. The structure of pepT-BRP-β GAL expression plasmid

The cloning process of pepT promoter is, carries out pcr amplification to deriving from this zone that wild-type mice salmonella typhi (ATCC14028) separates bacterium colony, and the primer of use is as follows:

Forward primer: 5 '-AGT CTA GAC AAT CAG GCG AAG AAC GG-3 ' (SEQ IDNO:15)

Reverse primer: 5 ' AGC CAT GGA GTC ACC CTC ACT TTT C-3 ' (SEQ IDNO:16).

The condition of PCR comprises 1 circulation: 95 ℃ 5 minutes; 35 circulations: 95 ℃ 1 minute, 65 ℃ 1 minute, 72 ℃ 2 minutes; 1 circulation: 72 ℃ 10 minutes.(Invitrogen, Carlsbad California), promptly form PepT/PCR2.1 in the PCR2.1 cloning vehicle with the PCR product cloning.

With NcoI and XbaI digestion PepT/PCR2.1 carrier.The pepT fragment is isolated in coagulation, and is connected in β-gal Zterm carrier of using identical enzymic digestion.Zterm (the interim numbering 296495 of Genbank Bankit) is a kind of promoterless β-gal plasmid, and its production method is that β Gal open reading-frame is cloned among the pUC19.The gained plasmid is called pepT-β GAL.11.2. The activity measurement of the vivoexpression of pepT-β GAL and pepT-β GAL

The Salmonella bacterial strain YS1456 (CC14 of Figure 13 A that under anaerobic or aerobic conditions, will have pepT-β GAL; Be used for the gene assembling of bacterial strain, with reference to WO96/40238) or VNP20009 (CC16 of Figure 13 A) be cultured to OD ₆₀₀For～0.5-0.8.(1974, method J.Mol.Biol.83:447-457) is measured β-gal activity to utilize Birge and Low.The results are shown in Figure 13 A, 14-24 β-gal activity doubly that these antibacterials of this presentation of results grow and can induce under oxygen free condition.11.3. The activity measurement of the expression in vivo of pepT-β GAL and pepT-β GAL

With containing pepT-β gal expression plasmid or a kind of BRP expression plasmid (pSW1 (Vista of BIO101; California); this plasmid contains the pCloDF13BRP coded sequence; this sequence is regulated and control by its natural promoter) Salmonella YS1456 strain cell, or the Salmonella YS1456 strain cell that these two kinds of plasmids all comprise carries out intravenous injection to the mice that suffers from tumor.Inject after 5 days, with tumor and liver homogenate and isolate antibacterial, be used to prove pepT-β gal plasmid and (or) existence of BRP plasmid can not disturb the tumor targeting ability of these antibacterials.Measure the β gal activity of tumor and liver homogenate in addition, be used for determining to measure β gal activity in vivo, and whether the pepT promoter is induced in the oxygen-free environment of tumor.The results are shown in Figure 13 B, these results show the pepT promoter activity that has obtained high level in tumor environment.Compare with background level, the β gal expression in the liver does not significantly improve, and its reason may be that pepT promoter activity in the aerobic environment of liver is lower, and the liver guidance capability of (perhaps) bacteria carrier a little less than.12. Embodiment: tetracycline inducible expression system

This embodiment explanation, a kind of nucleic acid molecules of reporter genes such as coding β-gal can expressed in Salmonella etc. is oriented to the attenuated bacteria of tumor under the regulation and control of tet promoter.

Clone the tet promoter by pcr amplification from the little transposon of TN10, the primer of use is as follows:

Forward primer: 5 '-GGA TCC TTA AGA CCC ACT TTC ACA TTT AAG T-3 ' (SEQ ID NO:17)

Reverse primer: 5 '-GGT TCC ATG GTT CAC TTT TCT CTA TCA C-3 ' (SEQID NO:18).

The PCR condition is as follows: 1 circulation: 95 ℃ 5 minutes; 35 circulations: 95 ℃ 1 minute, 60 ℃ 1 minute, 72 ℃ 2 minutes; And 1 circulation: 72 ℃ 10 minutes.

Coagulation isolates～the PCR fragment of 400bp, and it is cloned into (Invitrogen) in the PCR2.1 carrier.With NcoI and BamHI digestion PCR2.1/tet promoter vector.Coagulation isolates～the tet promoter fragment of 400bp, and be connected among the promoterless β-gal carrier Zterm that uses two kinds of identical enzymic digestions.Transform with the connection mixture, and the antibacterial that transforms is layered on tetracycline/X-gal flat board.Go out positive bacterium colony according to blue color separated.The extract for preparing several positive bacterium colonies, and containing under the condition of tetracycline (1974, method J.Mol.Biol.83:447-457) is measured β-gal activity with Birgeand Low.Isolate a kind of clone, and be determined at the interior β-gal expression of a kind of concentration range of tetracycline.Measurement result is shown in Figure 14, and this presentation of results tetracycline can induce the β-gal activity of dose dependent.13. Embodiment: the attenuation salmonella that is oriented to tumor of chalone is to tumor growth in expressing Suppress

The production method of the attenuation salmonella that is oriented to tumor of chalone and this Salmonella were to the cylinder therapeutic effect of tumor in following embodiment illustrated and expresses.13.1. The structure of interior chalone expression plasmid

Utilize PCR method to amplify interior chalone from people's Placenta Hominis cDNA storehouse, the primer of use is as follows:

Forward primer: 5 '-GTG TCC ATG GGG CAC AGC CAC CGC GAC TTC CAG-3 ' (SEQ ID NO:19)

Reverse primer: 5 '-ACA CGA GCT CCT ACT TGG AGG CAG TCA TGA AGCT-3 ' (SEQ ID NO:20).

Gained PCR is called is cloned into (Invitrogen) in the PCR2.1 carrier.Above-mentioned plasmid with structure is that the template pcr amplification goes out six polyhistidyls-Nei chalone, and the primer of use is as follows:

Forward primer: 5 '-GTG TCC ATC GCT CGG CGG GCA AGT GTC GGG ACTGAC CAT CAT CAT CAT CAT CAT CAC AGC CAC CGC GAC TTC-3 ' (SEQID NO:21)

Reverse primer: 5 '-GTG CGG ATC CCT ACT TGG AGG CAG TCA TGA AGCTG-3 ' (SEQ ID NO:22).

The condition of pcr amplification comprises 1 circulation: 95 ℃ 5 minutes; 30 circulations: 95 ℃ 1 minute, 55 ℃ 1 minute, 72 ℃ 2 minutes; And 1 circulation: 72 ℃ 10 minutes.

Products therefrom is the dna fragmentation of a kind of NcoI of containing (5 ') and BamHI (3 ') restriction site, and this fragment codified aminoterminal contains the interior chalone of people of MARRASVGTDHHHHHH peptide sequence (SEQ IDNO:23).

With NcoI and BamHI digestion PCR product, the product of 550bp is isolated in coagulation, and is connected in the pTrc99A carrier with identical enzyme shearing.The product of coupled reaction is transformed into bacillus coli DH 5 alpha and is oriented in the attenuation salmonella VNP20009 bacterial strain of tumor.

Also six polyhistidyl coded sequences are cloned in the NcoI/BamHI fragment of expression vector YA3334.The replication origin of asd plasmid PYA272 (Curtiss III, United States Patent (USP) 5,840,483) by colE1 (Bazaral and Helsinki, 1970, Biochem9:399-406) replication origin is exactly the PYA3334 plasmid after replacing.Isolate the plasmid DNA that positive colony produces, and it is transformed in Salmonella 8324 bacterial strains, this bacterial strain is the VNP20009 that contains the asd sudden change.This bacterial strain is to produce according to the method that Curtiss III (United States Patent (USP) 5,840,483) describes.13.2. Carry out the vivoexpression of interior chalone by the attenuation salmonella that is oriented to tumor

The different Salmonella VNP20009 and the e.colistraindh5 that will contain pTrc99A-six polyhistidyls-Nei chalone plasmid are cultured to mid-log phase (O.D ₆₀₀～0.6-0.8), be divided into two part with each culture this moment, and portion is induced the trc promoter activity with 0.1mM IPTG, and another part does not add IPTG.Cultivated again 3 hours, and prepared bacterial extract then, and utilize anti--(Clontech, Palo Alto California) carry out western blot analysis to histidine antibody, to prove the expression of six polyhistidyls-Nei chalone.The Western blot result that Figure 15 A and 15B show has proved pTrc99A-six polyhistidyls-Nei chalone (chalone in the HexHIS-) expression among bacillus coli DH 5 alpha and the Salmonella VNP20009 respectively.The trc promoter does not show activity under the situation that lacks IPTG, but this promoter has constitutive activity in Salmonella.Six polyhistidyls-Nei chalone shows as the single band of about 25kD, and this conforms to the deduced molecular weight of this fusion rotein.

Also can express six polyhistidyls-Nei chalone fusion rotein similarly with the YA3334 plasmid that the trc promoter regulation is expressed.Can detect a kind of albumen of the deduced molecular weight with 25kDa with anti--histidine antibody, this results are shown in Figure 16.All antibacterial culturing matter samples among Figure 16 all use 0.1mM IPTG to induce 3 hours.13.3. The attenuation salmonella that is oriented to tumor of chalone is to the treatment of C38 mouse colon cancer in expressing Imitate

With 2 * 2 * 2mm ³Colon 38 tumor fragments to 9 the week ages female C57BL/6 mice carry out subcutaneous transplantation.When tumor size reaches 1000mm ³The time, take out tumor and be cut into 2 * 2 * 2mm ³Fritter.Again several times, then 2 * 2 * 2mm that obtains with the fritter continuous passage ³The fritter subcutaneous transplantation is to the right rib of female C57BL/6 mice.After transplanting about 24 days, tumor size reaches 150-200mm ³, at random be divided into 6 group with mice this moment, and 10 every group, every group of mice accepted different processing.Matched group is accepted 0.2ml PBS.Another matched group is accepted 0.2ml and is contained 1 * 10 ⁶C.f.u. the attenuation salmonella VNP20009 bacterial strain that is oriented to tumor, this bacterial strain have contrast asd plasmid, promptly above the 5.6th save the asd plasmid of describing that does not contain insertion sequence.First test group is accepted 0.2ml and is contained 1 * 10 ⁶C.f.u. a kind of VNP20009 bacterial strain, this bacterial strain can be expressed the six polyhistidyls-chalone fusion rotein on a kind of asd of being positioned at plasmid.Second test group is accepted another kind of VNP20009 bacterial strain, and this bacterial strain contains the expression construct identical with first test group, and can express BRP.

The experimental result that Figure 17 shows shows the tumor suppression effectiveness of six polyhistidyls-Nei chalone expression VNP20009 bacterial strain.Handle after 60 days, the meta tumor size of expressing the mice of VNP20009 Salmonella processing with interior chalone is about 13% of control mice, and the mice of handling than the VNP20009 Salmonella that contains empty carrier is low more than 30%.In the mice of survival, there have many mices to show as the net change value of tumor size to be very low, and the stagnation of this explanation tumor growth has a mice to show the obvious degeneration of tumor.People such as O ' Reilly (1997, find that Cell88:277-285) interior chalone can accumulate in inclusion body, so the incomplete penetration of this processing method or efficient deficiency are this interior incomplete most likely reasons of chalone delivery system.The expression of BRP can improve the efficient of this interior chalone delivery system.BRP expresses and regulated and control by its natural promoter, and this promoter is usually expressed as a kind of SOS reaction in antibacterial.Experiment shows that the expression of BRP can make the mean tumour volume of mice be reduced to about 6% of control mice mean tumour volume.In addition, with six polyhistidyls-Nei in chalone and the BRP mice of handling, have several mices to show as gross tumor volume and prolong in time and significantly reduce, these tumor size deteriorate to former gross tumor volume about 10% or lower.The effect of BRP has two aspects: the one, and itself has anti-tumor activity BRP, and the 2nd, BRP can promote the pericentral siphon composition to discharge, and promotes the release of kytoplasm composition simultaneously to a certain extent, comprising interior chalone, thereby can avoid this albumen to accumulate in inclusion body.13.4. The attenuation salmonella that is oriented to tumor of chalone is to the treatment of DLD human colon carcinoma in expressing Imitate

The DLD1 cell culture that grows to logarithmic (log) phase is carried out trypsinization, clean, in PBS, form 5 * 10 then with PBS ⁷The suspension of cell/ml.From single-cell suspension liquid, get the 0.1ml sample, wherein contain 5 * 10 ⁶Individual cell is subcutaneously injected into sample in the right rib of female nude mice (Nu/Nu-CD1 of Charles River) in 9 ages in week.Mice is divided into 3 groups at random, and 10 every group, 10-15 days or gross tumor volume reach 200-400mm after injection then ³Shi Jinhang by stages.

First group of mice is matched group, and every mice is accepted the PBS injection of 0.3ml.Second group of mice accepted 0.3ml and contains 1 * 10 ⁶C.f.u. the attenuation salmonella VNP20009 bacterial strain that is oriented to tumor, this bacterial strain have contrast asd plasmid.The 3rd group of mice accepted 0.3ml and contains 1 * 10 ⁶C.f.u. the attenuation salmonella VNP20009 bacterial strain that is oriented to tumor, this bacterial strain contains a kind of asd plasmid, and this plasmid can be expressed six polyhistidyls-Nei chalone fusion rotein and BRP.Tumor is monitored and measured weekly twice.Figure 18 is the sketch map through the gross tumor volume after these three kinds of processing, and six polyhistidyls-Nei chalone that this presentation of results is expressed by the attenuation salmonella that is oriented to tumor is to the inhibitory action of DLD1 human colon carcinoma.

The VNP20009 that has the PYA3332 empty plasmid can not obviously suppress growth of tumor.And the VNP20009 that expresses interior chalone and BRP can suppress growth of tumor.These presentation of results, the combination of interior chalone and BRP can improve the anti-tumor activity of the VNP20009 (8324 bacterial strain) that has the PYA3332 carrier.14. Embodiment: express anti-angiogenesis by the attenuation salmonella that is oriented to tumor

Following embodiment explanation is carried out method for processing to the attenuated bacteria that Salmonella etc. is oriented to tumor, and these antibacterials can be expressed anti-angiogenesis, thrombospondin AHR, PF4 and apomigren through processing.14.1. Structure contains the plasmid of thrombospondin AHR nucleic acid coding sequence

Peptide sequence TiP13.40:AYRWRLSHRPKTGFIRVVMYEG (SEQ ID NO:24) is carried out reverse design and codon optimized, be used for expressing in Salmonella, this sequence is equivalent to angiogenesis inhibitor homology region (the AHR) (reference of thrombospondin, for example, patent application C07K-14/78), the gained DNA sequence is: GCG TAC CGC TGG CGC CTG TCC CATCGC CCG AAA ACC GGC TTT ATC CGC GTG GTG ATG TAC GAA GGC (SEQID NO:25).With the synthetic this peptide of complementary oligonucleotide (Oligo13:40-1 and Oligo13:40-2).Add one section OMPA processing district coded sequence and a kind of SpeI restriction site at 5 ' end.Add termination codon and BamHI restriction site at 3 ' end.With two kinds of oligonucleotide annealing, to produce double chain DNA fragment.Shear this dna fragmentation with SpeI/BamHI, be connected with the pTrc801IL2 carrier that SpeI/BamHI shears then, promptly produce and contain the pTrc801-13.40 plasmid that total length OmpA modifies targeting sequencing.Can produce total length 13.40 thrombospondin peptides after this sequence is processed.

Oligo?13.40-1：

5’gtgt gtggcgcaggcgGCGTACCGCTGGCGCCTGTCCCATCGCCCGAAAACC

GGCTTTATCCGCGTGGTGATGTACGAAGGCTAA gcgc?3’(SEQ?ID?NO：26)

Oligo?13.40-2：

5’gcgc TTAGCCTTCGTACATCACCACGCGGATAAAGCCGGTTTTCGGGC

GATGGGACAGGCGCCAGCGGTACGC cgcctgcgccac

acac?3’(SEQ?ID?NO：27)

(italics is a restriction site, underlined recognition site for OmpA processing)

14.2. Structure contains the matter of the nucleotide sequence of coding PF4 peptide (47-70) Grain

To containing PF4 (PF-4; Reference, for example, Maione et al., 1990, Science 247:77-79 and Jouan et al., 1999, Blood 94:984-993) C-to hold the peptide of 47-70 amino acids residue to carry out codon optimized, be used for expressing in Salmonella.This peptide, as follows, to contain a kind of PF-4 of making and the CFU-GM CFU-GM is had suppress active DLQ motif, and contain a kind of basic amino acid bunch, it is a kind of main heparin land.

PF4:

(SEQID NO:28)

Signal peptide=underlined boldface type

The main heparin of Lys61,62,65,66=land (boldface type)

DLQ (7-9,54-56)=to the inhibition activity (boldface type) of CFU-GM CFU-GM

With the synthetic this peptide of complementary oligonucleotide (Oligo PF4-1 and Oligo PF4-2).Add one section OmpA processing district coded sequence and a kind of SpeI restriction site at 5 ' end.Add termination codon and BamHI restriction site at 3 ' end.With two kinds of oligonucleotide annealing, to produce double chain DNA fragment.The pTrc801 carrier of this dna fragmentation after the restrictive diges-tion with SpeI/BamHI digestion is connected, promptly produces the pTrc801-PF4 plasmid.Can produce total length PF-4 (47-70) peptide after this sequence is processed.

Oligo?PF4-1

5’cttc

gtggcgcaggcgAACGGCCGCAAAATCTGCCTGGACCTGCAGGCGCCGCT

GTACAAAAAAATCATCAAAAAACTGCTGGAAAGCTAA gcg3’(SEQ?ID

NO：29)

Oligo?PF4-2

5′

TTAGCTTTCCAGCAGTTTTTTGATGATTTTTTTGTACAGCGGCGCCTG

CAGGTCCAGGCAGATTTTGCGGCCGTTcg cctgcgccac

gtgaag3’(SEQ?ID?NO：30)

(italics is a restriction site, and the underlined OmpA of being processes recognition site) 14.3. Structure contains the plasmid of the nucleotide sequence of the apomigren that encodes

Angiogenesis inhibitor apomigren peptide (IYSFDGRDIMTDPSWPQKVIWHGSSPHGVRLVDNYCEAWRTADTAVTGLASPLSTG KILDQKAYSCANRLIVLCIENSFMTDARK (SEQ ID NO:31); Reference, for example, international monopoly WO99/29856) be equivalent to the C-end of restin, it is a kind of proteolytic fragments of collagen protein XV.Design oligonucleotides (Oligo Apom5F and Oligo Apom6F) is used for from this dna fragmentation of people cDNA amplification.Add one section OmpA processing district coded sequence and a kind of SpeI restriction site at 5 ' end.Add termination codon and BamHI restriction site at 3 ' end.Oligo?Apom5F：5′-ggcttc gtggcgcaggcgATATACTCCTTTGATGGTCG-3′(SEQID?NO：32)Oligo?Apom6R：5′-cgc TTACTTCCTAGCGTCTGTCATGAAACTG-3′(SEQ?IDNO：33)

With Placenta Hominis cDNA is template obtains to have correct size with PCR method a kind of fragment.Shear this PCR product with SpeI/BamHI, be connected with the pTrc801 carrier that contains OmpA modification signal sequence of SpeI/BamHI digestion then, promptly produce the pTrc801-Apom plasmid.Can produce the Apomigren peptide after this sequence is processed.14.4. Anti-angiogenic peptides inhibition of endothelial cell proliferation by the Salmonella generation

With chalone, pTrc801-PF4 and pTrc801-13.40 plasmid electroporation in the pTrcOmpA-in the attenuation salmonella VNP20009 bacterial strain that is oriented to tumor.Filter out the Salmonella bacterial strain of expressing chalone, pTrc801-PF4 and pTrc801-13.40 in the pTrcOmpA-, and press Feldman et al., 2000, Cancer Res.60:1503-1506 and Blezinger et al., 1999, its antiproliferative activity of the described mensuration of Nature Biotech.17:343-348.The single bacterium colony culture of 5ml was cultivated 4 hours.Cell precipitation is resuspended in the HUVEC culture medium that contains the 100mg/ml gentamycin of 1/20 volume, and carries out continuously freezing/melt circulation 3 times, promptly obtain cell lysate.Centrifugal and with the filtration sterilization of 0.2mm syringe filter, so that the lysate clarification.With 10,25 or the 50ml lysate add in 96 orifice plates that contain people's venous endothelial cell (HUVECs) and 100ml minimal medium, 2%FCS and 10ng/ml FGF.The Salmonella that contains the pTrc empty plasmid is adopted in contrast.With plate insulation 72 hours, and with the MST algoscopy (Mosman et al., 1983, J.Immunol.Methods65:55-63) breed measurement.

As if the PRELIMINARY RESULTS that shows among Figure 19 and 20 shows that PF4 peptide (PF4-2), thrombospondin peptide 13.40 (13.40-3) and the interior chalone that Salmonella is expressed has the antiproliferative activity of 40-60%.15. Embodiment: express the bacteriocin family member by the attenuation salmonella that is oriented to tumor

This embodiment illustrates, contains a kind of attenuated bacteria that is oriented to tumor of bacteriocin family member code nucleic acid, as Salmonella, can express this bacteriocin family member.15.1. The structure of COLE3 plasmid

The plasmid of describing in the literary composition can be used as the illustrative example of special embodiment of the present invention.Those skilled in the art removes very much, by methods known in the art can with other suitable promoteres or effector molecule replace such as the trc promoter and (or) promoter such as bacteriocin code nucleic acid and (or) the effector molecule code nucleic acid.15.1.1. PE3.shuttle-1 intermediate carrier plasmid

PE3.shuttle-1 is a kind of intermediate carrier, can be used for being created in the ColE3-CA38 plasmid vector with the segmental box of lacZ with clone/screening effect containing multiple clone site.For ease of BRP is cloned among the E3, at first BRP is cloned on a kind of middle shuttle vector (Figure 21).This carrier contains a kind of lacZ fragment, is used on the lactose from chromosome lacZ to contain screening and cloning the bacterial isolates of sudden change.Then the BRP fragment is cloned in the SmaI site of E3 plasmid (Figure 22) as containing the complementary segmental a kind of box of lacZ α.This step can be screened insertion sequence (being Lac+) by the lacZ fragment.Although natural E3 plasmid does not contain antibiotic-screening labelling (Figure 23), can use dizzy algoscopy (K.G.Hardy, " plasmid practical approach ", 1987, the Pugsley among the ed., A.P.and Oudega, B. " research method of colicine and plasmid thereof "; Gilson, L.et al.EMBO are J.9:3875-3884)) situation that exists of plasmid is screened.This shuttle vector helps BRP is cloned on the E3 plasmid, and can be not always the case with the DNA that E3 or E3/BRP are connected to any.The E3/BRP plasmid that will newly produce then is transformed among the 41.2.9, and carries out active testing.The dizzy PRELIMINARY RESULTS of measuring that forms illustrates that the BRP on the plasmid can not disturb the E3 of this bacterial strain to produce.In order to determine whether 41.2.9E3/BRP has higher activity than 41.2.9E3, the deadly unit quantity of E3 that each bacterial strain produces is measured (Figure 24).41.2.9E3/BRP the deadly unit quantity that produces is higher by 100% than 41.2.9E3, this illustrates that this bacterial strain has the activity higher than 41.2.9E3.15.1.2. Be used to measure active dizzy " puncture " algoscopy of E3

(SK522) is cultured to OD with the responsive type test strain ₆₀₀Be 0.8.In the LB soft agar of (～55 ℃) of 3ml preheating, add 100 μ l test strain (being used for 100 * 15mm plate), and be poured on fast on the LB agar plate.The flat board gentleness is vibrated so that covering uniform spreading on flat board makes agar solidify then 10-15 minute.Be used for the escherichia coli or the Salmonella bacterial strain of E3 determination of activity with the toothpick picking, and " puncture " is in agar.In 37 ℃ agar plate is inverted overnight incubation then.Second day, dizzy or clear zone can appear around the E3 puncture position, and this is because excretory colicine E3 has killed the responsive type antibacterial.Can also make bacterium colony of in the multiple SOS-inducers such as alkylating agent (as mitomycin), ultraviolet or X-ray any and further induce, to improve output or the secretory volume of E3.

Figure 25 shows once the dizzy result who measures.Have in a kind of culture dish of responsive type bacterial strain lawn in growth, when a kind of bacterial isolates was secreted colicine, excretory colicine can and kill the antibacterial that comprises in the lawn to external diffusion, promptly formed a clear zone or dizzy after these antibacterial cracking.Dizzy size is relevant with the secretory volume of colicine.Figure 25 shows the measurement result of multiple bacterial strain.Around the bacterial strain that does not contain the colE3-CA38 plasmid, do not observe dizzy.These Salmonella bacterial strains can produce colicine under not inductive situation.It can also be seen that in addition pass through dissimilar induce back (being alkylating agent, ultraviolet, the X-ray), all dizzy sizes all are dose dependent ground to be increased.15.1.3. The overlay measurement method that is used for selectivity E3 clone

The transformant of different dilution factors (the highest 1: 10,000) is layered on the LB, cultivated 2 hours for 37 ℃.Prepare the responsive type test strain by the description of measuring part of above swooning then, and it is covered on the soft agar.Flat board was solidified 10 minutes, be inverted overnight incubation in 37 ℃ then.Promptly occurred little clear zone (be similar to and have a liking for bacterial plaque) in second day, (or a plurality of) petite is arranged in the centre in clear zone.15.1.4 " plaque " or dizzy purification algoscopy

Isolate the petite at the center, clear zone that is positioned at above-mentioned covering agar then with aseptic pasteur pipet.When in one is swooned, not having visible bacterium colony or a plurality of bacterium colony is arranged, can choose whole dizzy with aseptic pasteur pipet.The bacterium colony that to choose or dizzy transferring among the 500 μ l LB.Carry out dilution (the highest 1: 10,000) in various degree, and be layered on again on the LB agar, cultivated 2 hours in 37 ℃ then.Above-mentioned responsive type test bacterium covers reuse.Second day, swooning all should appear in all or nearly all periphery of bacterial colonies.16. Embodiment: injection E3 in the body, and the plasmid of measuring in the Salmonella retains percentage rate

Following embodiment explanation, the colE3-CA38 plasmid can remain in the live body Salmonella.

What this research was used is tumor homogenate and the liver homogenate of two mices of 41.29 (or 41.2.9E3-CA38) injection after 30 days.In the following description, L=liver, T=tumor.All four kinds of homogenates are paved plate, and to produce CFU, picking colony also carries out the msbB pcr analysis and the colicine determination of yield.With the almost purified culture of four kinds of homogenates acquisitions with the similar bacterium colony of 41.2.9.Respectively choose 5 bacterium colonies and be used for colicine and pcr analysis.Produce colicine colony and do not produce colicine colony owing in the flat board of 41.2.9E3 liver homogenate thing, as if be mixed with, be used for further analysis so from 41.2.9E3T flat board and L flat board, choose 30 bacterium colonies again.According to these results, 100 bacterium colonies of picking the dull and stereotyped and liver flat board from the tumor of 41.2.9E3 are used for colicine output and msbB PCR mensuration again.Calculate the distribution of plasmid and retain rate by synthetic data.

Plasmid retains percentile measurement result and is shown in following table 3 in interior injection of E3 body and the Salmonella.

Table 3

Tissue	?CFU/ml	Tissue weight	?CFU/ml	The colicine number positive	Positive percentage among the msbB PCR	Plasmid retains percentage rate
Tissue	?CFU/ml	Tissue weight	?CFU/ml	The colicine number positive	Positive percentage among the msbB PCR	Plasmid retains percentage rate	?41.29L	?1.07E+03	?1.33	?4.02E+03	?0/5	?100％	n/a
?41.29T	?1.26e+07	?0.26	?2.42E+08	?0/5	?100％	n/a	?41.29L	?1.07E+03	?1.33	?4.02E+03	?0/5	?100％	n/a
?41.29T	?1.26e+07	?0.26	?2.42E+08	?0/5	?100％	n/a	?41.29E3L	?1.15E+04	?2.34	?2.46E+04	?87/135	?100％	64.44
?41.29E3T	?1.09e+06	?0.35	?1.56E+07	?134/135	?100％	99.26	?41.29E3L	?1.15E+04	?2.34	?2.46E+04	?87/135	?100％	64.44

In order to play a role in vivo, and other genes are carried into intravital tumor locus, the colE3 plasmid must retain in vivo effectively.This result of experiment is wondrous and very useful because the target of effector agent is a tumor, thereby to liver itself to influence meeting lower.17. Embodiment: the tumor orientation of different 41.2.9. bacterial strains in M27 lung tumor model

Following embodiment can illustrate the tumor targeting ability of 41.2.9colE3,41.2.9colE3 BRP and 41.2.9colE3 BRP-m (BRP of modification) Salmonella bacterial strain.

The Salmonella bacterial strain that following table 4 is enumerated is expelled in the animal that suffers from the M27 lung tumor, and at the 7th day with these sacrifice of animal.Next day, measure the organ weight and calculate cfu/g.With tumor and liver homogenate and be layered on the msbB, to measure colony forming unit (c.f.u.).In the the the 1st, the 2nd, the 4th and the 6th group, the bacterial strain that is accumulated in the tumor all is about 4 * 10 ⁸Cfu/g, and the aggregate amount in liver has nothing in common with each other, scope is 6 * 10 ⁴-4 * 10 ⁶Cfu/g.Each average cfu/g that organizes data is summarized in table 4.All bacterial strains all show good tumor aggregation and (are higher than 10 ⁸Cfu/g organizes), and accumulative ratio all is positive in tumor and liver.The ratio that is obtained by BRP colE3 is the highest, but not necessarily all available bacterial strains are all high than other.E3 and the E3BRP bacterial strain gathering level in tumor is calculated than higher, and the ratio that accumulates in tumor and liver is 100-200: 1.

Table 4

Group	Bacterial strain	Tumor (T) liver (L)	The cfu/g tissue	Ratio (tumor: liver)
Group	Bacterial strain	Tumor (T) liver (L)	The cfu/g tissue	Ratio (tumor: liver)	????1	????41.2.9/E3	????T	?5.1±1.1×10 ⁸	????131∶1
????1	????41.2.9/E3	????L	?3.9±3.6×10 ⁶		????1	????41.2.9/E3	????T	?5.1±1.1×10 ⁸	????131∶1
????1	????41.2.9/E3	????L	?3.9±3.6×10 ⁶		????2	????41.2.9/E3BRP	????T	?4.6±2.7×10 ⁸	????209∶1
????2	????41.2.9/E3BRP	????L	?2.2±1.3×10 ⁶		????2	????41.2.9/E3BRP	????T	?4.6±2.7×10 ⁸	????209∶1
????2	????41.2.9/E3BRP	????L	?2.2±1.3×10 ⁶		????6 ¹	????41.2.9/E3BRP _m	????T	?3.5±0.15×10 ⁸	????90∶1
????6 ¹	????41.2.9/E3BRP _m	????L	?3.9±3.6×10 ⁶		????6 ¹	????41.2.9/E3BRP _m	????T	?3.5±0.15×10 ⁸	????90∶1

BRP _mBe meant a kind of modification BRP that contains point mutation the 96th (G is mutated into A, causes glycine to become arginine) and the 114th (T sports A, causes serine to become threonine).BRP _mMutant no longer causes accurate cracking, but still can make antibacterial secretory protein (van derVal, F., Koningstein, G., Ten Hagen, C.M., Oudega, B.andLuirink, J. (1998) is optimized the albumen release that bacteriocin discharges albumen (BRP) mediation by escherichia coli: the random mutagenesis that derives from the BRP gene of pCloDF13 makes lethal and accurate cracking and albumen discharge uncoupling.Applied?and?EnvironmentalMicrobiology?vol.64?pp?392-398)。18. Embodiment: 41.2.9/COLE3 is to the curative effect of C38 mouse colon cancer

Following embodiment illustrates the inhibition ability of 41.2.9/ColE3 to the growth of C38 mouse colon cancer.

With colon 38 tumor fragment (2 * 2 * 2mm ³) be transplanted to the subcutaneous of C57BL/6 mice (female, 9 week ages).When tumor size reaches 1,000mm ³The time, under aseptic condition, from mice, take out the tumor and (about 2 * 2 * 2mm that is cut into small pieces ³/ piece), said process is repeated 5 times.With the tumour transplatation pin fritter is transplanted to the subcutaneous of the right rib of mice, this time was designated as tumour transplatation the 0th day.

When gross tumor volume reaches 150-200mm ³The time, with Salmonella mice is carried out administration at random, this time was designated as the Salmonella administration the 0th day.41.2.9 and 41.2.9/ColE3 with freezing preservation under the room temperature melt, and being diluted to final concentration with PBS respectively is 7.5 * 10 ⁶Cfu/ml.In the time of the 0th day, according to specifying group 0.2ml bacterial suspension sample (1.5 * 10 ⁶The CFU/ Mus) mice is carried out intravenous administration.Bacterial suspension is diluted to 1 * 10 ³CFU is layered on dull and stereotyped going up and incubated overnight then, to determine the bacterial population of administration.Weekly tumor is carried out twice measurement, finish up to experiment.Every group (ColE3) dissects 3 tumors and handles, and retains situation to determine cfu and tumor.Group:

		Mice
		Mice	????1.	Do not handle contrast	????8
????2.	????41.2.9(1.5×10 ⁶/ Mus)	????8	????1.	Do not handle contrast	????8
????2.	????41.2.9(1.5×10 ⁶/ Mus)	????8	????3.	????41.2.9/ColE3(1.5×10 ⁶/ Mus)	????8

41.2.9/ColE3 the exercising result to the C38 mouse colon cancer is shown in Figure 26.These data declarations, the mice of intravenous injection VNP20009 (41.2.9) can significantly suppress the growth of C38 mouse colon cancer.In addition, the mice of handling with the VNP20009 that contains the ColE3 plasmid can show tumour regression (little when promptly testing the tumor ratio beginning when finishing).19. Embodiment: VNP20009/COLE3 lives to the antitumor of the DLD1 human colon carcinoma in the nude mice The property

Following embodiment explanation, mutant salmonella body VNP20009/ColE3 (41.2.9/ColE3) compares the ability with higher inhibition DLD1 human colon carcinoma growth with mutant salmonella body 41.2.9.

Take out the DLD1 cell grow to logarithmic (log) phase by trypsinization, clean with PBS, and resuspended in PBS be 5 * 10 ⁷Cell/ml.In the time of the 0th day, with single-cell suspension liquid (0.1ml) be expelled to nude mice (female Nu/Nu-CD1,9 the week ages; Charles River) under the right ribbed hide (5 * 10 ⁶Cell/Mus).After the about 10-15 of tumour transplatation days, when gross tumor volume reaches 300-400mm ³The time, mice is carried out random packet also by stages with 10 every group.Needed to calculate the CFU of mutant salmonella body 41.2.9 and 41.2.9/ColE3 in 1 day in the past.(41.2.9 and 41.2.9/ColE3) is diluted to 1 * 10 with antibacterial ⁷CFU/ml.When specified natural law, with 0.2ml bacterial suspension sample (2 * 10 ⁶The CFU/ Mus) mice is carried out intravenous injection.Bacterial suspension is diluted to 1 * 10 ³CFU, each solution get 100 μ l and are layered on the msbB flat board and incubated overnight.Second day to bacterial colony count.Weekly tumor is carried out twice measurement.Group:

		Mice
		Mice	????1.	Do not handle contrast (PBS)	????10
????2.	????41.2.9(2×10 ⁶/ Mus)	????10	????1.	Do not handle contrast (PBS)	????10
????2.	????41.2.9(2×10 ⁶/ Mus)	????10	????3.	????41.2.9/ColE3(2×10 ⁶/ Mus)	????10

41.2.9/ColE3 the anti-tumor activity to DLD1 human colon carcinoma in the nude mice the results are shown in Figure 27.The 41.2.9 bacterial strain that contains colicine E3 can show the activity higher than 41.2.9 bacterial strain.20. Embodiment: 41.2.9/COLE3 is to the melanomatous treatment of B16 Mus in the C57BL/6 mice Imitate

Following embodiment illustrates the inhibition ability of mutant salmonella body 41.2.9/ColE3 to the growth of B16-F10 melanoma.

Take out the B16-F10 cell grow to logarithmic (log) phase by trypsinization, clean with PBS, and resuspended in PBS be 5 * 10 ⁶Cell/ml.In the time of the 0th day, single-cell suspension liquid (0.1ml) is expelled under the right ribbed hide of C57BL/6 mice (female, 9 week ages) (5 * 10 ⁵Cell/Mus).The 9th day, when gross tumor volume reaches 150-200mm ³The time, with the mice random packet, 10 every group.Salmonella clone 41.2.9 and 41.2.9/ColE3 with freezing preservation under the room temperature melt, and being diluted to final concentration with PBS respectively is 7.5 * 10 ⁶Cfu/ml.In the time of the 9th day, according to specifying group 0.2ml bacterial suspension sample (1.5 * 10 ⁶The CFU/ Mus) mice is carried out intravenous administration.Bacterial suspension is diluted to 1 * 10 ³CFU is layered on the msbB flat board and incubated overnight then, to determine the antibacterial cfu number of administration.Weekly tumor is carried out twice measurement, finish up to experiment.Group:

		Mice
		Mice	????1.	Do not handle contrast	????10
????3.	????41.2.9(1.5×10 ⁶/ Mus)	????10	????1.	Do not handle contrast	????10
????3.	????41.2.9(1.5×10 ⁶/ Mus)	????10	????5.	????41.2.9/ColE3(1.5×10 ⁶/ Mus)	????10

41.2.9/ColE3 the melanomatous exercising result of B16 Mus in the mice is shown in Figure 28.These data declarations, the mice of intravenous injection 41.2.9 (41.2.9) can significantly suppress the melanomatous growth of B16 Mus.In addition, compare with the mice of only handling with 41.2.9 with the mice that 41.2.9/ColE3 handles, time point (before 37 days) shows obviously reducing of tumor size in early days.This discovery is very important, and is because tumor size is more little, just responsive more to other therapies (for example radiation such as chemotherapeutics and X-ray).21. Embodiment: with the antitumor action of the bonded 41.2.9/E3 of BRP

Following embodiment explanation, BRP and the E3 coexpression in mutant salmonella body 41.2.9 can improve the antitumor action of this mutant.

BRP and the E3 coexpression in mutant salmonella body 41.2.9 can improve this antibacterial in external E3 secretory volume.If BRP can improve Salmonella E3 secretory volume in vivo, can conclude that then the increase of extracellular E3 makes it be easier to contact tumor cell, and improve cytotoxicity thus these cells.In this experiment, test 4 treated animals (10 every group) altogether:

Group number	Processing method
Group number	Processing method	????1	Contrast (not handling)
????2	????41.2.9	????1	Contrast (not handling)
????2	????41.2.9	????3	????41.2.9/E3
????4	????41.2.9/E3/BRP	????3	????41.2.9/E3

The model that this experiment is used is people's pulmonary carcinoma HTB177 system.In the time of the 1st day, the flank of cell being transplanted to mice is subcutaneous.In the time of the 14th day, when tumor reaches about 500mm ³, with 1 * 10 ⁶The described bacterial strain of table of going up of cfu carries out intravenous injection to animal, the 1st group of injecting normal saline then.Measure gross tumor volume weekly, up to the 24th day.The explanation of table 5 result displayed although 41.2.9 itself can suppress tumor growth (suppressing 40%), improves (63%) with making antitumor effectiveness after the E3 combination.And in this model, use the bacterial strain contain E3 and BRP can further improve antitumor render a service (with do not handle contrast compare can suppress 67%), this inhibiting enhancing is time point especially obviously (table 5) in early days.

Table 5: with do not handle the tumor growth compared of contrast and suppress percentage rate

Bacterial strain	The 17th day	The 20th day	The 24th day
Bacterial strain	The 17th day	The 20th day	The 24th day	????41.2.9	????50	????38	????40
????41.2.9/E3	????63	????58	????63	????41.2.9	????50	????38	????40
????41.2.9/E3	????63	????58	????63	????41.2.9/E3/BRP	????97	????82	????67

Conclusion is, compares with only handling with 41.2.9/E3 with the contrast of not handling, and handles with the Salmonella that contains cytotoxicity colicine E3 and strengthen delivery system BRP and can improve antitumor and render a service.22. Embodiment: the Salmonella that contains colicine E3 combines with the treatment of X line

Following embodiment explanation and is only compared with the processing of X-line, can obviously prolong the time-to-live of mice with 41.2.9 and 2 X-line combined treatment.

Program is as follows: the 0th day, utilize B16F10 melanoma administration (5 * 10 ⁵Cell/Mus) method is subcutaneous with the right abdomen in tumour transplatation to 100 a C57B6 female mice (5-7 age in week).The 8th day, injection contained the Salmonella 41.2.9 of colicine E3, and carried out the x-line at the 12nd and the 26th day and handle.

Table 6 shows with containing the Salmonella of colicine E3 and the result of x-ray combined treatment.

Table 6

Type	n＝()	Grow to the natural law of 1g	On average	?T/C
Type	n＝()	Grow to the natural law of 1g	On average	?T/C	The false 15Gy that handles	(6)	12，12，18，18，18， 21	?17	?1.0
J 15Gy x ray 12dpt, 26dpt	(9)	14，14，18，21，25， 35，35，67，67	?33	?1.9	The false 15Gy that handles	(6)	12，12，18，18，18， 21	?17	?1.0
J 15Gy x ray 12dpt, 26dpt	(9)	14，14，18，21，25， 35，35，67，67	?33	?1.9	K 41.2.9+15Gy x ray 12dpt, 26dpt returns #1,2	(9)	21，28，35，35，56， 60，60，60，67	?47	?2.8
L 41.2.9/E3+15Gy x ray 12dpt, 26dpt returns d32	(9)	28，39，53，56，56， 60，67，74，78	?57	?3.3	K 41.2.9+15Gy x ray 12dpt, 26dpt returns #1,2	(9)	21，28，35，35，56， 60，60，60，67	?47	?2.8

These data declarations and are only compared with the processing of X-line, can obviously prolong the time-to-live of mice with 41.2.9 and 2 X-line combined treatment.Compare with 2 X-ray combined treatment with 41.2.9, handle and further to prolong the time-to-live of mice with E3.23. Embodiment: by the bacterial expression cytotoxicity necrosin that is oriented to tumor

Following embodiment explanation, the antibacterial that is oriented to tumor can be expressed Bacillus coli cells toxicity necrosin 1 (CNF1).

The cytotoxicity necrosin includes, but are not limited to, Bacillus coli cells toxicity necrosin 1 (CNF1; Falbo et al., 1993, Infect.Immun.61:4904-4914), Fei Shi vibrio CNF2 (Lin et al., 1998, Biochem.Biophys.Res.Comm.250:462-465) and Bacillus coli cells toxicity necrosin 2 (CNF2; Sugai et al., 1999, Infect.Immun.67:6550-6557).CNF family also comprises Pasteurella multocida toxin (PMT), and the N-end parts of this toxin and CNF2 has 27% residue identical, and have 80% conserved residues (Oswald et al., 1994, Proc.Acad.Sci.USA91:3814-3818).

Utilize standard pcr to clone CNF1 from escherichia coli J96 (ATCC 700336), the primer of use is (forward) 5 '-GTGTCATGAAAATGGGTAACCAATGGCAAC-3 ' (SEQID NO:35) and (oppositely) 5 '-CACAGA GCTCGCGCTAACAAAACAGCACAAGGGAG-3 ' (SEQ ID NO:36).The product that obtains is about 3100bp, with NcoI and the SacI site of this product cloning to the pTrc99a that is used for protein expression, and carries out dna sequencing with escherichia coli as the dna clone host.Dna sequencing is to carry out with standard method at Yale University KeckBiotechnology laboratory.The result of dna sequencing proves that this PCR clone product is the CNF1 that contains 6 secondary variances in 3065 base pairs.

With CNF1 plasmid electroporation (international monopoly WO99/13053) in e. coli dna cloning host DH5 α and the Salmonella YS1646 bacterial strain.Utilize LDH algoscopy (Promega, Madison, WI, Cytotox96 ) the detection e. coli dna cloning host of standard and the CNF1 in the Salmonella YS1649 bacterial strain to express.Figure 29 shows that the existence that contains the CNF plasmid can make cytotoxicity strengthen.Measurement result afterwards shows, has other known features that the Salmonella that contains the CNF plasmid can also show CNF1, as the multinucleation effect (Rycke etal., 1990, J.Clin.Microbiol.28:694-699).Utilize optical microscope observation to be exposed to the nucleus of the Hela cell of CNF1.The result of Figure 30 shows that multinucleation and cell that the Salmonella that contains CNF1 can cause expecting increase with removing.24. Embodiment: by the bacterial expression Vero cytotoxin that is oriented to tumor

Following embodiment explanation, the antibacterial that is oriented to tumor of expressing Vero cytotoxin AB through processing can produce has Cytotoxic Vero cytotoxin AB.

Vero cytotoxin (having another name called HSC10 toxin, Shiga toxin, shiga-like toxin, shiga toxin).This toxin separates from the escherichia coli HSC10 bacterial strain that can produce colicine, thinks that originally it is colicine (Farkas-Himsley et al., 1995, Proc.Natl.Acad.Sci.92 (15): 6996-7000).Just find that a long time ago this toxin has anti-tumor activity,, but only find that the purification goods have this anti-tumor activity especially to the ovarian cancer and the cerebral tumor, rather than complete antibacterial alive.

Utilization clones the Vero cytotoxin based on the primer of delivering sequence from escherichia coli HSC10 (ATCC 55227), and is proved by carrying out dna sequencing at Yale Keck biotechnology center with the standard DNA sequencing technologies.BRP gene that is subjected to the regulation and control of tetracycline inducible promoter and the polycistron that contains Vero cytotoxin A subunit and B subunit have been adopted in the cytotoxic expression of Vero.Utilize the msbB gene that this tetracycline induction type BRP Vero cytotoxin AB is cloned into a kind of carrier that is used for chromosomal integration.24.1. The structure of carrier24.1.1. The amplification of AB and clone

Utilize PCR method to produce Vero cytotoxin AB (AB), the primer of use is as follows: H19B-7: forward primer: 5 '-GTGTCCATGGCTAAAACATTATTAATAGCTGCATCGC-3 ' (SEQ ID NO:37); And QSTX-R1: reverse primer: 5 '-GTGTCTGCAGAACTGACTGAATTGAGATG-3 ' (SEQ IDNO:38)

These primers also contain outside NcoI (5 ') and PstI (3 ') restriction endonuclease site, are used for being cloned into NcoI and the PstI site of ptrc99a.24.1.2. The amplification of TetBRP and clone

TetBRP-AB is building up among the intermediate carrier pSP72-F6/R6.Utilize PCR method to produce TetBRP, the primer of use is as follows: Tet-5 ': forward primer 5 '-GTGTAGATCTTTAAGACCCACTTTCACATTTAAGTTG-3 ' (SEQ ID NO:39) and BRP-TET-3 ': reverse primer 5 '-CACAGGATCCTTACTGAACCGCGATCCCCG-3 ' (SEQ ID NO:40).These primers contain BglII (5 ') and BamHI (3 ') restriction endonuclease site, are used for being cloned into the BglII and the BamHI site of pSP72-F6/R6 carrier.24.1.3. With the AB sub-clone in pSP72-F6/R6-TetBRPWith BamHI and AvaI restriction endonuclease digestion ptrc99A-AB,, be used for being inserted into equally by the pSP72-F6/R6-TetBRP of BamHI and the digestion of AvaI restriction endonuclease to obtain AB.The pSP72F6/R6 carrier contains multiple restriction endonuclease site, can be used to clone the part β-gal gene with lacZ-α reverse complemental.On 0.8%1 * TAE agarose gel, analyze carrier (pSP72F6/R6-TetBRP) and AB insertion sequence, carry out purification with the Qiagen gel extraction kit then.With T4 ligase connection carrier and insertion sequence, reusable heat shock method is transformed in the e.colidh5.Then cell is layered on the LB flat board that contains 100 μ g/ml Amp and 40 μ g/ml X-gal.Screening has the positive colony of amicillin resistance and functional β-gal gene (it is blue that positive colony is).24.1.4. With the TetBRP-AB sub-clone in pCDV442

With NotI and SfiI restriction endonuclease digestion pSP72F6/R6-TetBRP-AB, be used for sub-clone to equally by the pCVD442 carrier of NotI and SfiI digestion with restriction enzyme.24.1.5. The msbB chromosome vector

Utilize suicide vector pCVD442 (Donnenberg and Kaper, 1991, Infection and Immunity 59:4310-4317) a kind of carrier that can carry out homologous recombination of structure by the chromosome of DmsbB gene and VNP20009 bacterial strain (in international monopoly WO99/13053, having another name called YS1626).The excalation that in VNP20009, has msbB5 ' and 3 ' end regions, design PCR primer with produce respectively these two kinds of products (msbB-5 ': forward 5 '-GTG TGA GCT CGA TCA ACC AGC AAG CCG TTA ACC CTC TGA C-3 ' (SEQID NO:41) and reverse 5 '-GTG TGC ATG CGG GGG GCC ATA TAG GCC GGGGAT TTA AAT GCA AAC GTC CGC CGA AAC GCC GAC GCA C-3 ' (SEQ IDNO:42); And msbB-3 ': forward 5 '-GTG TGC ATG CGG GGT TAA TTA AGGGGG CGG CCG CGT GGT ATT GGT TGA ACC GAC GGT GCT CAT GAC ATCGC-3 ' (SEQ ID NO:43) and reverse 5 '-GTG TCT CGA GGA TAT CAT TCT GGCCTC TGA CGT TGT G-3 ' (SEQ ID NO:44)).These primers also contain outside SacI (5 ') and AvaI (3 ') restriction endonuclease site, can be used to be cloned among the SacI and SalI site of pCVD442, after these two kinds of fragments connect by common SphI site, can produce inner NotI, PacI, SphI, SfiI, SwaI and DraI, can be used for dna fragmentation is cloned among the DmsbB, to obtain not contain the stable chromosomal integration (Figure 31) of antibiotic resistance.This carrier is called as pCVD442-msbB (with reference to Figure 32 and Figure 33).

For Tet-BRP-AB is cloned among the pCVD442-msbB, with Tet-BRP-AB plasmid DNA restrictive diges-tion and be purified into suitable DNA, reuse T4 ligase connects two kinds of compositions.Transform DH5 1pir with the coupled reaction thing then, and screen bacterium colony according to existence and the orientation of Tet-BRP-AB.Tet-BRP-AB is transformed in the SM101pir bacterial strain (Donnenbergand Kaper, 1991, see above), the gained plasmid is called pCVD442-Tet-BRP-AB.Utilize the PCR method screening to contain the SM101pir bacterium colony of Tet-BRP-AB gene, and select the positive SM101pir bacterium colony conduct and the bonded donor of Salmonella bacterial strain of a pCVD442-Tet-BRP-AB.Utilize standard method (Davis, R.W., Botstein, D., and Roth, J.R.1980, Advanced Bacterial GeneticsCold Spring HarborLaboratory Press, Cold Spring Harbor) will contain SM101pir and Salmonella YS50101 bacterial strain (tetracyclin resistance YS82 bacterial strain (the Low et al. of pCVD442-Tet-BRP-AB, 1999, see above) a kind of natural derivative, have stronger DifcoMacConkey agar resistance) combination, and at the dull and stereotyped enterprising row filter that contains 50 μ g/ml Carbenicillins (carb) and 300 μ g/ml streptomycins (strep).PCR detects the pCVD442-Tet-BRP-AB gene among the gained YS50102-pCVD442-Tet-BRP-AB clone.24.2. Chromosomal integration pCVD442-Tet-BRP-AB is transferred to 41.2.9 (YS1646) In, to produce the 41.2.9-Tet-RRP-AR bacterial strain

With the YS50102-Tet-BRP-AB bacterial strain is donor, with phage P22 (HT105/1int-201 mutant; Davis et al., 1980) transduce, make 41.2.9 obtain the Carbenicillin resistance.Utilize pCVD442 to go up the bla of existence and the carb that the sacB genescreen contains DmsbB and DmsbB-Tet-BRP-AB gene ^r(or amp ^r) suc ^sBacterial strain, this bacterial strain be called 41.2.9-pCVD-Tet-BRP-AB-1 (Figure 33, #3).The 41.2.9-Tet-BRP-AB-1 bacterial strain is layered on the LB sucrose flat board, does not contain the DmsbB gene but the suc of reservation DmsbB-Tet-BRP-AB gene with screening ^rCarb ^sDerivant adopts above Donnenberg and Kaper here, and 1991 method does not just contain NaCl in the LB-sucrose agar plate, and is that flat board is incubated in 30 ℃.After growing bacterium colony on these flat boards, it is transferred on the msbB flat board by original grid, and duplicate is tiled on the flat board that contains Carbenicillin or sucrose, to detect the clone who does not contain antibiotic and sucrose labelling.With having the Tet-BRP-AB gene in the PCR method checking institute DCRP.So the derivant that obtains contains chromosomal integration Tet-BRP-AB, and does not have sucrose responsive type and Carbenicillin resistance, and this bacterial strain is called 41.2.9-Tet-BRP-Vero cytotoxin AB.

Utilize standard the LDH cytotoxicity assay (Cytotox96 , Promega, Madison, Wisconsin) cytotoxicity to 41.2.9-Tet-BRP-Vero cytotoxin AB carries out vitro detection.Cytotoxic clone 26 of Vero and clone's 31 toxicity characteristic is expressed in the explanation of Figure 34 result displayed.Compare with handling without tetracycline, clone 26 and clone 31 after handling with tetracycline have obviously higher cytotoxic percentage.25. Embodiment: by the bacterial expression hemolysin that is oriented to tumor

Following embodiment explanation, the antibacterial that is oriented to tumor can composing types through processing or dissolved blood protein such as inducible expression hemolysin.

As everyone knows, hemolysin be can splitting erythrocyte cytotoxic protein (reference, for example, Beutin, 1991, Med.Microbiol.Immunol 180:167-182).SheA (Genbank numbers ECO238954) is the reticent hemolysin (Fernandez et al., 1998, FEMSMicriobiol Lett 168:85-90) of a kind of improper expression of existing in most of wild-type e. colis.Under Standard PC R condition, from wild-type e. coli (2507 bacterial strains, Yale University E.coli Genetic Stock Center), clone SheA and (have another name called hlyE; Genbank numbers U57430), the primer of use is as follows: (forward) 5 '-TTTTTTCCAT GGCTATTATG ACTGAAATCG TTGCAGATAAAACGG-3 ' (SEQ ID NO:45) and (oppositely) 5 '-TTTTTTAAGC TTCCCGGGTCAGACTTCAGG TACCTCAAG AGTGTC-3 ' (SEQ ID NO:46).The PCR product cloning of correct size is arrived among the NcoI and HindIII site of ptrc99a (Pharmacia), make it be subjected to part composing type trc promoter regulation.In addition also with PCR product cloning (it is described to see above) in the tet-bgal-Z-term carrier of shearing with NcoI and EcoRY.With plasmid transformation escherichia coli DH5 α (Gibco), be layered on then on the blood agar that adds or do not add 0.2 μ g/ml tetracycline (the tryptone bean peptone agar that contains 5% Sanguis caprae seu ovis, Biomerieux, Lombard, IL).Picking contains the hemolytic limpid dizzy positive bacterium colony of expression in periphery of bacterial colonies.Positive bacteria is dropped into the plasmid purification of column criterion, transform Salmonella YS501 and this screening of swooning again with plasmid then.

Figure 35 (2A and 2B) shows the dizzy formation of the composing type of trc99a construct, adds or do not add tetracycline all can observe dizzy this moment.Figure 35 (3A and 3B) shows the dizzy formation of the tetracycline dependent form of tetracycline promoters driven SheA, and do not add tetracycline and then do not form dizzy this moment.These presentation of results, the antibacterial that is oriented to tumor promptly can the constitutive expression dissolved blood proteins, also can the inducible expression dissolved blood protein.26. Embodiment: by the bacterial expression methioninase that is oriented to tumor

Following embodiment explanation, Salmonella etc. are oriented to the attenuated bacteria of tumor can express methioninase through processing.

Methioninase is a kind of enzyme of degraded methionine, and methionine is the required a kind of essential amino acids of tumor growth.Utilize the administration of the administration of purification methioninase or coding DNA of methioninase or viral vector to suppress existing describe (the international monopoly WO00/29589 of Xu and Tan) of method of tumor growth.But Xu and Tan does not mention the method for sending methioninase with the tumour-specific bacteria carrier, does not point out to treat the methioninase that needs use a large amount of with purifying protein yet.The new method that methioninase directly can be delivered to tumor is to express this kind of enzyme with the antibacterial that is oriented to tumor.

Utilize following primer to produce the Pneudomas putida methioninase of Genbank numbering L43133: forward: METH-XHOI 5 '-CCGCTCGAGATGCACGGCTCCAACAAGCTCCCA-3 ' (SEQID NO:47); Oppositely: METH-BAM 5 '-CGCGGATCCTTAGGCACTCGCCTTGAGTGCCTG-3 ' (SEQ IDNO:48)

Is that template goes out the methionine enzyme sequence with above-mentioned primer amplification by PCR method with the single bacterium colony of pseudomonas, and the condition of PCR is as follows: 1 circulation: 94 ℃ 5 minutes, be 35 circulations then: 94 ℃ 1 minute, 60 ℃ 1 minute, 72 ℃ 2 minutes.The final amplification step of PCR reaction is 72 ℃, 10 minutes.On 0.8%1 * TAE agarose gel, analyze the PCR product, and identify and have methioninase expection size (～1196bp) PCR product.Downcut this band from glue, carry out purification with the Qiagen gel extraction kit then.

Methioninase gene with Restriction Enzyme XhoI and BamHI digestion pSP72 carrier and above-mentioned gel separation purification.On 0.8%1 * TAE agarose gel, the carrier and the methioninase gene of digestion are analyzed then.Downcut the digestion product that is equivalent to linearized vector and methionine enzymic digestion gene from gel, and carry out purification with Qiagen gel extraction agent box.Connect linearized vector and insertion sequence (methioninase) with the T4 ligase.Reusable heat shock method will connect mixture and be transformed in the e.colidh5.Then the cell that recovers is layered on the LB culture medium that contains 100 μ g/ml ampicillin (Amp), contains the cell of complete pSP72 carrier with screening.Picking Amp resistance bacterium colony, and prepare plasmid with Qiagen mini-prep test kit, digest with EcoRI and BspHI Restriction Enzyme then, to confirm to contain existing of methioninase gene pSP72 carrier.No. 9 clone delivered to Yale sequencyingFacility, and Yale University School of Medicine checks order.Adopt SP6 (forward) and T7 (oppositely) sequencing primer during order-checking.The result shows, except that termination codon TGA is changed to the TAA all the other sequences and methionine enzyme sequence 100% coupling of delivering when the PCR.

The active mensuration of methioninase can adopt Hori et al., and 1996, the methionine enzyme assay of describing among the CancerResearch 56:2116-2122.27. Embodiment: in being oriented to the attenuated bacteria of tumor, express apoptosis with TAT fusant form Fibroin

Following embodiment explanation, the attenuated bacteria that is oriented to tumor can be expressed through processing and secrete the fusion rotein that contains effector molecule and transport peptide such as TAT, feeler foot homeodomain, VP22 and card ripple west FGF MTS etc.27.1. The structure of the plain carrier of TAT-apoptosis

Known canary virus (CAV) of sending by adenovirus vector but the apoptosis of albumen apoptosis element inducing tumor cell (reference, for example, Noteborn et al., 1999, Gene Therapy6:882-892).

Merge with the apoptosis fibroin and from the proteic a kind of peptide of human immunodeficiency virus (HIV) TAT, to produce a kind of can in salmonella cell matter, transcribing, thereby the nucleus that can be transported to tumor cell then causes the albumen (reference of apoptosis, for example, Schwartze et al., 1999, Science 285:1569-1572).Also find in addition, TAT albumen fusant and poly histidine (six polyhistidyls) still have function after merging, and the poly histidine can increase positive charge, thereby help protein purification (Schwartze et al., 1999, see above), so also produced the TAT-apoptosis plain fusion protein (Figure 36 A and B) that contains six polyhistidyls and do not contain six polyhistidyls.In addition, can also produce the TAT-apoptosis plain fusion protein (Figure 36 A and C) that contains the OmpA-8L signal sequence and do not contain the OmpA-8L signal sequence.

Utilize the plain and six polyhistidyl apoptosis elements of overlapping oligonucleotide assembling apoptosis.PCR,：TAP1：5’-GATCCCATGG CTTATGGCAG AAAAAAACGC CGTCAGCGCCGTCGCATGAA CGCGCTGCAG GAAGATACCC CGCCGGGCCC GTCCACCGTGTTTCGCCCGC CG-3’ ( SEQ ID NO：49 ) TAP2：5’-GGGACAGGGT GATGGTGATG CCCGCGATGC CGATGCGGATTTCGCGGCAA TGCGGGGTTT CCAGCGGGCG GGAGGAGGTC GGCGGGCGAAACACGGTGGA CGG-3’ ( SEQ ID NO：50 ) TAP3：5’-GGCATCGCGG GCATCACCAT CACCCTGTCC CTGTGCGGCTGCGCGAACGC GCGCGCGCCG ACCCTGCGCT CCGCGACCGC GGATAACTCCGAAAACACCG GC-3’ ( SEQ ID NO：51 ) TAP4：5’-GCGATATTCG GACGGATCGC AGGAGCGTTT TTTGGACGGCGGTTTCGGCT GATCGGTGCG CAGATCCGGG ACGTTTTTAA AGCCGGTGTTTTCGGAGTTA TCCGCGGTCG C-3’ ( SEQ ID NO：52 ) TAP5：5’-CCTGCGATCC GTCCGAATAT CGCGTCTCCG AACTGAAAGAATCCCTGATC ACCACCACCC CGTCCCGCCC GCGCACCGCC CGCCGCTGCATCCGCCTCTG AAAGCTTCAT G-3’ ( SEQ ID NO：53 ) TAP6：5’-CATGAAGCTT TCAGAGGCGG ATGCAGCGGC GGGCGGTGCG C-3’ ( SEQ ID NO：54 )

With TAP 2-TAP6 oligonucleotide and TAP6H1 oligonucleotide (5 '-GATCCCATGGCTCATCACCA TCACCACCAT TATGGCCGCA AAAAACGCCG TCAGCGCCGTCGCATGAACG CGCTGCAGGA AGATACCCCG CCGGGCCC-3 '; SEQ ID NO:55) generation contains the nucleic acid sequence encoding of the TAT-apoptosis plain fusion protein of six polyhistidyls.By PCR method TAP6 oligonucleotide and omp8LF1 oligonucleotide (5 '-GATCCCATGGCTAAAAAGAC GGCTCTGGCG CTTCTGCTCT TGCTGTTAGC GCTGACTAGTGTAGCGCAGG CCTATGGCCG CAAAAAACGC CGTCAGCGCC-3 '; SEQ ID NO:56) from the PCR product of TAP1-TAP6, obtains to contain the nucleic acid sequence encoding of the TAT-apoptosis plain fusion protein of OmpA8L.

Every kind of oligonucleotide is made into the liquid storage that concentration is 4 μ M.The PCR reaction pearl (Pharmacia, Ready-to-go beads) of premix is adopted in reaction, and every kind of oligonucleotide uses 2 μ l.PCR reaction comprises 1 circulation: 95 ℃ 5 minutes; 35 circulations: 95 ℃ 1 minute, 60 ℃ 1 minute, 72 ℃ 1 minute; With 1 circulation: 72 ℃ 10 minutes.Then the PCR product is carried out phenol/chloroform extracting, ethanol precipitation, weight is water-soluble, and carries out restrictive diges-tion with NcoI and HindIII.Utilize gel electrophoresis method that the PCR product of restrictive diges-tion is analyzed, downcut the product (TAT-apoptosis element and six polyhistidyls-TAT-apoptosis element are about 420bp and 450bp respectively) with correct size from gel, the Protocols in Molecular Biology with standard separates then.These products are connected with the ptrc99a (Pharmacia) of HindIII digestion with NcoI, promptly obtain the plain construct of ptrc99a-TAT-apoptosis.The DNA sequence that obtains is respectively correct TAT-apoptosis element (Figure 37) and six polyhistidyls-TAT-apoptosis element (Figure 38).27.2. The proof of plain secretion of TAT-apoptosis and picked-up

Transform the attenuated bacteria that is oriented to tumor by standard method known in the art (as heat shock or electroporation method) with the plain construct of ptrc99a-TAT-apoptosis, in culture medium, cultivate then.Utilize in technology well known by persons skilled in the art (as western blot analysis or ELISA) the bacterial detection culture supernatants and whether have TAT-apoptosis element.If have TAT-apoptosis element in the supernatant of confirmation bacterial cultures, then with the supernatant of bacterial cultures and mammalian cell (as NIG3T3, CHO, 293 and the 293T cell) insulation altogether, and utilize the plain algoscopy of apoptosis well known by persons skilled in the art to confirm to have TAT-apoptosis element in the cell.27.3. The proof of the plain picked-up of TAT-apoptosis in the tumor

With the attenuated bacteria that is oriented to tumor of expressing TAT-apoptosis element or apoptosis element through processing the B16 tumor model is carried out intravenous administration.With after antibacterial administration a couple of days, put to death mice and also measure the organ weight.Utilize apoptosis assay method well known by persons skilled in the art (to divide ladder and fluorescein original position cell death detection kit (Boehringer Mannheim, Mannheim, Germany)) to detect the existence and the location of interior TAT-apoptosis element of tumor or apoptosis element as DNA.Measure the size of tumor in addition, to determine the anti-tumor activity of TAT-apoptosis element.Also tumor homogenate and bed board are cultivated in addition, form location (c.f.u.) to measure colony.28. The combination of embodiment: VNP20009 and chemotherapeutics is to the effectiveness of M27 pulmonary carcinoma growth in the mice

Following embodiment explanation, the attenuated bacteria that is oriented to tumor and the combination medicine-feeding of chemotherapeutics can be worked in coordination with and be suppressed or the growth of solid tumors such as addition inhibition pulmonary carcinoma.28.1. The combination of the combination of VNP20009 and cyclophosphamide or VNP20009 and ametycin Effectiveness to M27 pulmonary carcinoma growth in the mice

In 37 ℃ of M27 Mus lung carcinoma cells (1 * 10 that liquid nitrogen is preserved ⁶/ ml * 1ml) melt fast makes its recovery, then in 37 ℃, 5%CO ₂Condition under cultivate and contain in the DMEM culture medium of 10% hyclone (FCS) at 10ml.After cell goes down to posterity for twice, the M27 cell of logarithmic (log) phase is separated by trypsinization, 1 * PBS cleans, then with 2.5 * 10 ⁶The concentration of cell/ml is resuspended among 1 * PBS, is used for implantation tumour.The 0th day, with the M27 cell suspending liquid implant 100 C57BL/6 mices (female, 8 ages in week, 20g; 5 * 10 ⁵Cell/Mus) under the right ribbed hide.Mice is divided into 10 groups at random, 10 every group.

Dilution process by standard is diluted to 5 * 10 with 1 * PBS with Salmonella VNP20009 bacterial strain ⁶CFU/ml.In the time of the 12nd day, according to the Salmonella (1 * 10 of following table 6 usefulness 0.2ml dilution ⁶The CFU/ Mus) every mice is carried out intravenous administration.In order to determine the actual injection amount of antibacterial, with 5 * 10 ⁶The bacterial suspension of CFU/ml further is diluted to 1 * 10 ³CFU/ml, and be layered on (MsbB flat board on the Nutrient agar; International monopoly WO99/13053).Colony counting to forming in second day.

According to following table 7 usefulness ametycins (Sigma) and cyclophosphamide (Sigma) mice is carried out administration.In the time of the 22nd day, the combination medicine-feeding group is carried out 2 administrations of ametycin, but the group of only handling with ametycin there are not 2 administrations owing to tumor is excessive.When in VNP20009+ cyclophosphamide processed group, observing serious toxic reaction, to only handling or respectively organizing Cipro (Bayer Inc., West Haven, CT) processing that mice carries out 200mpk with what the VNP20009+ chemotherapeutics was handled with VNP20009.Measure gross tumor volume 2 times weekly, finish up to experiment.Observe behavior, outward appearance and the mortality rate of animal every day.Mice remains in the constant temperature laboratory of cleaning.The lodge pad is changed weekly 2 times, and provides competent food and drinking water for mice.

Table 7

Group	Mice quantity
Group	Mice quantity	Do not handle contrast	????10
3mpk, ametycin, i.v., the 15th day	????10	Do not handle contrast	????10
3mpk, ametycin, i.v., the 15th day	????10	5mpk, ametycin, i.v., the 15th day	????10
150mpk, cyclophosphamide, i.p., the 15th day	????10	5mpk, ametycin, i.v., the 15th day	????10
150mpk, cyclophosphamide, i.p., the 15th day	????10	200mpk, cyclophosphamide, i.p., the 15th day	????10
?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day	????10	200mpk, cyclophosphamide, i.p., the 15th day	????10
?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day	????10	?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day+3mpk, ametycin, i.v., the 15th and the 22nd day	????10
?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day+5mpk, ametycin, i.v., the 15th and the 22nd day	????10		????10
	????10	?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day+the 150mpk cyclophosphamide, i.p., the 15th day	????10
?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day+the 200mpk cyclophosphamide, i.p., the 15th day	????10		????10

As shown in figure 39, VNP20009+ cyclophosphamide combined treatment only is better than with VNP20009 to the inhibition of M27 pulmonary carcinoma growth or only handles with cyclophosphamide.As shown in figure 40, VNP20009+ ametycin combination is handled inhibition to the growth of M27 pulmonary carcinoma and only is better than and handles with ametycin.But the inhibition that the combination of VNP20009+ ametycin is handled the growth of M27 pulmonary carcinoma is not better than only with VNP20009 processing (Figure 40).These results show, the combination medicine-feeding that is oriented to the attenuated bacteria of tumor and chemotherapeutics can be worked in coordination with and be suppressed or addition suppresses the growth of solid tumors such as pulmonary carcinoma.28.2. The combination of VNP20009 and cisplatin is to the effectiveness of M27 pulmonary carcinoma growth in the mice

In 37 ℃ of M27 Mus lung carcinoma cells (1 * 10 that liquid nitrogen is preserved ⁶/ ml * 1ml) melt fast makes its recovery, then in 37 ℃, 5%CO ₂Condition under cultivate and contain in the DMEM culture medium of 10% hyclone (FCS) at 25ml.After cell goes down to posterity for twice, the M27 cell (saturation of about 90-95%) of logarithmic (log) phase is separated by trypsinization, 1 * PBS cleans, then with 2.5 * 10 ⁶The concentration of cell/ml is resuspended among 1 * PBS, is used for implantation tumour.The 0th day, with M27 cell suspending liquid (0.2ml) implant 36 C57BL/6 mices (female, 8 ages in week, 20g; 5 * 10 ⁵Cell/Mus) under the right ribbed hide.With the mice random packet, 9 every group.

Dilution process by standard is diluted to 5 * 10 with 1 * PBS with Salmonella VNP20009 bacterial strain ⁶CFU/ml.In the time of the 12nd day, according to following table 8 usefulness 0.2ml Salmonellas (1 * 10 ⁶The CFU/ Mus) every mice is carried out the tail vein administration.In order to determine the actual injection amount of antibacterial, with 5 * 10 ⁶The bacterial suspension of CFU/ml further is diluted to 1 * 10 ³CFU/ml, and be layered on the MsBb flat board.Colony counting to forming in second day.

In the time of the 14th day, antibacterial injection just delivered medicine to mice (following table 8) with cisplatin after 2 days.With normal normal saline cisplatin is diluted to 0.5mg/ml before the administration.Measure gross tumor volume 2 times weekly, finish up to experiment.Observe behavior, outward appearance and the mortality rate of animal every day.Mice remains in the constant temperature laboratory of cleaning.The nest pad of animal is changed weekly 2 times, and provides competent food and drinking water for mice.

Table 8

Group	Mice quantity
Group	Mice quantity	Contrast (not handling)	????9
?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day	????9	Contrast (not handling)	????9
?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day	????9	The 5mpk cisplatin, i.p.qw * 2, the 14 and the 19th day	????9
?VNP20009，1×10 ⁶/ Mus, i.v., the 12nd day+the 5mpk cisplatin, i.p.qw * the 2, the 14, the 19th and the 33rd day	????9	The 5mpk cisplatin, i.p.qw * 2, the 14 and the 19th day	????9

As shown in figure 41, VNP20009+ cisplatin combined treatment only is better than with VNP20009 to the inhibition of M27 pulmonary carcinoma growth or only uses cisplatin treated.These results show, the combination medicine-feeding that is oriented to chemotherapeutics such as the attenuated bacteria of tumor and cisplatin can be worked in coordination with and be suppressed or addition suppresses the growth of solid tumors such as pulmonary carcinoma.

The special embodiment that scope of the present invention is not limited to describe in the literary composition.In fact, those skilled in the art as can be seen, the present invention also has multiple different variation except that mentioned above from above description and accompanying drawing.These variations will be included within the scope of claims.

Quoted a lot of publications in the literary composition, all complete introducing of its disclosure, for your guidance.

Sequence table

＜110〉Vion Pharmaceuticals Inc.

＜120〉be used for compositions and the method for effector molecule targeted delivery to tumor

<130>8002-059-228

<150>60/157,581

<151>1999-10-04

<150>60/157,637

<151>1999-10-04

<160>61

<170>FastSEQ?for?Windows?Version?3.0

<210>1

<211>26

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>1gaagatcttc?cggaggaggg?gaaatg???????????????????????????????????????????26

<210>2

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>2cgggatccga?gctcgagggc?ccgggaaagg?at?ctaagaag?atcc??????????????????????44

<210>3

<211>477

<212>DNA

＜213〉people (Homo sapiens)

<220>

<221>CDS

<222>(1)...(474)

<400>3atg?gta?cgt?agc?tcc?tct?cgc?act?ccg?tcc?gat?aag?ccg?gtt?gct?cat??????48Met?Val?Arg?Ser?Ser?Ser?Arg?Thr?Pro?Ser?Asp?Lys?Pro?Val?Ala?His?1???????????????5???????????????????10??????????????????15gta?gtt?gct?aac?cct?cag?gca?gaa?ggt?cag?ctg?cag?tgg?ctg?aac?cgt???????96Val?Val?Ala?Asn?Pro?Gln?Ala?Glu?Gly?Gln?Leu?Gln?Trp?Leu?Asn?Arg

20??????????????????25??????????????????30cgc?gct?aac?gcc?ctg?ctg?gca?aac?ggc?gtt?gag?ctc?cgt?gat?aac?cag??????144Arg?Ala?Asn?Ala?Leu?Leu?Ala?Asn?Gly?Val?Glu?Leu?Arg?Asp?Asn?Gln

35??????????????????40??????????????????45ctc?gtg?gta?cct?tct?gaa?ggt?ctg?tac?ctg?atc?tat?tct?caa?gta?ctg??????192Leu?Val?Val?Pro?Ser?Glu?Gly?Leu?Tyr?Leu?Ile?Tyr?Ser?Gln?Val?Leu

50??????????????????55??????????????????60ttc?aag?ggt?cag?ggc?tgc?ccg?tcg?act?cat?gtt?ctg?ctg?act?cac?acc??????240Phe?Lys?Gly?Gln?Gly?Cys?Pro?Ser?Thr?His?Val?Leu?Leu?Thr?His?Thr?65??????????????????70??????????????????75??????????????????80atc?agc?cgt?att?gct?gta?tct?tac?cag?acc?aaa?gtt?aac?ctg?ctg?agc??????288Ile?Ser?Arg?Ile?Ala?Val?Ser?Tyr?Gln?Thr?Lys?Val?Asn?Leu?Leu?Ser

85??????????????????90??????????????????95gct?atc?aag?tct?ccg?tgc?cag?cgt?gaa?act?ccc?gag?ggt?gca?gaa?gcg??????336Ala?Ile?Lys?Ser?Pro?Cys?Gln?Arg?Glu?Thr?Pro?Glu?Gly?Ala?Glu?Ala

100?????????????????105?????????????????110aaa?cca?tgg?tat?gaa?ccg?atc?tac?ctg?ggt?ggc?gta?ttt?caa?ctg?gag??????384Lys?Pro?Trp?Tyr?Glu?Pro?Ile?Tyr?Leu?Gly?Gly?Val?Phe?Gln?Leu?Glu

115?????????????????120?????????????????125aaa?ggt?gac?cgt?ctg?tcc?gca?gaa?atc?aac?cgt?cct?gac?tat?cta?gat??????432Lys?Gly?Asp?Arg?Leu?Ser?Ala?Glu?Ile?Asn?Arg?Pro?Asp?Tyr?Leu?Asp

130?????????????????135?????????????????140ttc?gct?gaa?tct?ggc?cag?gtg?tac?ttc?ggt?att?atc?gca?ctg??????????????474Phe?Ala?Glu?Ser?Gly?Gln?Val?Tyr?Phe?Gly?Ile?Ile?Ala?Leu145?????????????????150?????????????????155taa??????????????????????????????????????????????????????????????????477

<210>4

<211>158

<212>PRT

＜213〉people (Homo sapiens)

<400>4Met?Val?Arg?Ser?Ser?Ser?Arg?Thr?Pro?Ser?Asp?Lys?Pro?Val?Ala?His?1???????????????5??????????????????10??????????????????15Val?Val?Ala?Asn?Pro?Gln?Ala?Glu?Gly?Gln?Leu?Gln?Trp?Leu?Asn?Arg

20??????????????????25??????????????????30Arg?Ala?Asn?Ala?Leu?Leu?Ala?Asn?Gly?Val?Glu?Leu?Arg?Asp?Asn?Gln

35??????????????????40??????????????????45Leu?Val?Val?Pro?Ser?Glu?Gly?Leu?Tyr?Leu?Ile?Tyr?Ser?Gln?Val?Leu

50??????????????????55??????????????????60Phe?Lys?Gly?Gln?Gly?Cys?Pro?Ser?Thr?His?Val?Leu?Leu?Thr?His?Thr65??????????????????70??????????????????75??????????????????80Ile?Ser?Arg?Ile?Ala?Val?Ser?Tyr?Gln?Thr?Lys?Val?Asn?Leu?Leu?Ser

85??????????????????90??????????????????95Ala?Ile?Lys?Ser?Pro?Cys?Gln?Arg?Glu?Thr?Pro?Glu?Gly?Ala?Glu?Ala

100?????????????????105?????????????????110Lys?Pro?Trp?Tyr?Glu?Pro?Ile?Tyr?Leu?Gly?Gly?Val?Phe?Gln?Leu?Glu

115?????????????????120?????????????????125Lys?Gly?Asp?Arg?Leu?Ser?Ala?Glu?Ile?Asn?Arg?Pro?Asp?Tyr?Leu?Asp

130?????????????????135?????????????????140Phe?Ala?Glu?Ser?Gly?Gln?Val?Tyr?Phe?Gly?Ile?Ile?Ala?Leu145?????????????????150?????????????????155

<210>5

<211>28

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>5ccgacgcgtt?gacacctgaa?aactggag??????????????????????????????????????????28

<210>6

<211>29

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>6ccgacgcgtg?aaaggatctc?aagaagatc??????????????????????????????????????????29

<210>7

<211>543

<212>DNA

＜213〉artificial sequence

<220>

＜223〉fusion constructs

<221>CDS

<222>(1)...(540)

<400>7atg?aaa?aag?aca?gct?atc?gcg?att?gca?gtg?gca?ctg?gct?ggt?ttc?gct???????48Met?Lys?Lys?Thr?Ala?Ile?Ala?Ile?Ala?Val?Ala?Leu?Ala?Gly?Phe?Ala?1???????????????5???????????????????10??????????????????15acc?gta?gcg?cag?gcc?cat?atg?gta?cgt?agc?tcc?tct?cgc?act?ccg?tcc???????96Thr?Val?Ala?Gln?Ala?His?Met?Val?Arg?Ser?Ser?Ser?Arg?Thr?Pro?Ser

20??????????????????25??????????????????30gat?aag?ccg?gtt?gct?cat?gta?gtt?gct?aac?cct?cag?gca?gaa?ggt?cag??????144Asp?Lys?Pro?Val?Ala?His?Val?Val?Ala?Asn?Pro?Gln?Ala?Glu?Gly?Gln

35??????????????????40??????????????????45ctg?cag?tgg?ctg?aac?cgt?cgc?gct?aac?gcc?ctg?ctg?gca?aac?ggc?gtt??????192Leu?Gln?Trp?Leu?Asn?Arg?Arg?Ala?Asn?Ala?Leu?Leu?Ala?Asn?Gly?Val

50??????????????????55??????????????????60gag?ctc?cgt?gat?aac?cag?ctc?gtg?gta?cct?tct?gaa?ggt?ctg?tac?ctg??????240Glu?Leu?Arg?Asp?Asn?Gln?Leu?Val?Val?Pro?Ser?Glu?Gly?Leu?Tyr?Leu?65??????????????????70??????????????????75??????????????????80atc?tat?tct?caa?gta?ctg?ttc?aag?ggt?cag?ggc?tgc?ccg?tcg?act?cat??????288Ile?Tyr?Ser?Gln?Val?Leu?Phe?Lys?Gly?Gln?Gly?Cys?Pro?Ser?Thr?His

85??????????????????90??????????????????95gtt?ctg?ctg?act?cac?acc?atc?agc?cgt?att?gct?gta?tct?tac?cag?acc??????336Val?Leu?Leu?Thr?His?Thr?Ile?Ser?Arg?Ile?Ala?Val?Ser?Tyr?Gln?Thr

100?????????????????105?????????????????110aaa?gtt?aac?ctg?ctg?agc?gct?atc?aag?tct?ccg?tgc?cag?cgt?gaa?act??????384Lys?Val?Asn?Leu?Leu?Ser?Ala?Ile?Lys?Ser?Pro?Cys?Gln?Arg?Glu?Thr

115?????????????????120?????????????????125ccc?gag?ggt?gca?gaa?gcg?aaa?cca?tgg?tat?gaa?ccg?atc?tac?ctg?ggt??????432Pro?Glu?Gly?Ala?Glu?Ala?Lys?Pro?Trp?Tyr?Glu?Pro?Ile?Tyr?Leu?Gly

130?????????????????135?????????????????140ggc?gta?ttt?caa?ctg?gag?aaa?ggt?gac?cgt?ctg?tcc?gca?gaa?atc?aac??????480Gly?Val?Phe?Gln?Leu?Glu?Lys?Gly?Asp?Arg?Leu?Ser?Ala?Glu?Ile?Asn145?????????????????150?????????????????155?????????????????160cgt?cct?gac?tat?cta?gat?ttc?gct?gaa?tct?ggc?cag?gtg?tac?ttc?ggt??????528Arg?Pro?Asp?Tyr?Leu?Asp?Phe?Ala?Glu?Ser?Gly?Gln?Val?Tyr?Phe?Gly

165?????????????????170?????????????????175att?atc?gca?ctg?taa??????????????????????????????????????????????????543Ile?Ile?Ala?Leu

180

<210>8

<211>180

<212>PRT

＜213〉artificial sequence

<400>8Met?Lys?Lys?Thr?Ala?Ile?Ala?Ile?Ala?Val?Ala?Leu?Ala?Gly?Phe?Ala?1???????????????5??????????????????10??????????????????15Thr?Val?Ala?Gln?Ala?His?Met?Val?Arg?Ser?Ser?Ser?Arg?Thr?Pro?Ser

20??????????????????25??????????????????30Asp?Lys?Pro?Val?Ala?His?Val?Val?Ala?Asn?Pro?Gln?Ala?Glu?Gly?Gln

35??????????????????40??????????????????45Leu?Gln?Trp?Leu?Asn?Arg?Arg?Ala?Asn?Ala?Leu?Leu?Ala?Asn?Gly?Val

50??????????????????55??????????????????60Glu?Leu?Arg?Asp?Asn?Gln?Leu?Val?Val?Pro?Ser?Glu?Gly?Leu?Tyr?Leu65??????????????????70??????????????????75??????????????????80Ile?Tyr?Ser?Gln?Val?Leu?Phe?Lys?Gly?Gln?Gly?Cys?Pro?Ser?Thr?His

85??????????????????90??????????????????95Val?Leu?Leu?Thr?His?Thr?Ile?Ser?Arg?Ile?Ala?Val?Ser?Tyr?Gln?Thr

100?????????????????105?????????????????110Lys?Val?Asn?Leu?Leu?Ser?Ala?Ile?Lys?Ser?Pro?Cys?Gln?Arg?Glu?Thr

115?????????????????120?????????????????125Pro?Glu?Gly?Ala?Glu?Ala?Lys?Pro?Trp?Tyr?Glu?Pro?Ile?Tyr?Leu?Gly

130?????????????????135?????????????????140Gly?Val?Phe?Gln?Leu?Glu?Lys?Gly?Asp?Arg?Leu?Ser?Ala?Glu?Ile?Asn145?????????????????150?????????????????155?????????????????160Arg?Pro?Asp?Tyr?Leu?Asp?Phe?Ala?Glu?Ser?Gly?Gln?Val?Tyr?Phe?Gly

165?????????????????170?????????????????175Ile?Ile?Ala?Leu

180

<210>9

<21l>801

<212>DNA

＜213〉artificial sequence

<220>

＜223〉fusion constructs

<221>CDS

<222>(1)...(798)

<400>9atg?aaa?aag?aca?gct?atc?gcg?att?gca?gtg?gca?ctg?gct?ggt?ttc?gct???????48Met?Lys?Lys?Thr?Ala?Ile?Ala?Ile?Ala?Val?Ala?Leu?Ala?Gly?Phe?Ala?1???????????????5???????????????????10??????????????????15acc?gta?gcg?cag?gcc?cat?atg?gct?aac?gag?ctg?aag?cag?atg?cag?gac???????96Thr?Val?Ala?Gln?Ala?His?Met?Ala?Asn?Glu?Leu?Lys?Gln?Met?Gln?Asp

20??????????????????25??????????????????30aag?tac?tcc?aaa?agt?ggc?att?gct?tgt?ttc?tta?aaa?gaa?gat?gac?agt??????144Lys?Tyr?Ser?Lys?Ser?Gly?Ile?Ala?Cys?Phe?Leu?Lys?Glu?Asp?Asp?Ser

35??????????????????40??????????????????45tat?tgg?gac?ccc?aat?gac?gaa?gag?agt?atg?aac?agc?ccc?tgc?tgg?caa??????192Tyr?Trp?Asp?Pro?Asn?Asp?Glu?Glu?Ser?Met?Asn?Ser?Pro?Cys?Trp?Gln

50??????????????????55??????????????????60gtc?aag?tgg?caa?ctc?cgt?cag?ctc?gtt?aga?aag?atg?att?ttg?aga?acc??????240Val?Lys?Trp?Gln?Leu?Arg?Gln?Leu?Val?Arg?Lys?Met?Ile?Leu?Arg?Thr?65??????????????????70??????????????????75??????????????????80tct?gag?gaa?acc?att?tct?aca?gtt?caa?gaa?aag?caa?caa?aat?att?tct??????288Ser?Glu?Glu?Thr?Ile?Ser?Thr?Val?Gln?Glu?Lys?Gln?Gln?Asn?Ile?Ser

85??????????????????90??????????????????95ccc?cta?gtg?aga?gaa?aga?ggt?cct?cag?aga?gta?gca?gct?cac?ata?act??????336Pro?Leu?Val?Arg?Glu?Arg?Gly?Pro?Gln?Arg?Val?Ala?Ala?His?Ile?Thr

100?????????????????105?????????????????110ggg?acc?aga?gga?aga?agc?aac?aca?ttg?tct?tct?cca?aac?tcc?aag?aat??????384Gly?Thr?Arg?Gly?Arg?Ser?Asn?Thr?Leu?Ser?Ser?Pro?Asn?Ser?Lys?Asn

115?????????????????120?????????????????125gaa?aag?gct?ctg?ggc?cgc?aaa?ata?aac?tcc?tgg?gaa?tca?tca?agg?agt??????432Glu?Lys?Ala?Leu?Gly?Arg?Lys?Ile?Asn?Ser?Trp?Glu?Ser?Ser?Arg?Set

130?????????????????135?????????????????140ggg?cat?tca?ttc?ctg?agc?aac?ttg?cac?ttg?agg?aat?ggt?gaa?ctg?gtc??????480Gly?His?Ser?Phe?Leu?Ser?Asn?Leu?His?Leu?Arg?Asn?Gly?Glu?Leu?Val145?????????????????150?????????????????155?????????????????160atc?cat?gaa?aaa?ggg?ttt?tac?tac?atc?tat?tcc?caa?aca?tac?ttt?cga??????528Ile?His?Glu?Lys?Gly?Phe?Tyr?Tyr?Ile?Tyr?Ser?Gln?Thr?Tyr?Phe?Arg

165?????????????????170?????????????????175ttt?cag?gag?gaa?ata?aaa?gaa?aac?aca?aag?aac?gac?aaa?caa?atg?gtc??????576Phe?Gln?Glu?Glu?Ile?Lys?Glu?Asn?Thr?Lys?Asn?Asp?Lys?Gln?Met?Val

180?????????????????185?????????????????190caa?tat?att?tac?aaa?tac?aca?agt?tat?cct?gac?cct?ata?ttg?ttg?atg??????624Gln?Tyr?Ile?Tyr?Lys?Tyr?Thr?Ser?Tyr?Pro?Asp?Pro?Ile?Leu?Leu?Met

195?????????????????200?????????????????205aaa?agt?gct?aga?aat?agt?tgt?tgg?tct?aaa?gat?gca?gaa?tat?gga?ctc??????672Lys?Ser?Ala?Arg?Asn?Ser?Cys?Trp?Ser?Lys?Asp?Ala?Glu?Tyr?Gly?Leu

210?????????????????215?????????????????220tat?tcc?atc?tat?caa?ggg?gga?ata?ttt?gag?ctt?aag?gaa?aat?gac?aga??????720Tyr?Ser?Ile?Tyr?Gln?Gly?Gly?Ile?Phe?Glu?Leu?Lys?Glu?Asn?Asp?Arg225?????????????????230?????????????????235?????????????????240att?ttt?gtt?tct?gta?aca?aat?gag?cac?ttg?ata?gac?atg?gac?cat?gaa??????768Ile?Phe?Val?Ser?Val?Thr?Asn?Glu?His?Leu?Ile?Asp?Met?Asp?His?Glu

245?????????????????250?????????????????255gcc?agt?ttt?ttc?ggg?gcc?ttt?tta?gtt?ggc?taa??????????????????????????801Ala?Ser?Phe?Phe?Gly?Ala?Phe?Leu?Val?Gly

260?????????????????265

<210>10

<211>266

<212>?PRT

＜213〉artificial sequence

<400>10Met?Lys?Lys?Thr?Ala?Ile?Ala?Ile?Ala?Val?Ala?Leu?Ala?Gly?Phe?Ala?1???????????????5??????????????????10??????????????????15Thr?Val?Ala?Gln?Ala?His?Met?Ala?Asn?Glu?Leu?Lys?Gln?Met?Gln?Asp

20??????????????????25??????????????????30Lys?Tyr?Ser?Lys?Ser?Gly?Ile?Ala?Cys?Phe?Leu?Lys?Glu?Asp?Asp?Ser

35??????????????????40??????????????????45Tyr?Trp?Asp?Pro?Asn?Asp?Glu?Glu?Ser?Met?Asn?Ser?Pro?Cys?Trp?Gln

50??????????????????55??????????????????60Val?Lys?Trp?Gln?Leu?Arg?Gln?Leu?Val?Arg?Lys?Met?Ile?Leu?Arg?Thr65??????????????????70??????????????????75??????????????????80Ser?Glu?Glu?Thr?Ile?Ser?Thr?Val?Gln?Glu?Lys?Gln?Gln?Asn?Ile?Ser

85??????????????????90??????????????????95Pro?Leu?Val?Arg?Glu?Arg?Gly?Pro?Gln?Arg?Val?Ala?Ala?His?Ile?Thr

100?????????????????105?????????????????110Gly?Thr?Arg?Gly?Arg?Ser?Asn?Thr?Leu?Ser?Ser?Pro?Asn?Ser?Lys?Asn

115?????????????????120?????????????????125Glu?Lys?Ala?Leu?Gly?Arg?Lys?Ile?Asn?Ser?Trp?Glu?Ser?Ser?Arg?Ser

130?????????????????135?????????????????140Gly?His?Ser?Phe?Leu?Ser?Asn?Leu?His?Leu?Arg?Asn?Gly?Glu?Leu?Val145?????????????????150?????????????????155?????????????????160Ile?His?Glu?Lys?Gly?Phe?Tyr?Tyr?Ile?Tyr?Ser?Gln?Thr?Tyr?Phe?Arg

165?????????????????170?????????????????175Phe?Gln?Glu?Glu?Ile?Lys?Glu?Asn?Thr?Lys?Asn?Asp?Lys?Gln?Met?Val

180?????????????????185?????????????????190Gln?Tyr?Ile?Tyr?Lys?Tyr?Thr?Ser?Tyr?Pro?Asp?Pro?Ile?Leu?Leu?Met

195?????????????????200?????????????????205Lys?Ser?Ala?Arg?Asn?Ser?Cys?Trp?Ser?Lys?Asp?Ala?Glu?Tyr?Gly?Leu

210?????????????????215?????????????????220Tyr?Ser?Ile?Tyr?Gln?Gly?Gly?Ile?Phe?Glu?Leu?Lys?Glu?Asn?Asp?Arg225?????????????????230?????????????????235?????????????????240Ile?Phe?Val?Ser?Val?Thr?Asn?Glu?His?Leu?Ile?Asp?Met?Asp?His?Glu

245?????????????????250?????????????????255Ala?Ser?Phe?Phe?Gly?Ala?Phe?Leu?Val?Gly

260?????????????????265

<210>11

<211>465

<212>DNA

＜213〉artificial sequence

<220>

＜223〉fusion constructs

<221>CDS

<222>(1)...(462)

<400>11atg?aaa?aag?acg?gct?ctg?gcg?ctt?ctg?ctc?ttg?ctg?tta?gcg?ctg?act???????48Met?Lys?Lys?Thr?Ala?Leu?Ala?Leu?Leu?Leu?Leu?Leu?Leu?Ala?Leu?Thr?1???????????????5???????????????????10??????????????????15agt?gta?gcg?cag?gcc?gct?cct?act?agc?tcg?agc?act?aag?aaa?act?caa???????96Ser?Val?Ala?Gln?Ala?Ala?Pro?Thr?Ser?Ser?Ser?Thr?Lys?Lys?Thr?Gln

20??????????????????25??????????????????30ctg?caa?ttg?gag?cat?ctg?ctg?ctg?gat?ctg?cag?atg?att?ctg?aat?ggc??????144Leu?Gln?Leu?Glu?His?Leu?Leu?Leu?Asp?Leu?Gln?Met?Ile?Leu?Asn?Gly

35??????????????????40??????????????????45atc?aat?aac?tac?aag?aac?cct?aag?ctg?act?cgc?atg?ctg?act?ttc?aaa??????192Ile?Asn?Asn?Tyr?Lys?Asn?Pro?Lys?Leu?Thr?Arg?Met?Leu?Thr?Phe?Lys

50??????????????????55??????????????????60ttc?tac?atg?ccg?aaa?aag?gct?acc?gag?ctc?aaa?cat?ctc?cag?tgc?ctg??????240Phe?Tyr?Met?Pro?Lys?Lys?Ala?Thr?Glu?Leu?Lys?His?Leu?Gln?Cys?Leu?65??????????????????70??????????????????75??????????????????80gaa?gag?gaa?ctg?aag?ccg?ctg?gag?gaa?gta?ctt?aac?ctg?gca?cag?tct??????288Glu?Glu?Glu?Leu?Lys?Pro?Leu?Glu?Glu?Val?Leu?Asn?Leu?Ala?Gln?Ser

85??????????????????90??????????????????95aag?aac?ttc?cac?ctg?cgt?ccg?cgt?gac?ctg?atc?tcc?aac?atc?aat?gta??????336Lys?Asn?Phe?His?Leu?Arg?Pro?Arg?Asp?Leu?Ile?Ser?Asn?Ile?Asn?Val

100?????????????????105?????????????????110atc?gtt?ctt?gag?ctg?aag?gga?tcc?gaa?acc?acc?ttc?atg?tgc?gaa?tac??????384Ile?Val?Leu?Glu?Leu?Lys?Gly?Ser?Glu?Thr?Thr?Phe?Met?Cys?Glu?Tyr

115?????????????????120?????????????????125gct?gac?gaa?acc?gcc?acc?att?gtg?gag?ttc?ctg?aac?cgt?tgg?atc?acc??????432Ala?Asp?Glu?Thr?Ala?Thr?Ile?Val?Glu?Phe?Leu?Asn?Arg?Trp?Ile?Thr

130?????????????????135?????????????????140ttt?gcc?caa?tcg?atc?att?agc?acg?tta?act?taa??????????????????????????465Phe?Ala?Gln?Ser?Ile?Ile?Ser?Thr?Leu?Thr145?????????????????150

<210>12

<211>154

<212>PRT

＜213〉artificial sequence

<400>12Met?Lys?Lys?Thr?Ala?Leu?Ala?Leu?Leu?Leu?Leu?Leu?Leu?Ala?Leu?Thr?1???????????????5??????????????????10??????????????????15Ser?Val?Ala?Gln?Ala?Ala?Pro?Thr?Ser?Ser?Ser?Thr?Lys?Lys?Thr?Gln

20??????????????????25??????????????????30Leu?Gln?Leu?Glu?His?Leu?Leu?Leu?Asp?Leu?Gln?Met?Ile?Leu?Asn?Gly

35??????????????????40??????????????????45Ile?Asn?Asn?Tyr?Lys?Asn?Pro?Lys?Leu?Thr?Arg?Met?Leu?Thr?Phe?Lys

50??????????????????55??????????????????60Phe?Tyr?Met?Pro?Lys?Lys?Ala?Thr?Glu?Leu?Lys?His?Leu?Gln?Cys?Leu65??????????????????70??????????????????75??????????????????80Glu?Glu?Glu?Leu?Lys?Pro?Leu?Glu?Glu?Val?Leu?Asn?Leu?Ala?Gln?Ser

85??????????????????90??????????????????95Lys?Asn?Phe?His?Leu?Arg?Pro?Arg?Asp?Leu?Ile?Ser?Asn?Ile?Asn?Val

100?????????????????105?????????????????110Ile?Val?Leu?Glu?Leu?Lys?Gly?Ser?Glu?Thr?Thr?Phe?Met?Cys?Glu?Tyr

115?????????????????120?????????????????125Ala?Asp?Glu?Thr?Ala?Thr?Ile?Val?Glu?Phe?Leu?Asn?Arg?Trp?Ile?Thr

130?????????????????135?????????????????140Phe?Ala?Gln?Ser?Ile?Ile?Ser?Thr?Leu?Thr145?????????????????150

<210>13

<211>465

<212>DNA

＜213〉artificial sequence

<220>

＜223〉fusion constructs

<221>CDS

<222>(1)...(462)

<400>13atg?aaa?cag?tcg?act?ctg?gcg?ctt?ctg?ctc?ttg?ctg?tta?gcg?ctg?act???????48Met?Lys?Gln?Ser?Thr?Leu?Ala?Leu?Leu?Leu?Leu?Leu?Leu?Ala?Leu?Thr?1???????????????5???????????????????10??????????????????15agt?gtg?gcc?aaa?gcg?gct?cct?act?agc?tcg?agc?act?aag?aaa?act?caa???????96Ser?Val?Ala?Lys?Ala?Ala?Pro?Thr?Ser?Ser?Ser?Thr?Lys?Lys?Thr?Gln

<210>14

<211>154

<212>PRT

＜213〉artificial sequence

<400>14Met?Lys?Gln?Ser?Thr?Leu?Ala?Leu?Leu?Leu?Leu?Leu?Leu?Ala?Leu?Thr?1???????????????5??????????????????10??????????????????15Ser?Val?Ala?Lys?Ala?Ala?Pro?Thr?Ser?Ser?Ser?Thr?Lys?Lys?Thr?Gln

130?????????????????135?????????????????140Phe?Ala?G1n?Ser?Ile?Ile?Ser?Thr?Leu?Thr145?????????????????150

<210>15

<211>26

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>15agtctagaca?atcaggcgaa?gaacgg????????????????????????????????????????????26

<210>16

<211>25

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>16agccatggag?tcaccctcac?ttttc?????????????????????????????????????????????25

<210>17

<211>31

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>17ggatccttaa?gacccacttt?cacatttaag?t??????????????????????????????????????31

<210>18

<211>28

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>18ggttccatgg?ttcacttttc?tctatcac?????????????????????????????????????????28

<210>19

<211>33

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>19gtgtccatgg?ggcacagcca?ccgcgacttc?cag???????????????????????????????????33

<210>20

<211>34

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>20acacgagctc?ctacttggag?gcagtcatga?agct??????????????????????????????????34

<210>21

<211>72

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>21gtgtccatgg?ctcggcgggc?aagtgtcggg?actgaccatc?atcatcatca?tcatcacagc??????60caccgcgact?tc??????????????????????????????????????????????????????????72

<210>22

<211>35

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>22gtgcggatcc?ctacttggag?gcagtcatga?agctg???????????????????????????????????35

<210>23

<211>16

<212>PRT

＜213〉people (Homo sapiens)

<400>23Met?Ala?Arg?Arg?Ala?Ser?Val?Gly?Thr?Asp?His?His?His?His?His?His?1???????????????5??????????????????10??????????????????15

<210>24

<211>22

<212>PRT

＜213〉artificial sequence

<220>

＜223〉peptide sequence of Tip 13.40

<400>24Ala?Tyr?Arg?Trp?Arg?Leu?Ser?His?Arg?Pro?Lys?Thr?Gly?Phe?Ile?Arg?1???????????????5??????????????????10??????????????????15Val?Val?Met?Tyr?Glu?Gly

20

<210>25

<211>66

<212>DNA

＜213〉artificial sequence

<220>

＜223〉nucleotide sequence of coding Tip 13.40

<400>25gcgtaccgct?ggcgcctgtc?ccatcgcccg?aaaaccggct?ttatccgcgt?ggtgatgtac??????60gaaggc?????????????????????????????????????????????????????????????????66

<210>26

<211>101

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>26gtgtactagt?gtggcgcagg?cggcgtaccg?ctggcgcctg?tcccatcgcc?cgaaaaccgg??????60ctttatccgc?gtggtgatgt?acgaaggcta?aggatccgcg?c?????????????????????????101

<210>27

<211>101

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>27gcgcggatcc?ttagccttcg?tacatcacca?cgcggataaa?gccggttttc?gggcgatggg??????60acaggcgcca?gcggtacgcc?gcctgcgcca?cactagtaca?c?????????????????????????101

<210>28

<211>101

<212>PRT

＜213〉people (Homo sapiens)

<400>28Met?Ser?Ser?Ala?Ala?Gly?Phe?Cys?Ala?Ser?Arg?Pro?Gly?Leu?Leu?Phe?1???????????????5??????????????????10??????????????????15Leu?Gly?Leu?Leu?Leu?Leu?Pro?Leu?Val?Val?Ala?Phe?Ala?Ser?Ala?Glu

20??????????????????25??????????????????30Ala?Glu?Glu?Asp?Gly?Asp?Leu?Gln?Cys?Leu?Cys?Val?Lys?Thr?Thr?Ser

35??????????????????40??????????????????45Gln?Val?Arg?Pro?Arg?His?Ile?Thr?Ser?Leu?Glu?Val?Ile?Lys?Ala?Gly

50??????????????????55??????????????????60Pro?His?Cys?Pro?Thr?Ala?Gln?Leu?Ile?Ala?Thr?Leu?Lys?Asn?Gly?Arg65??????????????????70??????????????????75??????????????????80Lys?Ile?Cys?Leu?Asp?Leu?Gln?Ala?Pro?Leu?Tyr?Lys?Lys?Ile?Ile?Lys

85??????????????????90??????????????????95Lys?Leu?Leu?Glu?Ser

100

<210>29

<211>106

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>29cttcactagt?gtggcgcagg?cgaacggccg?caaaatctgc?ctggacctgc?aggcgccgct??????60gtacaaaaaa?atcatcaaaa?aactgctgga?aagctaagga?tccgcg????????????????????106

<210>30

<211>106

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>30cgcggatcct?tagctttcca?gcagtttttt?gatgattttt?ttgtacagcg?gcgcctgcag??????60gtccaggcag?attttgcggc?cgttcgcctg?cgccacacta?gtgaag????????????????????106

<210>31

<211>85

<212>PRT

＜213〉people (Homo sapiens)

<400>31Ile?Tyr?Ser?Phe?Asp?Gly?Arg?Asp?Ile?Met?Thr?Asp?Pro?Ser?Trp?Pro??1??????????????5??????????????????10??????????????????15Gln?Lys?Val?Ile?Trp?His?Gly?Ser?Ser?Pro?His?Gly?Val?Arg?Leu?Val

20??????????????????25??????????????????30Asp?Asn?Tyr?Cys?Glu?Ala?Trp?Arg?Thr?Ala?Asp?Thr?Ala?Val?Thr?Gly

35??????????????????40??????????????????45Leu?Ala?Ser?Pro?Leu?Ser?Thr?Gly?Lys?Ile?Leu?Asp?Gln?Lys?Ala?Tyr

50??????????????????55??????????????????60Ser?Cys?Ala?Asn?Arg?Leu?Ile?Val?Leu?Cys?Ile?Glu?Asn?Ser?Phe?Met65??????????????????70??????????????????75??????????????????80Thr?Asp?Ala?Arg?Lys

85

<210>32

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>32ggcttcacta?gtgtggcgca?ggcgatatac?tcctttgatg?gtcg???????????????????????44

<210>33

<211>37

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>33cgcggatcct?tacttcctag?cgtctgtcat?gaaactg???????????????????????????????37

<210>34

<211>7117

<212>DNA

＜213〉escherichia coli (E.Coli)

<400>34cccgggcact?tccggggcat?gagtatgtga?tatccggggc?tgcaccccgg?accccgccaa??????60cacatcacgg?gccacaaaat?tttttgtggc?ccgctctgcg?ttttctaagt?gttatccctc?????120ctgatttcta?aaaaattttc?cacctgaact?tgacagaaaa?aacgatgacg?agtacttttt?????180gatctgtaca?taaacccagt?ggttttatgt?acagtattaa?tcgtgtaatc?aattgtttta?????240acgcttaaaa?gagggaattt?ttatgagcgg?tggcgatgga?cgcggccata?acacgggcgc?????300gcatagcaca?agtggtaaca?ttaatggtgg?cccgaccggg?cttggtgtag?gtggtggtgc?????360ttctgatggc?tccggatgga?gttcggaaaa?taacccgtgg?ggtggtggtt?ccggtagcgg?????420cattcactgg?ggtggtggtt?ccggtcatgg?taatggcggg?gggaatggta?attccggtgg?????480tggttcggga?acaggcggta?atctgtcagc?agtagctgcg?ccagtggcat?ttggttttcc?????540ggcactttcc?actccaggag?ctggcggtct?ggcggtcagt?atttcagcgg?gagcattatc?????600ggcagctatt?gctgatatta?tggctgccct?gaaaggaccg?tttaaatttg?gtctttgggg?????660ggtggcttta?tatggtgtat?tgccatcaca?aatagcgaaa?gatgacccca?atatgatgtc?????720aaagattgtg?acgtcattac?ccgcagatga?tattactgaa?tcacctgtca?gttcattacc?????780tctcgataag?gcaacagtaa?acgtaaatgt?tcgtgttgtt?gatgatgtaa?aagacgagcg?????840acagaatatt?tcggttgttt?caggtgttcc?gatgagtgtt?ccggtggttg?atgcaaaacc?????900taccgaacgt?ccgggtgttt?ttacggcatc?aattccaggt?gcacctgttc?tgaatatttc?????960agttaataac?agtacgccag?cagtacagac?attaagccca?ggtgttacaa?ataatactga????1020taaggatgtt?cgcccggcag?gatttactca?gggtggtaat?accagggatg?cagttattcg????1080attcccgaag?gacagcggtc?ataatgccgt?atatgtttca?gtgagtgatg?ttcttagccc????1140tgaccaggta?aaacaacgtc?aagatgaaga?aaatcgccgt?cagcaggaat?gggatgctac????1200gcatccggtt?gaagcggctg?agcgaaatta?tgaacgcgcg?cgtgcagagc?tgaatcaggc????1260aaatgaagat?gttgccagaa?atcaggagcg?acaggctaaa?gctgttcagg?tttataattc????1320gcgtaaaagc?gaacttgatg?cagcgaataa?aactcttgct?gatgcaatag?ctgaaataaa????1380acaatttaat?cgatttgccc?atgacccaat?ggctggcggt?cacagaatgt?ggcaaatggc????1440cgggcttaaa?gcccagcggg?cgcagacgga?tgtaaataat?aagcaggctg?catttgatgc????1500tgctgcaaaa?gagaagtcag?atgctgatgc?tgcattgagt?tctgctatgg?aaagcaggaa????1560gaagaaagaa?gataagaaaa?ggagtgctga?aaataattta?aacgatgaaa?agaataagcc????1620cagaaaaggt?tttaaagatt?acgggcatga?ttatcatcca?gctccgaaaa?ctgagaatat????1680taaagggctt?ggtgatctta?agcctgggat?accaaaaaca?ccaaagcaga?atggtggtgg????1740aaaacgcaag?cgctggactg?gagataaagg?gcgtaagatt?tatgagtggg?attctcagca????1800tggtgagctt?gaggggtatc?gtgccagtga?tggtcagcat?cttggctcat?ttgaccctaa????1860aacaggcaat?cagttgaaag?gtccagatcc?gaaacgaaat?atcaagaaat?atctttgaga????1920ggaagttatg?ggacttaaat?tggatttaac?ttggtttgat?aaaagtacag?aagattttaa????1980gggtgaggag?tattcaaaag?attttggaga?tgacggttca?gttatggaaa?gtctaggtgt????2040gccttttaag?gataatgtta?ataacggttg?ctttgatgtt?atagctgaat?gggtaccttt????2100gctacaacca?tactttaatc?atcaaattga?tatttccgat?aatgagtatt?ttgtttcgtt????2160tgattatcgt?gatggtgatt?ggtgatcaaa?tattatcagg?gatgagttga?tatacgggct????2220tctagtgttc?atggatgaac?gctggagcct?ccaaatgtag?aaatgttata?ttttttattg????2280agttcttggt?tataattgct?ccgcaatgat?ttaaataagc?attatttaaa?acattctcag????2340gagaggtgaa?ggtggagcta?aaaaaaagta?ttggtgatta?cactgaaacc?gaattcaaaa????2400aatttattga?agacatcatc?aattgtgaag?gtgatgaaaa?aaaacaggat?gataacctcg????2460agtattttat?aaatgttact?gagcatccta?gtggttctga?tctgatttat?tacccagaag????2520gtaataatga?tggtagccct?gaaggtgtta?ttaaagagat?taaagaatgg?cgagccgcta????2580acggtaagtc?aggatttaaa?cagggctgaa?atatgaatgc?cggttgttta?tggatgaatg????2640gctggcattc?tttcacaaca?aggagtcgtt?atgaaaaaaa?taacagggat?tattttattg????2700cttcttgcag?tcattattct?gtctgcatgt?caggcaaact?atatccggga?tgttcagggc????2760gggaccgtat?ctccgtcatc?aacagctgaa?gtgaccggat?tagcaacgca?gtaacccgaa????2820atcctctttg?acaaaaacaa?agcgtgtcag?gctgattctg?atgcgctttt?tttttgaaat?????2880gtcacaaaaa?ttccatgtgg?gagatgggat?ctaaaatcct?cgtgcagaac?tttccatcca?????2940gggggagaaa?acttgtcgtt?ttgagccgtt?cggtgttcag?aacgcacgaa?accgatcgcg?????3000cgcatcgctt?tcgtgaatag?ttatgcaggc?ccctgaaaac?gattctgacg?cgttttttcg?????3060gttttgcctg?gtgttttcct?gtctttttgc?gttttttgcg?tcagaacgcg?tctgagggcg?????3120ttttaagggg?tgcgtacaac?gggagttatg?gtaaatggat?cggtttttcg?ggaaggatcg?????3180acaggatttg?ccgttgggtg?tagtgtaagc?gactgaaaaa?caaacgcccc?gtaaatcgtg?????3240ctctcaccgc?caagattgat?cacgaaatta?cagggcgccg?ggttccgcgt?ttcccgatgg?????3300gaaagcgcgg?ttagttaaac?tgtgtaccga?gagaaatcgt?atcacatgag?cgccgtactt?????3360caacgcttca?gggaaaaatt?accgcacaaa?ccgtactgta?cgaacgattt?cgcgtacggc?????3420gttcgcattc?tgccgaaaaa?cattgccatt?cttgcccgtt?tcatccagca?gaaccagcca?????3480catgcactgt?actggcttcc?ctttgacgtg?gaccggacgg?gggcatcaat?cgactggagc?????3540gaccggaatt?gtccggcccc?gaacatcacc?gtaaaaaatc?cccgtaacgg?gcacgcgcat?????3600ctgctctacg?cgctcgccct?tcctgtgaga?actgcgccgg?atgcatcggc?ttcggcgctc?????3660agatacgctg?ccgctattga?gcgtgcgttg?tgtgaaaaac?tgggcgcgga?tgtgaattac?????3720agcggcctga?tctgcaaaaa?tccgtgccac?cctgaatggc?aggaagtgga?atggcgcgag?????3780gaaccctaca?ctctcgacga?actggctgat?tatctcgatt?tgagcgcctc?agcgcgccgt?????3840agcgtcgata?aaaattacgg?gctggggcga?aactgctatc?tgttcgaaaa?gggccgtaaa?????3900tgggcttacc?gggctattcg?tcagggctgg?ccggcattct?cacaatggct?tgatgcggtg?????3960attcagcgtg?tcgaaatgta?caacgcatcg?ctccccgttc?cgctttcacc?tcctgaatgt?????4020cgggctattg?gcaagagtat?tgcgaaatac?acgcacagga?acttcacgcc?ggaaactttc?????4080gcacagtatg?tggctgatac?gcacacgcca?gaaattcagg?ctacacgcgg?tcgcaagggc?????4140ggttctaagt?ctaagcgcgg?cacagtagct?acatcagcac?gcacgctgaa?accttgggag?????4200aaattaggga?tcagtcgcgc?ctggtattac?caactgaaaa?aacgaggtct?cgtagagtag?????4260accaaataag?cctatatcag?ataacagcgc?ctttttggcg?cctttttgag?cagcttggtt?????4320tgttgctatt?tccctcgttg?aatcccgcaa?tggcgcggct?ttccgcatga?ttgaggtggt?????4380agcgctcgcc?gcagtctcat?gaccgagcgt?agcgagcgaa?tgagcgagga?agcgcaaagg?????4440cgtccggtgg?tgcatgtggc?acttacgcgc?cggggcttag?tggttctgcg?gtttcgccgg?????4500tggtctgggt?agcttctcca?gctcgttaat?cagcggttgt?agtcggttca?catccacctg?????4560tcttgtgact?tcctttcgca?gaaactggag?caggaacgca?cgcagttgcg?cttcttccgg?????4620cctccgtacc?cttgccagca?tggctgcccc?cacaatgact?ttttgcgccg?tgtccaggct?????4680tcggctcttc?gccttcaggc?gctgtaatct?ggcctcagct?tcggcaatct?tctgttcgag?????4740tgttctgctc?atttcgtgac?tccgtgcgcg?gtgaaaaatc?gcattttagc?gcgtcactgg?????4800tagtttaaaa?actaaactgg?cataatgcac?ggcacatcac?gaagtgcgca?cttatacaat?????4860ctccacttcg?tttcgattgt?gtgcggtctg?cgacgctaaa?agaaaacggc?aaaaaggcat?????4920tacggcagaa?atggcgattt?atcatctcag?catgaaaatc?atttcgcgaa?aaaacggcta?????4980cagtgctgtt?gcttctgctg?cctaccgttc?cggctctgtc?atacccgatg?accgtaccgg?????5040attaatccac?gattacaccc?gtaaacgcgg?cgttgatgat?gcggtcattc?tcacccctgc?????5100gaatgcaccg?tcctggtgtg?ttgaccgttc?cgttctttgg?aatgcggtcg?agaaagccga?????5160acagcgccgg?aactcccagc?tggcaaggga?ggttgaactc?gccattcccc?gtgagatttc?????5220ccgcgaggcc?gcacgggaga?ccgttctcgc?tttgtccggg?aaaactttgt?cagtcggggc?????5280atgattgccg?atgtggcgtt?ccatcacatg?gaccggacca?atccccatgc?gcacatcatg?????5340ctgaccacga?gagctgtcgg?ggaaacggga?ttcgcaggaa?aggtcaggga?tggaacgacc?????5400gggcactcgc?cgagacgtgg?cgcgcatcat?gggctgacca?tgcgaacaga?gcgcttgcga?????5460acgccggcta?ccaggaagag?atagaccatc?gttcatacga?gcgtcaggga?ctggagaaag?????5520cgccggcctt?cacctcggaa?aggctgcctg?tgcgatggaa?aaacggggaa?tggaaacaga?????5580acgcggtgag?cagaaccgtc?tgattaacag?ccttaacctg?gaaatacagg?tttcccgcac?????5640gcagcttgct?ctcaggacgg?ttcaggaaac?gcagcgtaag?cgggaactca?gcgatgctgc?????5700acgtcgtgca?gtggaagccc?ttaacctgac?cattcccgct?gcgaatgcct?cagcggatac?????5760cctgcgggaa?ttcattgcca?cgctgccgca?ggaatgcggg?aacgcgtggg?agatgacccc?????5820ggagttcctg?gcgatgagcg?ggaaggtgaa?cgacatcgaa?cgtgagggga?atgcgctgct?????5880gaaagagcag?gccattctcg?aaaaggagat?gaccggactc?aaaaaagcac?gccctgtcgc?????5940gtcccttctg?tcagagattc?ccctgatgac?atgggctgaa?ccggaatacc?gcaaaagaca?????6000actccgtttc?ttggaaactc?gggaaacaga?ttgaatctct?tcgccgcacc?tacagggccg?????6060tgaaagaacg?ggacattccc?gcccgtcgtc?aggcctttga?aacgcagtgg?aatacgtgga?????6120ttgcgccgga?atggcagagc?tgaaagaaaa?actgtcagca?cgggaagcgg?agcggcgcag?????6180ggaggagccc?gaagcggaag?cgcgccggaa?ggaacaggag?catgaggcgc?ggctgaaacg?????6240tcatgataac?caccgtctga?gccgtgaaac?ggcattagtc?ggggttatta?cggagctggg?????6300gcgtgccaga?gagccgggaa?cgggcaggat?aacccgctac?atgatgttga?gtaacagagc?????6360cggagaattc?acggtatggg?gtgatgagct?ggcgcattac?ccccagagtg?ttcatgaccc?????6420ggtgaatgtt?tacctgtcgc?caggcggggc?tgtgatggtc?tcggatatac?gtgagggaat?????6480gccagaatct?catgagacga?tggcgcggcc?tgagcgtgtg?agaatgtatt?ccggtgcgac?????6540ggtccggcat?gtactggaac?agatgcgcca?ggggtggccc?tcttacggtt?ttccggcgct?????6600gccgcatcac?tggccggata?atttttattt?cagcgacgac?cgcaggcccg?tagcctctcc?????6660gctgccgtct?gcgcaccggg?tggacgtcac?cgcttatgcg?gcaccggagc?aactcatgcc?????6720cgttgtattt?tcgacagagc?gaaacagcag?gacgctgaat?ctgctgttgt?gcaaagggcc?????6780ggaggaagtg?cttgtcggat?ttgtgcgcca?ggaggacggg?ctgcgtcccg?ttcttgcgct?????6840tccgtcgccg?gattacagtc?atctgatggt?cagcaccatc?acggagaacg?gggtatgcct?????6900ggcaggttac?ggagaagcta?taaaccatga?tgcggatact?ccgtacccac?cggaaccgca?????6960cctgatgcag?ttccggctca?aaggccatca?tgacaggctt?ttggctgctg?tccacaaacc?????7020ggaagagatg?ccggattatc?tcttccgtca?actcggtttt?aatcagacct?ggcatgagtg?????7080gaagcgggac?gaacagcaca?ggcaacaaca?acgccgc??????????????????????????????7117

<210>35

<211>30

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>35gtgtcatgaa?aatgggtaac?caatggcaac?????????????????????????????????????30

<210>36

<211>35

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>36cacagagctc?gcgctaacaa?aacagcacaa?gggag??????????????????????????????35

<210>37

<211>37

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>37gtgtccatgg?ctaaaacatt?attaatagct?gcatcgc????????????????????????????37

<210>38

<211>29

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>38gtgtctgcag?aactgactga?attgagatg??????????????????????????????????????29

<210>39

<211>37

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>39gtgtagatct?ttaagaccca?ctttcacatt?taagttg?????????????????????????????37

<210>40

<211>30

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>40cacaggatcc?ttactgaacc?gcgatccccg?????????????????????????????????????30

<210>41

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>41gtgtgagctc?gatcaaccag?caagccgtta?accctctgac??????????????????????????40

<210>42

<211>67

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>42gtgtgcatgc?ggggggccat?ataggccggg?gatttaaatg?caaacgtccg?ccgaaacgcc????60gacgcac??????????????????????????????????????????????????????????????67

<210>43

<211>71

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>43gtgtgcatgc?ggggttaatt?aagggggcgg?ccgcgtggta?ttggttgaac?cgacggtgct??????60catgacatcg?c?????????????????????????????????????????????????????????71

<210>44

<211>37

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>44gtgtctcgag?gatatcattc?tggcctctga?cgttgtg?????????????????????????????37

<210>45

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>45ttttttccat?ggctattatg?actgaaatcg?ttgcagataa?aacgg??????????????????????45

<210>46

<211>46

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>46ttttttaagc?ttcccgggtc?agacttcagg?tacctcaaag?agtgtc?????????????????????46

<210>47

<211>33

<212>DNA

＜213〉artificial sequence

<220>

＜223〉forward primer

<400>47ccgctcgaga?tgcacggctc?caacaagctc?cca???????????????????????????????????33

<210>48

<211>33

<212>DNA

＜213〉artificial sequence

<220>

＜223〉reverse primer

<400>48cgcggatcct?taggcactcg?ccttgagtgc?ctg??????????????????????????????????33

<210>49

<211>102

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>49gatcccatgg?cttatggcag?aaaaaaacgc?cgtcagcgcc?gtcgcatgaa?cgcgctgcag??????60gaagataccc?cgccgggccc?gtccaccgtg?tttcgcccgc?cg????????????????????????102

<210>50

<211>103

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>50gggacagggt?gatggtgatg?cccgcgatgc?cgatgcggat?ttcgcggcaa?tgcggggttt??????60ccagcgggcg?ggaggaggtc?ggcgggcgaa?acacggtgga?cgg???????????????????????103

<210>51

<211>102

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>51ggcatcgcgg?gcatcaccat?caccctgtcc?ctgtgcggct?gcgcgaacgc?gcgcgcgccg??????60accctgcgct?ccgcgaccgc?ggataactcc?gaaaacaccg?gc????????????????????????102

<210>52

<211>111

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>52gcgatattcg?gacggatcgc?aggagcgttt?tttggacggc?ggtttcggct?gatcggtgcg??????60cagatccggg?acgtttttaa?agccggtgtt?ttcggagtta?tccgcggtcg?c??????????????111

<210>53

<211>111

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>53cctgcgatcc?gtccgaatat?cgcgtctccg?aactgaaaga?atccctgatc?accaccaccc??????60cgtcccgccc?gcgcaccgcc?cgccgctgca?tccgcctctg?aaagcttcat?g??????????????111

<210>54

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>54catgaagctt?tcagaggcgg?atgcagcggc?gggcggtgcg?c???????????????????????????41

<210>55

<211>98

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>55gatcccatgg?ctcatcacca?tcaccaccat?tatggccgca?aaaaacgccg?tcagcgccgt??????60cgcatgaacg?cgctgcagga?agataccccg?ccgggccc??????????????????????????????98

<210>56

<211>100

<212>DNA

＜213〉artificial sequence

<220>

＜223〉oligonucleotide

<400>56gatcccatgg?ctaaaaagac?ggctctggcg?cttctgctct?tgctgttagc?gctgactagt??????60gtagcgcagg?cctatggccg?caaaaaacgc?cgtcagcgcc???????????????????????????100

<210>57

<211>551

<212>DNA

＜213〉phage

<220>

<221>CDS

<222>(7)...(408)

＜221〉base of Xiu Shiing

<222>(1)...(1)

<223>n＝a，c，g，or?t

<400>57nagacc?atg?gct?tat?ggc?aga?aaa?aaa?aga?aga?cag?aga?aga?aga?atg????????48

Met?Ala?Tyr?Gly?Arg?Lys?Lys?Arg?Arg?Gln?Arg?Arg?Arg?Met

1???????????????5???????????????????10aac?gcg?ctg?cag?gaa?gat?acc?ccg?ccg?ggc?ccg?tcc?acc?gtg?ttt?cgc???????96Asn?Ala?Leu?Gln?Glu?Asp?Thr?Pro?Pro?Gly?Pro?Ser?Thr?Val?Phe?Arg?15??????????????????20??????????????????25??????????????????30ccg?ccg?acc?tcc?tcc?cgc?ccg?ctg?gaa?acc?ccg?cat?tgc?cgc?gaa?atc??????144Pro?Pro?Thr?Ser?Ser?Arg?Pro?Leu?Glu?Thr?Pro?His?Cys?Arg?Glu?Ile

35??????????????????40??????????????????45cgc?atc?ggc?atc?gcg?ggc?atc?acc?atc?acc?ctg?tcc?ctg?tgc?ggc?tgc??????192Arg?Ile?Gly?Ile?Ala?Gly?Ile?Thr?Ile?Thr?Leu?Ser?Leu?Cys?Gly?Cys

50??????????????????55??????????????????60gcg?aac?gcg?cgc?gcg?ccg?acc?ctg?cgc?tcc?gcg?acc?gcg?gat?aac?tcc??????240Ala?Asn?Ala?Arg?Ala?Pro?Thr?Leu?Arg?Ser?Ala?Thr?Ala?Asp?Asn?Ser

65??????????????????70??????????????????75gaa?aac?acc?ggc?ttt?aaa?aac?gtc?ccg?gat?ctg?cgc?acc?gat?cag?ccg??????288Glu?Asn?Thr?Gly?Phe?Lys?Asn?Val?Pro?Asp?Leu?Arg?Thr?Asp?Gln?Pro

80??????????????????85??????????????????90aaa?ccg?ccg?tcc?aaa?aaa?cgc?tcc?tgc?gat?ccg?tcc?gaa?tat?cgc?gtc??????336Lys?Pro?Pro?Ser?Lys?Lys?Arg?Ser?Cys?Asp?Pro?Ser?Glu?Tyr?Arg?Val?95?????????????????100?????????????????105?????????????????110tcc?gaa?ctg?aaa?gaa?tcc?ctg?atc?acc?acc?acc?ccg?tcc?cgc?ccg?cgc??????384Ser?Glu?Leu?Lys?Glu?Ser?Leu?Ile?Thr?Thr?Thr?Pro?Ser?Arg?Pro?Arg

115?????????????????120?????????????????125acc?gcc?cgc?cgc?tgc?atc?cgc?ctc?tgaaagcttg?gctgttttgg?cggatgagag?????438Thr?Ala?Arg?Arg?Cys?Ile?Arg?Leu

130aagattttca gcctgataca gattaaatca gaacgcagaa gcggtctgat aaaacagaat 498ttgcctggcg gcagtagcgc ggtggtccca cctgacccca tgccgaactc aga 551＜210〉58＜211〉134＜212〉PRT＜213〉bacteriophage＜400〉58Met Ala Tyr Gly Arg Lys Lys Arg Arg Gln Arg Arg Arg Met Asn Ala 15 10 15Leu Gln Glu Asp Thr Pro Pro Gly Pro Ser Thr Val Phe Arg Pro Pro

20??????????????????25??????????????????30Thr?Ser?Ser?Arg?Pro?Leu?Glu?Thr?Pro?His?Cys?Arg?Glu?Ile?Arg?Ile

35??????????????????40??????????????????45Gly?Ile?Ala?Gly?Ile?Thr?Ile?Thr?Leu?Ser?Leu?Cys?Gly?Cys?Ala?Asn

50??????????????????55??????????????????60Ala?Arg?Ala?Pro?Thr?Leu?Arg?Ser?Ala?Thr?Ala?Asp?Asn?Ser?Glu?Asn65??????????????????70??????????????????75??????????????????80Thr?Gly?Phe?Lys?Asn?Val?Pro?Asp?Leu?Arg?Thr?Asp?Gln?Pro?Lys?Pro

85??????????????????90??????????????????95Pro?Ser?Lys?Lys?Arg?Ser?Cys?Asp?Pro?Ser?Glu?Tyr?Arg?Val?Ser?Glu

100?????????????????105?????????????????110Leu?Lys?Glu?Ser?Leu?Ile?Thr?Thr?Thr?Pro?Ser?Arg?Pro?Arg?Thr?Ala

115?????????????????120?????????????????125Arg?Arg?Cys?Ile?Arg?Leu

130

<210>59

<211>444

<212>DNA

＜213〉phage

<220>

＜221〉base of Xiu Shiing

<222>(1)...(1)

<223>n＝a，c，g，or?t

<221>CDS

<222>(7)...(427)

<400>59nagacc?atg?gct?cat?cac?cat?cac?cac?cat?tat?ggc?cgc?aaa?aaa?cgc????????48

Met?Ala?His?His?His?His?His?His?Tyr?Gly?Arg?Lys?Lys?Arg

1???????????????5???????????????????10cgt?cag?cgc?cgt?cgc?atg?aac?gcg?ccg?cag?gaa?gat?acc?ccg?ccg?ggc???????96Arg?Gln?Arg?Arg?Arg?Met?Asn?Ala?Leu?Gln?Glu?Asp?Thr?Pro?Pro?Gly?15??????????????????20??????????????????25??????????????????30ccg?tcc?acc?gtg?ttt?cgc?ccg?ccg?acc?tcc?tcc?cgc?ccg?ctg?gaa?acc??????144Pro?Ser?Thr?Val?Phe?Arg?Pro?Pro?Thr?Ser?Ser?Arg?Pro?Leu?Glu?Thr

35??????????????????40??????????????????45ccg?cat?tgc?cgc?gaa?atc?cgc?atc?ggc?atc?gcg?ggc?atc?acc?atc?acc??????192Pro?His?Cys?Arg?Glu?Ile?Arg?Ile?Gly?Ile?Ala?Gly?Ile?Thr?Ile?Thr

50??????????????????55??????????????????60ctg?tcc?ctg?tgc?ggc?tgc?gcg?aac?gcg?cgc?gcg?ccg?acc?ctg?cgc?tcc??????240Leu?Ser?Leu?Cys?Gly?Cys?Ala?Asn?Ala?Arg?Ala?Pro?Thr?Leu?Arg?Ser

65??????????????????70??????????????????75gcg?acc?gcg?gat?aac?tcc?gaa?aac?acc?ggc?ttt?aaa?aac?gtc?ccg?gat??????288Ala?Thr?Ala?Asp?Asn?Ser?Glu?Asn?Thr?Gly?Phe?Lys?Asn?Val?Pro?Asp

80??????????????????85??????????????????90ctg?cgc?acc?gat?cag?ccg?aaa?ccg?ccg?tcc?aaa?aaa?cgc?tcc?tgc?gat??????336Leu?Arg?Thr?Asp?Gln?Pro?Lys?Pro?Pro?Ser?Lys?Lys?Arg?Ser?Cys?Asp?95?????????????????100?????????????????105?????????????????110ccg?tcc?gaa?tat?cgc?gtc?tcc?gaa?ctg?aaa?gaa?tcc?ctg?atc?acc?acc??????384Pro?Ser?Glu?Tyr?Arg?Val?Ser?Glu?Leu?Lys?Glu?Ser?Leu?Ile?Thr?Thr

115?????????????????120?????????????????125acc?ccg?tcc?cgc?ccg?cgc?acc?gcc?cgc?cgc?tgc?atc?cgc?ctc?t????????????427Thr?Pro?Ser?Arg?Pro?Arg?Thr?Ala?Arg?Arg?Cys?Ile?Arg?Leu

130 135 140gaaagcttgg ctgtttt 444＜210〉60＜211〉140＜212〉PRT＜213〉bacteriophage＜400〉60Met Ala His His His His His His Tyr Gly Arg Lys Lys Arg Arg Gln, 15 10 15Arg Arg Arg Met Asn Ala Leu Gln Glu Asp Thr Pro Pro Gly Pro Ser

20??????????????????25??????????????????30Thr?Val?Phe?Arg?Pro?Pro?Thr?Ser?Ser?Arg?Pro?Leu?Glu?Thr?Pro?His

35??????????????????40??????????????????45Cys?Arg?Glu?Ile?Arg?Ile?Gly?Ile?Ala?Gly?Ile?Thr?Ile?Thr?Leu?Ser

50??????????????????55??????????????????60Leu?Cys?Gly?Cys?Ala?Asn?Ala?Arg?Ala?Pro?Thr?Leu?Arg?Ser?Ala?Thr65??????????????????70??????????????????75??????????????????80Ala?Asp?Asn?Ser?Glu?Asn?Thr?Gly?Phe?Lys?Asn?Val?Pro?Asp?Leu?Arg

85??????????????????90?????????????????95Thr?Asp?Gln?Pro?Lys?Pro?Pro?Ser?Lys?Lys?Arg?Ser?Cys?Asp?Pro?Ser

100?????????????????105?????????????????110Glu?Tyr?Arg?Val?Ser?Glu?Leu?Lys?Glu?Ser?Leu?Ile?Thr?Thr?Thr?Pro

115?????????????????120?????????????????125Ser?Arg?Pro?Arg?Thr?Ala?Arg?Arg?Cys?Ile?Arg?Leu

130 135 140＜210〉61＜211〉1565＜212〉DNA＜213〉 ( salmonella )＜400〉61gatatcattc tggcctctga cgttgtgatg gtcgcacgtg gcgatctggg cgttgaaatc 60ggcgatccgg agctggttgg tatccagaaa gcgctgattc gccgtgcgcg tcagctaaac 120cgcgcagtca tcaccgcaac gcaaatgatg gagtcgatga tcaccaaccc gatgccgacc 180cgtgcggaag tgatggacgt ggcgaacgcc gtcctggatg gcacggatgc ggttatgctg 240tctgccgaaa ccgcagccgg tcagtatcct tctgaaaccg ttgccgcaat ggcgcgcgtc 300tgcctgggcg cagaaaaaat ccccagcatc aatgtgtcta aacaccgtct cgacgtgcag 360ttcgacaacg ttgaagaagc cattgccatg tctgcgatgt atgcggcaaa ccatctgaaa 420ggcgttaccg cgatcatcac catgacggaa tccggtcgta ccgcgctaat gacttcccgt 480atcagctccg gcctgccgat tttcgccatg tcgcgccatg aacgcacgct gaacctgacc 540gcgctctatc gcggagtaac gccggtgcat tttgatagcg cggctgatgg cgttgtcgcg 600gcacatgaag ctgttaatct gctgcgcgat aaagggtatc tggtttccgg cgacctggtt 660atcgtgaccc agggcgatgt catgagcacc gtcggttcaa ccaataccac gcggccgccc 720ccttaattaa ccccgcatgc ggggggccat ataggccggg gatttaaatg caaacgtccg 780ccgaaacgcc gacgcactgt gttccagata tagtcaaaaa ccggattacc ctgattatga 840aacatcgccg ccattttttg cccctgagag gccatcagca tggctggaat gtcgacgccc 900cagccatgcg gtacgagaaa aatgactttt tcgtcgttac gacgcatctc ctcgataatc 960tccagacctt cccagtcaac acgctgttga atttttttcg gaccgcgcat cgccaactca 1020gccatcatcg ccattgcctg tggcgcggtg gcgaacatct catcgacaat cgcttcgcgc 1080tcagcttcgc tacgctgcgg aaagcacaac gacagattaa ttagcgcccg gcgacgagaa 1140ctcttcccca gccgtccggc aaaacgcccc agcgtcgcca gcaaagggtc gcggaatgat 1200gccggtgtta atgcgatccc cgccattgcc gccgcgccca accaggcgcc ccaatactgt 1260ggatagcgaa aggatttttc gaattcaggg atatactcac tattattttt tttggtttcc 1320atgcttttcc agggtctgct gacgcgaaaa ggaattgtga atagtgtagc gacgtctgcg 1380tctcacacaa aacaaaaaag ccggcacaca tcgcgtaccg gctctgtcag cgcatttgtt 1440aatcgaagcg cagttgcggc agaacctctt tcacctgtgc caggtattca cgacgatctg 1500accccgtcag accttccgtg cgcggcaatt ttgctgtcag agggttaacg gcttgctggt 1560tgatc 1565

Claims

1. attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

2. attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding and one or more second order effect molecules, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

3. claim 1 or 2 the attenuated bacteria that is oriented to tumor, wherein at least a primary effector molecule is the TNF family member.

4. the attenuated bacteria that is oriented to tumor of claim 3, wherein the TNF family member is tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis, CD40 part (CD40L), LT-α, LT-β, OX40L, CD40L, FasL, CD27L, CD30L, 4-1BBL, APRIL, LIGHT, TL1, TNFSF16, TNFSF17 or AITR-L.

5. claim 1 or 2 the attenuated bacteria that is oriented to tumor, wherein at least a primary effector molecule is an anti-angiogenesis.

6. the attenuated bacteria that is oriented to tumor of claim 5, wherein anti-angiogenesis is interior chalone, angiostatin, the angiogenesis inhibitor Antithrombin III, the 29kDa N-end protein hydrolysis fragment of fibronectin and 40kDa C-end protein hydrolysis fragment, the uPA receptor antagonist, the 16kDa proteolytic fragments of prolactin antagonist, the 7.8kDa proteolytic fragments of PF4, PF4 contain 24 amino acid whose angiogenesis inhibitor fragments, be called as 13.40 anti-angiogenesis, thrombospondin I's contains 22 amino acid whose angiogenesis inhibitor fragments of peptides, SPARC's contains 20 amino acid whose angiogenesis inhibitor fragments of peptides, the peptide that contains RGD and NGR, the angiogenesis inhibitor small-molecular peptides of laminin, the angiogenesis inhibitor small-molecular peptides of fibronectin, precollagenous angiogenesis inhibitor small-molecular peptides, the angiogenesis inhibitor small-molecular peptides of EGF, and beta 2 integrin alpha _vβ ₃Peptide antagonists or the peptide antagonists of vegf receptor.

7. claim 1 or 2 the attenuated bacteria that is oriented to tumor, wherein at least a primary effector molecule is the bacteriocin family member, condition is that this bacteriocin is not BRP.

8. the attenuated bacteria that is oriented to tumor of claim 7, wherein the bacteriocin family member is the plain M15 of ColE1, ColE1a, ColE1b, ColE2, ColE3, ColE4, ColE5, ColE6, ColE7, ColE8, ColE9, colicine A, colicine K, colicine L, colicine M, cloacin DF13, pesticin A1122, staphylococcin 1580, butyricin 7423, pyocin R1 or AP41, megacin A-216, vibriobactins Vibriobactin. or microorganism.

9. claim 1 or 2 the attenuated bacteria that is oriented to tumor, wherein primary effector molecule is the tumor suppression enzyme.

10. the attenuated bacteria that is oriented to tumor of claim 9, wherein the tumor suppression enzyme is methioninase, asparaginase, lipase, phospholipase, protease, DNA enzyme or glycosidase.

11. the attenuated bacteria that is oriented to tumor of claim 1 or 2, wherein primary effector molecule is hemolysin, Vero cytotoxin, CNF1, CNF2 or PMT.

12. the attenuated bacteria that is oriented to tumor of claim 1 or 2, wherein primary effector molecule derives from animal, plant, antibacterial or virus.

13. the attenuated bacteria that is oriented to tumor of claim 2, wherein the second order effect molecule is immunomodulator, anti-tumor protein, prodrug invertase, antisense molecule, ribozyme or antigen.

14. the attenuated bacteria that is oriented to tumor of claim 1 or 2, the attenuated bacteria that wherein is oriented to tumor is a Salmonella.

15. the attenuated bacteria that is oriented to tumor of claim 1, the attenuated bacteria that wherein is oriented to tumor contains a kind of enhancing delivery system in addition.

16. the attenuated bacteria that is oriented to tumor of claim 2, wherein the second order effect molecule is bacteriocin releasing factor (BRP).

17. attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more fusion rotein of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains a kind of signal sequence and a kind of effector molecule.

18. attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more fusion rotein of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains a kind of peptide and a kind of effector molecule of transporting.

19. the attenuated bacteria that is oriented to tumor of claim 18, wherein fusion rotein contains a kind of signal sequence in addition.

20. the attenuated bacteria that is oriented to tumor of claim 17 or 19, wherein signal sequence is a kind of OmpA sample albumen.

21. the attenuated bacteria that is oriented to tumor of claim 18 or 19 wherein transports peptide and derives from HIV TAT albumen, feeler foot homeodomain (penetrating albumen), Ka Boxi fibroblast growth factor (FGF) membrane translocation sequence (MTS), herpes simplex virus VP22, six polyhistidyls, six polylysines or six poly arginines.

22. claim 17,18 or 19 the attenuated bacteria that is oriented to tumor, wherein effector molecule is primary effector molecule or second order effect molecule.

23. claim 17,18 or 19 the attenuated bacteria that is oriented to tumor, the attenuated bacteria that wherein is oriented to tumor contains one or more nucleic acid molecules that are connected with one or more promoter operability in addition, described one or more effector molecules of nucleic acid molecules codified.

24. the attenuated bacteria that is oriented to tumor of claim 23, wherein effector molecule is primary effector molecule or second order effect molecule.

25. Pharmaceutical composition, said composition contains pharmaceutically suitable carrier and is oriented to the attenuated bacteria of tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

26. Pharmaceutical composition, said composition contains pharmaceutically suitable carrier and is oriented to the attenuated bacteria of tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding and one or more second order effect molecules, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

27. the Pharmaceutical composition of claim 25 or 26, wherein at least a primary effector molecule is the TNF family member.

28. the Pharmaceutical composition of claim 27, wherein the TNF family member is tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis, CD40 part (CD40L), LT-α, LT-β, OX40L, CD40L, FasL, CD27L, CD30L, 4-1BBL, APRIL, LIGHT, TL1, TNFSF16, TNFSF17 or AITR-L.

29. the Pharmaceutical composition of claim 25 or 26, wherein at least a primary effector molecule is an anti-angiogenesis.

30. the Pharmaceutical composition of claim 29, wherein anti-angiogenesis is interior chalone, angiostatin, the angiogenesis inhibitor Antithrombin III, the 29kDa N-end protein hydrolysis fragment of fibronectin and 40kDa C-end protein hydrolysis fragment, the uPA receptor antagonist, the 16kDa proteolytic fragments of prolactin antagonist, the 7.8kDa proteolytic fragments of PF4, PF4 contain 24 amino acid whose angiogenesis inhibitor fragments, be called as 13.40 anti-angiogenesis, thrombospondin I's contains 22 amino acid whose angiogenesis inhibitor fragments of peptides, SPARC's contains 20 amino acid whose angiogenesis inhibitor fragments of peptides, the peptide that contains RGD and NGR, the angiogenesis inhibitor small-molecular peptides of laminin, the angiogenesis inhibitor small-molecular peptides of fibronectin, precollagenous angiogenesis inhibitor small-molecular peptides, the angiogenesis inhibitor small-molecular peptides of EGF, and beta 2 integrin alpha _vβ ₃Peptide antagonists or the peptide antagonists of vegf receptor.

31. the Pharmaceutical composition of claim 25 or 26, wherein at least a primary effector molecule is the bacteriocin family member, and condition is that this bacteriocin is not BRP.

32. the Pharmaceutical composition of claim 31, wherein the bacteriocin family member is the plain M15 of ColE1, ColE1a, ColE1b, ColE2, ColE3, ColE4, ColE5, ColE6, ColE7, ColE8, ColE9, colicine A, colicine K, colicine L, colicine M, cloacin DF13, pesticin A1122, staphylococcin 1580, butyricin 7423, pyocin R1 or AP41, megacin A-216, vibriobactins Vibriobactin. or microorganism.

33. the Pharmaceutical composition of claim 25 or 26, wherein at least a primary effector molecule is the tumor suppression enzyme.

34. the Pharmaceutical composition of claim 33, wherein the tumor suppression enzyme is methioninase, asparaginase, lipase, phospholipase, protease, DNA enzyme or glycosidase.

35. the Pharmaceutical composition of claim 25 or 26, wherein at least a primary effector molecule are hemolysin, Vero cytotoxin, CNF1, CNF2 or PMT.

36. the Pharmaceutical composition of claim 25 or 26, wherein primary effector molecule derives from animal, plant, antibacterial or virus.

37. the Pharmaceutical composition of claim 26, wherein the second order effect molecule is immunomodulator, anti-tumor protein, prodrug invertase, antisense molecule, ribozyme or antigen.

38. the Pharmaceutical composition of claim 25 or 26, the attenuated bacteria that wherein is oriented to tumor is a Salmonella.

39. the Pharmaceutical composition of claim 25, the attenuated bacteria that wherein is oriented to tumor contains a kind of enhancing delivery system in addition.

40. the Pharmaceutical composition of claim 26, wherein the second order effect molecule is the bacteriocin releasing factor.

41. Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more fusion rotein of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains signal sequence and effector molecule.

42. Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more fusion rotein of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains and transports peptide and effector molecule.

43. the Pharmaceutical composition of claim 42, wherein fusion rotein contains a kind of signal sequence in addition.

44. the Pharmaceutical composition of claim 41 or 43, wherein signal sequence is a kind of OmpA sample albumen.

45. the Pharmaceutical composition of claim 42 or 43 wherein transports peptide and derives from HIV TAT albumen, feeler foot homeodomain (penetrating albumen), Ka Boxi fibroblast growth factor (FGF) membrane translocation sequence (MTS), herpes simplex virus VP22, six polyhistidyls, six polylysines or six poly arginines.

46. claim 41,42 or 43 Pharmaceutical composition, wherein effector molecule is primary effector molecule or second order effect molecule.

47. claim 41,42 or 43 Pharmaceutical composition, the attenuated bacteria that wherein is oriented to tumor contains one or more nucleic acid molecules that are connected with one or more promoter operability in addition, described one or more effector molecules of nucleic acid molecules codified.

48. be used for one or more primary effector molecules of treatment solid tumor cancer are delivered to the experimenter's of this treatment of needs method, this method comprises and gives a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

49. be used for one or more primary effector molecules of treatment solid tumor cancer and the method that one or more second order effect molecules are delivered to the experimenter of this treatment of needs, this method comprises and gives a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding and one or more second order effect molecules, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

50. the method for claim 48 or 49, wherein at least a primary effector molecule is the TNF family member.

51. the method for claim 50, wherein the TNF family member is tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis, CD40 part (CD40L), LT-α, LT-β, OX40L, CD40L, FasL, CD27L, CD30L, 4-1BBL, APRIL, LIGHT, TL1, TNFSF16, TNFSF17 or AITR-L.

52. the method for claim 48 or 49, wherein at least a primary effector molecule is an anti-angiogenesis.

53. the method for claim 52, wherein anti-angiogenesis is interior chalone, angiostatin, the angiogenesis inhibitor Antithrombin III, the 29kDa N-end protein hydrolysis fragment of fibronectin and 40kDa C-end protein hydrolysis fragment, the uPA receptor antagonist, the 16kDa proteolytic fragments of prolactin antagonist, the 7.8kDa proteolytic fragments of PF4, PF4 contain 24 amino acid whose angiogenesis inhibitor fragments, be called as 13.40 anti-angiogenesis, thrombospondin I's contains 22 amino acid whose angiogenesis inhibitor fragments of peptides, SPARC's contains 20 amino acid whose angiogenesis inhibitor fragments of peptides, the peptide that contains RGD and NGR, the angiogenesis inhibitor small-molecular peptides of laminin, the angiogenesis inhibitor small-molecular peptides of fibronectin, precollagenous angiogenesis inhibitor small-molecular peptides, the angiogenesis inhibitor small-molecular peptides of EGF, and beta 2 integrin alpha _vβ ₃Peptide antagonists or the peptide antagonists of vegf receptor.

54. the method for claim 48 or 49, wherein at least a primary effector molecule is the bacteriocin family member, and condition is that this bacteriocin is not BRP.

55. the method for claim 54, wherein the bacteriocin family member is the plain M15 of ColE1, ColE1a, ColE1b, ColE2, ColE3, ColE4, ColE5, ColE6, ColE7, ColE8, ColE9, colicine A, colicine K, colicine L, colicine M, cloacin DF13, pesticin A1122, staphylococcin 1580, butyricin 7423, pyocin R1 or AP41, megacin A-216, vibriobactins Vibriobactin. or microorganism.

56. the method for claim 48 or 49, wherein at least a primary effector molecule is the tumor suppression enzyme.

57. the method for claim 56, wherein the tumor suppression enzyme is methioninase, asparaginase, lipase, phospholipase, protease, DNA enzyme or glycosidase.

58. the method for claim 48 or 49, wherein at least a primary effector molecule are hemolysin, Vero cytotoxin, CNF1, CNF2 or PMT.

59. the method for claim 48 or 49, wherein primary effector molecule derives from animal, plant, antibacterial or virus.

60. the method for claim 49, wherein at least a second order effect molecule are anti-tumor protein, prodrug invertase, antisense molecule, ribozyme or antigen.

61. the method for claim 48 or 49, the attenuated bacteria that wherein is oriented to tumor is a Salmonella.

62. the method for claim 48, the attenuated bacteria that wherein is oriented to tumor contains a kind of enhancing delivery system in addition.

63. the method for claim 49, wherein the second order effect molecule is the bacteriocin releasing factor.

64. be used for one or more fusion rotein of treatment solid tumor cancer are delivered to the experimenter's of this treatment of needs method, this method comprises and gives a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, described one or more fusion rotein of nucleic acid molecules codified, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains a kind of signal sequence and a kind of effector molecule.

65. be used for one or more fusion rotein of treatment solid tumor cancer are delivered to the experimenter's of this treatment of needs method, this method comprises and gives a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, described one or more fusion rotein of nucleic acid molecules codified, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains a kind of peptide and a kind of effector molecule of transporting.

66. the method for claim 65, wherein fusion rotein contains a kind of signal sequence in addition.

67. the method for claim 64 or 66, wherein signal sequence is a kind of OmpA sample albumen.

68. the method for claim 65 or 66 is wherein transported peptide and is derived from HIV TAT albumen, feeler foot homeodomain (penetrating albumen), Ka Boxi fibroblast growth factor (FGF) membrane translocation sequence (MTS), herpes simplex virus VP22, six polyhistidyls, six polylysines or six poly arginines.

69. claim 64,65 or 66 method, wherein effector molecule is primary effector molecule or second order effect molecule.

70. claim 64,65 or 66 method, the attenuated bacteria that wherein is oriented to tumor contains one or more nucleic acid molecules that are connected with one or more promoter operability in addition, one or more effector molecules of described nucleic acid molecule encoding.

71. be used for the treatment of the method for the intravital solid tumor cancer of animal, this method comprises and gives one or more chemotherapeutics and a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

72. be used for the treatment of the method for the intravital solid tumor cancer of animal, this method comprises and gives one or more chemotherapeutics and a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more primary effector molecules of described nucleic acid molecule encoding and one or more second order effect molecules, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe.

73. the method for claim 71 or 72, wherein at least a primary effector molecule is the TNF family member.

74. the method for claim 73, wherein the TNF family member is tumor necrosis factor-alpha (TNF-α), tumor necrosis factor-β (TNF-β), the cytokine (TRANCE) of the relevant activation-inducing of TNF-α apoptosis induction ligand related (TRAIL), TNF-α, the weak inducer (TWEAK) of TNF-α related apoptosis, CD40 part (CD40L), LT-α, LT-β, OX40L, CD40L, FasL, CD27L, CD30L, 4-1BBL, APRIL, LIGHT, TL1, TNFSF16, TNFSF17 or AITR-L.

75. the method for claim 71 or 72, wherein at least a primary effector molecule is a kind of anti-angiogenesis.

76. the method for claim 75, wherein anti-angiogenesis is interior chalone, angiostatin, the angiogenesis inhibitor Antithrombin III, the 29kDa N-end protein hydrolysis fragment of fibronectin and 40kDa C-end protein hydrolysis fragment, the uPA receptor antagonist, the 16kDa proteolytic fragments of prolactin antagonist, the 7.8kDa proteolytic fragments of PF4, PF4 contain 24 amino acid whose angiogenesis inhibitor fragments, be called as 13.40 anti-angiogenesis, thrombospondin I's contains 22 amino acid whose angiogenesis inhibitor fragments of peptides, SPARC's contains 20 amino acid whose angiogenesis inhibitor fragments of peptides, the peptide that contains RGD and NGR, the angiogenesis inhibitor small-molecular peptides of laminin, the angiogenesis inhibitor small-molecular peptides of fibronectin, precollagenous angiogenesis inhibitor small-molecular peptides, the angiogenesis inhibitor small-molecular peptides of EGF, and beta 2 integrin alpha _vβ ₃Peptide antagonists or the peptide antagonists of vegf receptor.

77. the method for claim 71 or 72, wherein at least a primary effector molecule is the bacteriocin family member, and condition is that this bacteriocin is not BRP.

78. the method for claim 77, wherein the bacteriocin family member is the plain M15 of ColE1, ColE1a, ColE1b, ColE2, ColE3, ColE4, ColE5, ColE6, ColE7, ColE8, ColE9, colicine A, colicine K, colicine L, colicine M, cloacin DF13, pesticin A1122, staphylococcin 1580, butyricin 7423, pyocin R1 or AP41, megacin A-216, vibriobactins Vibriobactin. or microorganism.

79. the method for claim 71 or 72, wherein at least a primary effector molecule is the tumor suppression enzyme.

80. the method for claim 79, wherein the tumor suppression enzyme is methioninase, asparaginase, lipase, phospholipase, protease, DNA enzyme or glycosidase.

81. the method for claim 71 or 72, wherein at least a primary effector molecule are hemolysin, Vero cytotoxin, CNF1, CNF2 or PMT.

82. the method for claim 71 or 72, wherein primary effector molecule derives from animal, plant, antibacterial or virus.

83. the method for claim 82, wherein the second order effect molecule is immunomodulator, anti-tumor protein, prodrug invertase, antisense molecule, ribozyme, or antigen.

84. the method for claim 71 or 72, the attenuated bacteria that wherein is oriented to tumor is a Salmonella.

85. the method for claim 71, the attenuated bacteria that wherein is oriented to tumor contains a kind of enhancing delivery system in addition.

86. the method for claim 72, wherein the second order effect molecule is the bacteriocin releasing factor.

87. be used for the treatment of the method for the intravital solid tumor cancer of animal, this method comprises and gives one or more chemotherapeutics and a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more fusion rotein of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains a kind of signal sequence and a kind of effector molecule.

88. be used for the treatment of the method for the intravital solid tumor cancer of animal, this method comprises and gives one or more chemotherapeutics and a kind of Pharmaceutical composition, said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor, this antibacterial contains one or more nucleic acid molecules that are connected with one or more promoter operability, one or more fusion rotein of described nucleic acid molecule encoding, wherein, the described attenuated bacteria that is oriented to tumor is a kind of facultative aerobe or facultative anaerobe, and described fusion rotein contains a kind of peptide and a kind of effector molecule of transporting.

89. the method for claim 88, wherein fusion rotein contains a kind of signal sequence in addition.

90. the method for claim 87 or 89, wherein signal sequence is a kind of OmpA sample albumen.

91. the method for claim 88 or 89 is wherein transported peptide and is derived from HIV TAT albumen, feeler foot homeodomain (penetrating albumen), Ka Boxi fibroblast growth factor (FGF) film transfer bit sequence (MTS), herpes simplex virus VP22, six polyhistidyls, six polylysines or six poly arginines.

92. claim 87,88 or 89 method, effector molecule wherein is a kind of primary effector molecule or second order effect molecule.

93. claim 87,88 or 89 method, the attenuated bacteria that wherein is oriented to tumor contains one or more nucleic acid molecules that are connected with one or more promoter operability in addition, described one or more effector molecules of nucleic acid molecules codified.

94. be used for the treatment of the method for the intravital solid tumor cancer of animal, this method comprises and gives one or more chemotherapeutics and a kind of Pharmaceutical composition that said composition contains a kind of pharmaceutically suitable carrier and a kind of attenuated bacteria that is oriented to tumor.

95. a fusion rotein, this fusion rotein contain a kind of OmpA sample albumen and a kind of effector molecule.

96. a fusion rotein, this fusion rotein contain a kind of signal sequence, a kind of peptide and a kind of effector molecule of transporting.

97. the fusion rotein of claim 96, wherein signal sequence is a kind of OmpA sample albumen.

98. the fusion rotein of claim 96 wherein transports peptide and derives from HIV TAT albumen, feeler foot homeodomain (penetrating albumen), Ka Boxi fibroblast growth factor (FGF) film metastasis sequence (MTS), herpes simplex virus VP22, six polyhistidyls, six polylysines or six poly arginines.

99. the fusion rotein of claim 95 or 96, wherein effector molecule is primary effector molecule or second order effect molecule.