NZ515493A - Conformationally constrained backbone cyclized interleukin-6 antagonists - Google Patents
Conformationally constrained backbone cyclized interleukin-6 antagonistsInfo
- Publication number
- NZ515493A NZ515493A NZ515493A NZ51549300A NZ515493A NZ 515493 A NZ515493 A NZ 515493A NZ 515493 A NZ515493 A NZ 515493A NZ 51549300 A NZ51549300 A NZ 51549300A NZ 515493 A NZ515493 A NZ 515493A
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- NZ
- New Zealand
- Prior art keywords
- arg
- lys
- phe
- leu
- antagonist
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
- C07K14/54—Interleukins [IL]
- C07K14/5412—IL-6
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/715—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons
- C07K14/7155—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons for interleukins [IL]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Abstract
A pharmaceutical composition containing a backbone cyclised peptide analog having IL-6 antagonist activity, having a peptide sequence of five to twenty amino acids that incorporates at least one building unit; said unit containing one nitrogen atom of the peptide backbone connected to a bridging group comprising an amide, thioether, thioester or disulphide; the building unit is connected via the bridging group to form a cyclic structure with a moiety selected from: a second building unit, the side chain of an amino acid residue of the sequence or the N-terminal amino acid residue; for use against neoplasms, bacterial, parasitic and viral infection, chronic autoimmune disorders and osteoporosis.
Description
WO 00/72864 PCT/ILOO/00305
CONFORMATIONAL]!Y CONSTRAINED BACKBONE CYCLIZED INTERLEUKIN-6 ANTAGONISTS
FIELD OF THE INVENTION
The present invention relates to conformationally constrained backbone-cyclized IL-6 antagonists, and to pharmaceutical compositions containing same.
BACKGROUND OF THE INVENTION
Interleukin-6 (IL-6) is a member of the helical cytokine family. IL-6 is produced by almost all cell types in response to a variety of different stimuli including bacterial (LPS) and viral infections, cancer, and other cytokines (e.g. IL-1). IL-6 is a pleiotropic factor, it participates in numerous processes and is thus associated with numerous disorders (for a review see Hirano T., Intern. Rev. Immunol. 16:249, 1998).
Bioactivity of IL-6 requires interaction of the cytokine, IL-6, its receptor (IL-6R) and a transmembrane signal transducer known as glycoprotein 130 (gpl30), and formation of a hexameric complex containing two units of each protein. The outcome of the complex formation is dimerization of gp!30, which by itself is sufficient for obtaining IL-6 like bioactivity (Fourcin, et al., J. Biol. Chem. 271: 11756, 1996.). Several other cytokines also use gpl30 for signal transduction. These include: interleukin-11 (IL-11), ciliary neurotrophic factor . (CNTF), leukocyte inhibitory factor (LIF), oncostatin M (OSM).
IL-6 and host defense
IL-6 levels increases early during bacterial and viral infections. IL-6 induces production of acute phase proteins which are thought to participate in the defense of the host organism against tissue damage and infection. The acute phase response is considered to be the systemic inflammatory reaction to infection and injury.
IL-6 also amplifies the immune system through its multiple growth and differentiation activities such as induction of B
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cell differentiation, replication of bone marrow progenitor cells, and augmentation of T lymphocytes, including enhancement of cytotoxic T lymphocytes.
IL-6 in homeostasis, injury and transplantation:
IL-6 levels are increased during stress. IL-6 in rabbits is directly responsible for elevation of body temperature. High IL-6 levels in burn patients correlates with mortality.
Elevated IL-6 levels are associated with traumatic events and 10 allograft rejection.
IL-6 in Osteoporosis:
Estrogen plays an important role in maintaining bone mass. A massive loss of bone mass is reported in women at there 15 postmenopausal stage. Increased bone resorption and increased osteoclast activity in postmenopausal osteoporosis have been-linked with IL-6. The production of IL-6 is elevated in bone marrow cells at this stage correlating the fact that estrogen down regulates IL-6 gene expression. Estrogen loss induced by 20 ovariectomy in mice enhances osteoclast development and this change can be prevented by antibodies to IL-6. Several experiments including an IL-6 knockout mice model, treatment with anti IL-6 antibodies or with IL-6 antisense demonstrate that elevated levels of IL-6 plays a critical role in the 25 formation of osteoclastic cells. As such, dysregulation of IL-6 activity in bone cells leads to the development of pathological disease.
IL-6 in immune disorders 30 Elevated levels of IL-6 in cardiac myxoma and cervical carcinoma are associated with autoimmunity indications such as: production of anti-nuclear factor, rheumatoid factors, elevated immune complexes, arthritis and nephritis.
Castelman's disease patients suffer form fever, anemia,
hyper-y-globulinemia, and an increase in acute phase proteins.
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The lymph nodes constitutively produce large amounts of IL-6, and surgical removal of the involved lymph nodes is followed by decrease in serum IL-6 levels and a dramatic clinical improvement. It has been demonstrated that systemic 5 manifestation of Castelman's disease could'be alleviated by treatment with anti-IL-6 antibody.
Local and general symptoms of rheumatoid arthritis, such as plasma cell infiltration into synovial tissues, autoantibody 10 production, and polyclonal hyper-y-globulinemia can be explained by increased IL-6 production observed in synovial tissue. At least two mediators which are elevated in RA patients, PGE2 and IL-1, are known to induce synthesis of IL-6. Higher than normal levels of IL-6 have been detected in sera of 15 patients with active SLE. Increased plasma levels of IL-6 were observed in psoriasis patients.
AIDS:
High levels of IL-6 are associated with HIV infection. The HIV 20 envelope glycoproteins gpl20 and gpl60 induce IL-6 production from CD4+ T cells. Is has been demonstrated that IL-6 is a growth factor of the AIDS associated Kaposi's sarcoma (Murakamin-Mori, et al. Int. Immunol. 8: 595, 1996). The soluble form of the IL-6 receptor (sIL-6Ra) is a potent growth 25 factor for AIDS-associated Kaposi's sarcoma (KS) cells. The soluble form of gpl30 is antagonistic for sIL-6Ra-induced AIDS-KS cell growth. Furthermore, high IL-6 levels are associated with weight loss in AIDS.
Proliferative diseases and malignancies
An autocrine role for IL-6 has been reported in several types of cancer, among which are renal cell carcinoma, Hodgkin and non-Hodgkin's lymphoma, chronic lymphocytic leukemia, and acute myeloid leukemias. Plasmacytoma and myeloma cells require IL-6 35 for growth. Treatment of primary plasma cell leukemia with anti-IL-6 antibodies improves the patient's clinical status
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throughout the treatment. Also, IL-6 deficient mice are completely resistant to plasmacytoma induction.
Multiple myeloma is a malignant proliferation of plasma cells derived from a single clone. It is manifested in a number of organ dysfunctions and symptoms of bone pain or fractures, hypercalcemia, renal failure, susceptibility to infection, anemia and bleeding. The disease typically follows a chronic course for 2 to 5 years before progressing into an acute terminal phase.
The different therapeutic strategies for inhibition of multiple myeloma have been recently reviewed (Ogata A., Leuk. Res. 20 : 303, 1996). The vast majority of multiple myeloma patients require systemic chemotherapy to control the malignancy, and symptomatic supportive care to minimize the morbidity. The outcome of patients with multiple myeloma is still unsatisfactory, with median survival times of 2 to 3 years. Clearly, there is a need for an agent that cannot only improve the chances of remission, but also increase the duration of response and enhance survival.
Recently, injection of an anti-IL-6 antibody was tested in young population and resulted in a complete blocking of myeloma cell proliferation and inhibition of the serum IL-6 bioactivity. However, the administration of a single anti-IL-6 mAb appeared to be insufficient (Klein, et al., Blood 85: 863, 1995).
IL-6 has also a regulatory role in activation of Matrix Metalloproteinases (MMPs). MMPs are enzymes that are capable degrading the basement membrane components. As such MMPs are refereed as key enzymes in Extra Cellular Matrix remodeling, tumor invasion and metastasis.
Inhibitors of IL-6 activity
It is generally accepted that IL-6 inhibitors have clinical value. As indicated above there are a number of clinical situations where IL-6 inhibitors could be of therapeutic use. Most of the attempts to produced inhibitors to IL-6 reported in
WO 00/72864 PCT/IL00/00305
the literature in the past, used proteins. In general, proteins are not very suitable as drugs, due to their immunogenic potential, high cost, and the necessity for parenteral administration. The various attempts to use proteins to inhibit IL-6 are described below.
Monoclonal antibodies and antibody fragments:
The most common approach is to use monoclonal antibodies (mAbs). Several murine mAbs capable of inhibiting the bioactivity of IL-6 have been described.
The drawbacks in the use of antibodies against IL-6 are that the mAb traps the IL-6 in an immune complex in the circulation (May et al., J. Immunol. 151, 3225, 1993), thereby increasing its half-life 200-fold (Lu et al., Blood 86, 3123,1995). The immune complexes are thus serve as long term, slow release deposits of IL-6. The presence of high levels of circulating immune complexes could result in their precipitation in the basal lamina in the kidneys or in the joints, which could lead to kidney failure or arthritis.
Attempts to block IL-6 with monoclonal antibodies have been reported for the following diseases: AIDS associated syndromes and lymphoma (Emilie, et al., Blood 84: 2472, 1994),
Castelman's disease, rheumatoid arthritis (Wijdenes et al., J. Interferon Res. 14: 297, 1994, Yoshizaki et al. Springer Semin. Tmmunopatho.1., 2-0:247, 1998), multiple myeloma, plasma cell leukemia (Klein et al., Blood 78 : 1198, 1991), and endotoxin toxicity. Partial response were observe in most instances, but the problems associated with the use of monoclonal antibodies for inhibition of IL-6 have so far prevented their routine clinical application.
Some of problems associated with the clinical use of monoclonal antibodies are a result of the large size of the antibody molecule. Minibodies which utilize the hypervariable loop structure of antibodies, capable of inhibiting IL-6 bioactivity were recently reported (Martin et al., The EMBO J. 13, 5303, 1994). Binding of IL-6 to a minibody molecule should create a
WO 00/72864 PCT/IL00/00305
complex that is small enough to be secreted from the kidney, thereby decreasing the risk of creating slow release IL-6 deposits. Minibody-IL-6 complexes may not be recognized as immune complexes, thereby decreasing the chances for kidneys 5 and arthritic problems. The minibodies could still be immunogenic and it is unlikely that they will be orally available. So far, minibodies with sufficiently high affinity for IL-6 have not been obtained.
Mutated proteins:
Several IL-6 mutants were selected for desired activity using phage display systems. Super active mutants were reported (Toniatti, et al., The EMBO J. 15: 2726, 1996) as well as mutants which retain the capacity for binding of the IL-6R but lose the ability for interaction with the gpl30 and thus could serve as functional antagonists of IL-6 bioactivity (Savino et al., The EMBO J. 13,5863, 1994; Sporeno, et al., Blood 87: 4 510, 1996). The danger in clinical use of such mutants is the formation of antibodies that would recognize both the mutated and the native molecules. Such antibodies could block the bioactivity of IL-6 long after the treatment is terminated thereby exposing the patients to danger associated with lack of IL-6.
US Patent No. 5,470,952 disclose CTNF and IL-6 antagonists which are heterodimer proteins comprising a soluble a specificity determining cytokine receptor component and the extracellular domain of a p receptor component. Specifically, the inventors claim an IL-6 antagonist, capable of binding IL-6 to form a nonfunctional complex, comprising: soluble IL-6Ra and the extracellular domain of gpl30.
Cytokine-toxin conjugates:
Several applications of IL-6 inhibitors entail the elimination 35 of IL-6 dependent tumors, such as multiple myeloma. This goal can be achieved by the use of IL-6-toxin conjugate (Jean and
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Murphy, Prot. Eng. 4, 989, 1991). Malignant cells that have receptor for IL-6 would bind the toxin via the IL-6 portion of the conjugate and would be eliminated by toxin activity. Toxicity to all non-malignant cells that also express the IL-6 5 receptor is a dangerous possibility. Since IL-6 is required for development of normal humoral and cellular immune response, it is possible to speculate that treated patients would immunocompromised.
Peptide antagonists of IL-6
Grube and Cochran identified a regulatory domain of the IL-6 receptor (J. Biol. Chem. 269: 20791, 1994). The region is from the extramembranal domain of the IL-6R and it is involved in the regulation of IL-6 signal transmission. A synthetic 15 peptide, corresponding to residues 249-264 of the IL-6R
inhibits IL-6-dependent cell mitogenesis and IL-6-stimulated acute phase response without affecting ligand binding.
In a search for possible lead compounds, epitope mapping of the 20 human IL-6R was carried out (Halimi et al., Eur. Cytokin, Netw. 6:135, 1995) with mAbs to IL-6R which inhibit the biological activity of IL-6 (Novick, et al., Hybridoma 10, 137, 1991). The 10 mer linear peptides that were recognized by two of the -antibodies are from the same region identified by-Grube and. 25 Cochran (ibid). The peptides identified by these two groups are indicated in the frame of the IL-6R sequence in figure l.(* Grube and Cochran, ** Halimi et al.).
International PCT application WO 97/13781 discloses these 30 synthetic peptides and analogs derived from the IL-6 that inhibit IL-6 activity. The peptides claimed are characterized also by being a linear epitope recognized by one or more Mabs specific to IL-6R. Peptides 1122 and 1123 (Halimi et al. ibid), were synthesized and found to inhibit IL-6 bioactivity in vitro 35 with an ID50 of about 100 j^M.
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WO 00/72864 PCT/IL00/00305
International PCT application WO 95/13086 and US patent 5,420,109, discloses peptides which are cytokine restraining agents having the general formula: Xl-X2-His-DPhe-Arg-DTrp-X3. These peptides are non-specific agents which modulate the 5 activity of various cytokines (TNF, IL-1, IL-6 and IL-8)
simultaneously, and therefore are not specific IL-6 inhibitors.
International PCT application WO 97/48728, discloses synthetic peptides which derived from IL-6 and from IL-6 receptor (either 10 the IL-6R or gpl30), and have IL-6 antagonistic or agonistic activity. The peptides interact with the receptor site of IL-6 or with IL-6Rs present at target cells or when combined, interact with both sites (IL-6 and IL-6R).
US Patent No. 5,210,075 discloses IL-6 antagonist peptides of 15 varying length, which are modeled after a portion of the sequence of IL-6 itself (p51-70 Hirano et al. Nature 324:73, 1986), or which are modeled after four different portions of the sequence of the IL-6 receptor molecule.
None of these disclose conformationally constrained IL-6 peptide antagonists which are cyclized as described in the present invention.
Peptide mimetic and backbone cyclized peptide analog 25 antagonists of IL-6
It is most beneficial to produce conformationally constrained peptide analogs overcoming the drawbacks of the native peptide molecules (low metabolic stability, poor oral bio-availability, rapid liver and kidney excretion, and lack of selectivity), 30 thereby providing improved therapeutic properties.
A novel conceptual approach to the conformational constraint of peptides was introduced by Gilon, et al., (Biopolymers 31:745, 1991), who proposed backbone to backbone cyclization of 35 peptides. The theoretical advantages of this strategy include the ability to effect cyclization via the carbons or nitrogens of the peptide backbone without interfering with side chains
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that may be crucial for interaction with the specific receptor of a given peptide.
Further disclosure by Gilon and coworkers (WO 95/33765) 5 provided methods for producing building units required in the synthesis of backbone cyclized peptide analogs. Recently, The successful use of these methods to produce backbone cyclized peptide analogs having somatostatin activity was also disclosed (WO 98/04583 and WO 99/65508). Libraries of backbone cyclized 10 analogs including IL-6 analogs are disclosed in international application WO 97/09344. In that disclosure, a selection method termed "Cycloscan", based on conformationally constrained backbone cyclic peptide libraries that allows rapid detection of active analogs derived from a given sequence is described.
Nowhere in the background art, are backbone cyclized peptide analogs shown to possess IL-6 inhibitory activity.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide novel peptide analogs, which are characterized in that they incorporate building units with bridging groups attached to the alpha nitrogens of alpha amino acids, having IL-6 inhibitory activity. Specifically, these compounds are backbone cyclized 25 IL-6 antagonists comprising a peptide sequence of five to twenty amino acids that incorporates at least one building unit, said building unit containing one nitrogen atom of the peptide backbone connected to a bridging group comprising an amide, thioether, thioester or disulfide, wherein the at least 30 one building unit is connected via said bridging group to form a cyclic structure with a moiety selected from the group consisting of a second building unit, the side chain of an amino acid residue of the sequence or the N-terminal amino acid residue. Preferably, the peptide sequence incorporates six to 35 twelve amino acids, having IL-6 inhibitory activity.
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Bioactivity of IL-6 requires each of the molecules in the tripartite complex, i.e. IL-6, IL-6R and gpl30 signal transducer, to interact with the two other partners. The objectives of the present invention will be achieved by peptides that inhibit any one of interactions in the complex as follows:
a) Peptides derived from IL-6 that interfere with IL-6-IL-6R interaction or with IL-6/gpl30 interaction.
b) Peptides derived from IL-6R that interfere with IL-6-IL-6R interaction or with IL-6R/gpl30 interaction.
c) Peptides derived from gpl30 that interfere with IL-6/gpl30 or with IL-6R/gpl30 interactions.
According to one aspect of the present invention, the segment of the IL-6R spanning residues 247-271 is currently a most preferred embodiment for development of conformationally constrained backbone cyclized peptide analogs to be used as an inhibitor of IL-6 activity.
From the screening of backbone cyclized peptide analogs, preferred peptide analogs were unexpectedly found to have significantly enhanced inhibitory activity in comparison to the linear epitope. Some of these backbone cyclized peptide analogs mimic the IL-6R inhibitory domain of residues 249-258, others mimic the region in IL-6 which binds its receptor. But unlike the previously described peptides derived from these domains, these novel backbone cyclized peptide analogs possess unique features which make them more suitable for use in pharmaceutical compositions for treatment of pathological conditions associated with elevated levels of IL-6.
According to the present invention it is now disclosed that more preferred backbone cyclized analogs are decapeptide and nonapeptide antagonists of IL-6 with improved activity and metabolic stability. Additional more preferred analogs may advantageously include at least one D-isomer of amino acids in their sequence.
WO 00/72864 PCT/ILOO/00305
Preferably, the backbone cyclized analogs of the present invention are derived from, or mimic the sequence of the IL-6R molecule, preferably related to residues 247-271 of the IL-6R amino acids sequence. Additional preferred analogs are derived 5 from the sequence of the IL-6 molecule.
A preferred embodiment of the present invention has the following formula:
R2a9_R250_R251_R252_R253_NR254_R255_R256_R257_NR258_x
(CH2 ) m" Y2— (CH2 ) n J 15 Formula No. 1
wherein m and n are 1 to 5;
X designates a terminal carboxy acid, amide or alcohol group;
R249
is
Trp, (L) or (D)Lys, (L)
or (D) Tyr or (D)Phe;
R250
is. Arg;
r251
is
(L) or (D)Leu or Lys;
R252
is
(L) or (D)Arg;
R253
is
(D) - or (L) - Phe;
R254
is
Ala;
r255
is
(D)- or (L)— Leu or is
Lys;
R256
is absent or is (L) or (D)
Arg;
R257
is
(L) or (D) Tyr;
R258
is
Ala; and
Y2 is amide, thioether, thioester or disulfide.
A more preferred embodiment of the present invention has the following formula:
R249_R250_r251_r252_r253_nr254_r255_r256_r257_^r258_x
"-(CH2)m-Y2-(CH2)n Jl 40 Formula No. 2
wherein m and n are 1 to 5;
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X designates a terminal carboxy acid, amide or alcohol group;
R249
is
Trp, (D)Lys or (D)Phe;
r250
is
Arg;
R251
is
Ly§ or (D)Leu;
R252
is
(D)Arg;
r253
is
(D)- or (L)- Phe;
r254
is
Ala;
r255
is
(D)- or (L)- Leu;
R256
is absent or is Arg;
r257
is
(D) Tyr;
R258
is
Ala; and
Y2 is amide, thioether, thioester or disulfide.
Unconventional amino acids which abbreviated in the formulae are as defined hereinbelow.
The currently most preferred backbone cyclized IL-6 antagonists of the invention which are derived from the IL-6 receptor molecule are as follows:
Trp-Arg-Lys-(D)Arg-Phe-AlaC3-Leu-Arg-(D)Tyr-AlaN3-NH2 designated herein as PTR-5045
(D)Lys-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3-(D)Leu-Arg-(D)Tyr-AlaN3-NH2 designated herein as PTR-5041
(D)Phe-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3-Leu-(D)Tyr-AlaN3-NH2 designated herein as PTR-5043
These peptide analogs were found to inhibit the cytotoxic effect of IL-6 in various in-vitro bioassays. PTR 5045 was also 30 found to be active in-vivo in prevention of IL-6 induced pathology, and to be metabolically functional bio-stable.
According to another aspect of the present invention, additional preferred analogs are derived from the sequence of 35 the IL-6 molecule. According to the present invention the region of the IL-6 molecule spanning loop AB and helix D, is currently a most preferred embodiment for development of
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conformationally constrained backbone cyclized peptide analogs to be used as an inhibitor of IL-6 activity.
According to the present invention it is now disclosed that additional mor^ preferred backbone cyclized analogs are hexapeptides antagonists of IL-6 with improved activity and metabolic stability. Additional more preferred analogs may advantageously include at least one D-isomer of amino acids in their sequence.
A preferred embodiment of the present invention, relating to peptides derived from IL-6, has the following formula:
R^-.NR2 R3 R4 NR5—R6-X
(CH2)n-Y2~(CH2) J
Formula No. 3
wherein m and n are 1 to 5;
X designates a terminal carboxy acid, amide or alcohol group;
R1 is (D)Bip, Gin, Lys, Lys(ZCL) or Dab;
R2 is (D)Lys, Gly, Ala or Trp
R3 is Orn, 4PyrAla, (L) or (D)Dab, (D)Arg , Lys or Dpr; R4 is Lys, Lys(ZCL), Arg, Arg(Mtr) or (D)Glu;
R5 is Asn, Trp or (D)Ala;
R6 is Arg, (p-N02)Phe, (L)- or (D)- Trp, Gin, Abu or Glu; 30 and
Y2 is amide, thioether, thioester or disulfide.
Another preferred embodiment of the present invention, relating to peptides derived from IL-6, has the following formula:
40
NR1—NR2—R3—R4--NR5—R6-X
L(CH2)m-Y2— (CH2)nJ
Formula No. 4
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wherein m and n are 1 to 5;
X designates a terminal carboxy acid, amide or alcohol group;
R1 is (D)Phe or Lys;
R2 is (D)Git, Lys or (D)Bip;
R3 is Dpr, 4PyrAla or (L)- or (D)- Arg;
R4 is HomArg, Orn or Lys;
R5 is (D)Gln or (L)- or (D)- Trp;
R6 is (L)- or (D)- Gin or (p-N02)Phe; and 10 Y2 is amide, thioether, thioester or disulfide.
The currently most preferred backbone cyclized IL-6 antagonists of the invention which are derived from the IL-6 molecule are as follows:
(D)Bip-(D)LysC3-Orn-Lys-AsnN2-Arg-NH2 denoted 70003-20; (D)Bip-(D)LysC3-4PyrAla-Orn-TrpN2- (p-N02) Phe-NH2 denoted 70003-41;
(D)Bip-(D)LysC2-Lys-Lys(ZC1)-(D)TrpN2-Abu-NH2 denoted 70003-88; 20 Gln-GlyC2-(D)Dab-Arg(MTR)-TrpN2-Trp-NH2 denoted 70003-61;
Lys(ZCL)-GlyC2-Dab-(D)Glu-(D)AlaN3-(D)Trp-NH2 denoted 70003-57; (D)Bip-GlyC2-Dab-(D)Glu-(D)AlaN3-Abu-NH2 denoted 70003-91; Lys(ZCL)-AlaC2-Dab-(D)Glu-(D)AlaN3-(D)Trp-NH2 -denoted 70003-25; Lys-TrpC2-(D)Arg-Lys-TrpN3-Gln-NH2 denoted 70003-34; 25 Dab-TrpC2-Dpr-Arg(MTR)-(D)AlaN3-Glu-NH2 denoted 70003-83; (D)PheC2-(D)Cit-Dpr-HomArg-(D)GlnN2-(D)Gln-NH2 denoted 70003-17;
LysC3-Lys-4PyrAla-Orn-TrpN2-(p-N02)Phe-NH2 denoted 70003-40; LysC4-Lys-(D)Arg-Lys-TrpN3-Gln-NH2 denoted 70003-33; 30 (D)PheC2-(D)Bip-Arg-Lys-(D)TrpN2-Gln-NH2 denoted 70003-81.
Preferably, the backbone cyclized peptide analogs of the present invention incorporates two such Na-to-functionalized amino acid derivatives which may be linked to one another to 35 form N-backbone to N-backbone cyclic peptide analogs.
Additional preferred analogs of the invention can be
14
WO 00/72864 PCT/IL00/00305
constructed with two or more cyclizations, including N-backbone to N-backbone, as well as backbone to side-chain or any other peptide cyclization.
Backbone cyclized analogs of the present invention may be used as pharmaceutical compositions and in methods for the treatment of disorders including: cancers (including multiple myeloma/plasmacytoma), autoimmune diseases (including rheumatoid arthritis, multiple sclerosis, SLE and diabetes), 10 infectious diseases (bacterial and viral infection, septic shock), inflammatory diseases (including pancreatitis), immune deficiency diseases (including AIDS), hematologic diseases (e.g., leukemia, lymphoma), allergic diseases, organ transplantation reactions, Castelman's disease, Lennart's 15 T-cell lymphoma, Non-Hodgkin's lymphoma, Cardiac myxoma,
mesangial proliferative glomerulonephritis, polyclonal B-cell activation conditions, abnormal acute phase protein production conditions.
The pharmaceutical compositions comprising pharmacologically active backbone cyclized IL-6 antagonist and a pharmaceutically acceptable carrier or diluent represent another embodiment of . the invention, as do the methods for the treatment of a mammal in need thereof with a pharmaceutical composition comprising an 25 effective amount of an IL-6 antagonist according to the invention. Methods of treatment using the compositions of the invention are useful for therapy of cancers (including multiple myeloma/plasmacytoma), autoimmune diseases (including rheumatoid arthritis, multiple sclerosis, SLE and diabetes), 30 infectious diseases (bacterial and viral infection, septic shock), inflammatory diseases (including pancreatitis), immune deficiency diseases (including AIDS), hematologic diseases (e.g., plasma cell dyscrasias, leukemia, lymphoma), allergic diseases, organ transplantation reactions, Castelman's disease, 35 Lennart's T-cell lymphoma, Non-Hodgkin's lymphoma, Cardiac myxoma, mesangial proliferative glomerulonephritis, polyclonal
WO 00/72864 PCT/IL00/00305
B-cell activation conditions, abnormal acute phase protein production conditions, and osteoporosis using such compositions. The pharmaceutical compositions according to the present invention advantageously comprise at least one backbone 5 cyclized peptide analog which includes at least one D-isomer of amino acids in its sequence. These pharmaceutical compositions may be administered by any suitable route of administration, including topically or systemically. Preferred modes of administration include but are not limited to parenteral routes 10 such as intravenous and intramuscular injections, as well as via nasal or oral ingestion.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a schematic drawing depicting known active IL-6 inhibitory and non-active peptides derived from the IL-6R.
Figure 2 describes the effect of backbone cyclic peptide 20 analogs on B16.F10.9 melanoma cells growth.
Figure 3 describes in-vivo effects of IL-6 antagonists on IL-6 mediated acute-phase responses: a) IL-6 serum levels, b) fibrinogen pla.sma_l.evels and c) changes in body weight, in 25 normal and IL-6 knockout mice.
Figure 4 is a chart describing the biological activity and selectivity of backbone cyclized peptide antagonists of IL-6, in TF1 cells maintained with IL-6 or GM-CSF.
DETAILED DESCRIPTION OF THE INVENTION
Definitions:
The compounds herein described may have asymmetric centers. ' All chiral, diastereomeric, and racemic forms are included in the present invention. Many geometric isomers of olefins and
16
WO 00/72864 PCT/ILOO/00305
the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention.
By "stable compound" or "stable structure" is meant herein a 5 compound that i,s sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.
As used herein and in the claims, the phrase "therapeutically 10 effective amount" means that amount of novel backbone cyclic peptide analog or composition comprising same to administer to a host to achieve the desired results for the indications described herein, such as but not limited of inflammation, cancer, endocrine disorders and gastrointestinal disorders.
The term, "substituted" as used herein, means that any one or more hydrogen atoms on the designated moiety is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the 20 substitution results in a stable compound.
When any variable (for example R, X, Z, etc.) occurs more than one time in any constituent or in any Formula herein, its definition on each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents • 25 and/or variables are permissible only if such combinations result in stable compounds.
As used herein "peptide" indicates a sequence of amino acids linked by peptide bonds. The IL-6 peptide antagonists of this 30 invention comprise a sequence of amino acids of 4 to 24 amino acid residues, preferably 6 to 16 residues, each residue being characterized by having an amino and a carboxy terminus.
A "building unit" indicates an Na derivatized a amino acid of 35 the general Formula No. 5:
17
PCT/IL00/OO3O5
-N-CH (R') -CO-
X
Formula No. 5
wherein X is a spacer group selected from the group consisting 15 of alkylene, substituted alkylene, arylene, cycloalkylene and substituted cycloalkylene; R1 is an amino acid side chain, optionally bound with a specific protecting group; and G is a functional group selected from the group consisting of amines, thiols, alcohols, carboxylic acids and esters, and alkyl 20 halides; which is incorporated into the peptide sequence and subsequently selectively cyclized via the functional group G with one of the side chains of the amino acids in said peptide sequence or with another co-functionalized amino acid derivative.
The methodology for producing the building units is described in US Patent No. 5,883,293 and International Patent Applications WO 95/33765 and WO 98/04583, both of which are expressly incorporated herein by reference thereto for further details of this methodology. The building units are abbreviated by the three letter code of the corresponding modified amino acid followed by the type of reactive group (N for amine, C for carboxyl), and an indication of the number of spacing methylene groups. For example, GlyC2 describes a modified Gly residue with a carboxyl reactive group and a two carbon methylene 35 spacer, and PheN3 designates a modified phenylalanine group with an amino reactive group and a three carbon methylene spacer.
As used herein "backbone cyclic peptide" or "backbone cyclized 40 peptide" denotes an analog of a linear peptide which contains at least one building unit that has been liked to form a bridge
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WO 00/72864 PCT/ILOO/00305
via the alpha nitrogen of the peptide backbone to another building unit, or to another amino acid in the sequence.
As used herein a "PTR" number denotes a reference number 5 assigned to a backbone cyclic peptide analog that is synthesized, purified and fully characterized (e.g., by HPLC, MS, capillary electrophoresis, by amino acid analysis for peptide content and amino acid ratio determination).
As used herein and in the claims, in the formulae of the more preferred backbone cyclic peptide analogs, the superscript numbers following the amino acids refer to their position numbers in the native IL-6 receptor or in the IL-6 molecule.
Abbreviations:
Certain abbreviations are used herein to describe this invention and the manner of making and using it.
For instance, AcOH refers to acetic acid, Ada refers to adamantanacetyl, Adac refers to adamantanecarbonyl, Alloc refer 20 to allyloxycarbonyl, AIDS refers to acquired immune deficiency syndrome, Boc refers to the t-butyloxycarbonyl radical, BOP refers to benzotriazol-l-yloxy-tris-(dimethylamino)phosphonium hexafluorophosphate, BSA refers to bovine serum, albumin, Cbz refers to the carbobenzyloxy radical, CNTF refers to ciliary 25 neurotrophic factor, DCC refers to dicyclohexylcarbo.diimide, DCM refers to Dichloromethane, Dde refers to
1-(4,4-dimethyl2,6-dioxocyclohex-l-ylidene-ethyl), DIEA refers to diisopropyl-ethyl amine, DMF refers to dimethyl formamide, DPPA refers to diphenylphosphoryl azide, Dtc refers to 30 5,5-dimethylthiazolidine-4-carboxylic'acid, EDT refers to ethanedithiol, ESI-MS refers to electrospray ionization mass spectrometry, Fmoc refers to the fluorenylmethoxycarbonyl radical, HBTU refers to
1-hydroxybenztriazolyltetramethyl-uronium hexafluorophosphate, 35 HF refers to hydrofluoric acid, HOBT refers to
1-hydroxybenzotriazole, HPLC refers to high pressure liquid chromatography, IL-1 refers to interleukin-1, IL-6 refers to
19
WO 00/72864 PCT/IL0O/OO3O5
interleukin-6, IL-6R refers to interleukin-6 receptor, IL-11 refers to interleukin-11, KS refers to Kaposi's sarcoma, LC-MS refers to liquid chromatography mass spectrometry, LIF refers to leukocyte inhibitory factor, LIF-R refers to leukocyte inhibitory factor receptor, LPS refers to lipopolysacaride, mAb refers to monoclonal antibody, MMPs refers to Matrix Metalloproteinases, MPS refers to multiple parallel synthesis, MS refers to mass spectrometry, NMM refers to
N-methylmorpholine, NMP refers to l-methyl-2-pyrolidonone, OSM refers to oncostatin M, PyBOP refers to Benzotriazole-l-yl-oxy-tris-pyrrolidino-phosphonium hexafluorophosphate, PyBrOP refers to Bromo-tris-pyrrolidino-phosphonium hexafluorophosphate, RA refers to Rheumatoid arthritis, RP refers to reverse phase, SLE refers to system lupus ethrythematosus, TBTU refers to 2-(lH-benzotriazole-l-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate, tBu refers to the tertiary butyl radical, TFA refers to trifluoroacetic acid, TIS refers to tri-isopropyl-silane.
The amino acids used in this invention are those which are available commercially or are available by routine synthetic methods.. Certain residues may require special methods for incorporation into the peptide, and either sequential,
divergent and convergent synthetic approaches to the peptide sequence are useful in this invention. Natural coded amino acids and their derivatives are represented by three-letter codes according to IUPAC conventions. When there is no indication, the L isomer was used. The D isomers are indicated by "D" before the residue abbreviation. List of Non-coded amino acids: Abu refers to 2-aminobutyric acid, Aib refers to 2-amino-isobutyric acid, p-Ala refers to p-Alanine, Bip refers to Beta-(4-biphenyl)-alanine, Cit referes to citruline, Dab refers to Diaminobutyric acid, Dpr refers to diaminopropionic acid, HomArg refers to homo arginine, Hcys refer to homocystein, Lys(ZCl) refers to Lys with e-amino group
WO 00/72864 PCT/IL00/00305
protected by benzyl chloride, INal refers to 1-naphthylalanine, 2Nal refers to 2-naphtylalanine, Nva refers to norvaline,, (p-Cl)Phe refers to para chloro Phenylalanine, (p-NH2)Phe refers to para amino Phenylalanine, (p-F)Phe refers to para fluoro Phenylalanine, (P-NO2) Phe refers to para nitro Phenylalanine, 4PyrAla refers to 4-Pyridylalanine, Thi refers to thienylalanine.
As described earlier, IL-6 plays a pivotal role in mediating immune responses, acute-phase reactions and hematopoiesis. However, it has been shown that the loss of IL-6 regulation, or its overexpression, may be involved in a number of pathological conditions. Specifically, elevated IL-6 levels are detected in 15 bacterial, parasite and viral infections, including HIV, as well as in chronic autoimmune disorders such as rheumatoid arthritis, systemic lupus erythematosus, psoriasis, and multiple sclerosis. In addition, IL-6 is implicated in the pathology of various neoplasms, such as multiple myeloma, 20 leukemia, Kaposi's sarcoma, renal cell carcinoma and cardiac myxoma. In particular, IL-6 has been recognized as the major cytokine required for growth of multiple myeloma tumors and is also possibly involved in the n tumor-associated toxicity in multiple myeloma patients.
It is expected that peptides which inhibit IL-6 function will have broad therapeutic,utility in many mammalian diseases. Therapeutic use of backbone cyclized IL-6 peptide antagonists 30 of the present invention is expected to be beneficial in treating a variety of IL-6 associated diseases, many of which are currently treated with immunomodulators or immunosuppresants.
Such IL-6 associated diseases include:
a) Multiple myeloma/plasmacytoma.
b) Autoimmune diseased (including, but not limiting to,
rheumatoid arthritis, multiple sclerosis, SLE and diabetes).
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WO 00/72864 PCT/1LOO/00305
c) Infection diseases (bacterial and viral infection, septic d e f g
h i j
k 1 m n o P
shock).
Inflammatory diseases.
Immune deficiency diseases, including AIDS. Hematologic, diseases (e.g., plasma cell dyscrasias, leukemia, lymphoma).
Allergic diseases.
Organ transplantation reactions.
Castelman's disease.
Lennart's T-cell lymphoma Non-Hodgkin's lymphoma.
Cardiac myxoma.
Mesangial proliferative glomerulonephritis. Polyclonal B-cell activation conditions.
Abnormal acute phase protein production conditions. Osteoporosis
By way of exemplification of the principles of the present invention, a search for inhibitory peptides was focused on the IL-6R/gpl30 interface. This was followed by an investigation of the IL-6/IL-6R and the IL-6R/gpl30 interfaces. According to one presently preferred embodiment the search comprises mainly rational design and combinatorial libraries screening .using multiple parallel synthesis (MPS) approaches.
The advantages of backbone cyclic peptides over, existing and previously suggested therapies of multiple myeloma, are as follows:
The suggested IL-6 inhibitor is non-cytotoxic as compared with the currently utilized cytotoxic drugs. The effect of the IL-6 antagonist would be specific to multiple myeloma cells and a small subset of IL-6 dependent cells, where the other cytotoxic drugs are non-selective and kill all types of dividing cells in the body.
The suggested IL-6 antagonist is small and thus non-immunogenic by nature, as compared to the potentially immunogenic antibodies, antibody fragments and minibodies.
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WO 00/72864 PCT/IL00/00305
The suggested IL-6 antagonist could be modified to be orally bioavailable. It is unlikely that proteins (antibodies, fragments or minibodies) would be orally available.
Over 7400 individual backbone cyclized peptide analogs were synthesized in MPS format and tested by at least one type of bioassay for inhibition of IL-6 bioactivity.
The best peptides achieved at this screening stage,
demonstrated an estimated IC50 around 1 ^M. This represents 10 10 to 100 fold improvement of peptide analogs available as linear peptides derived from the IL-6R molecule.
About 50 peptide analogs (PTRs), chosen by activity from the MPS syntheses, were synthesized in large scale, purified and fully characterized. These PTRs were tested for IL-6 inhibitory 15 activity in at least one in-vitro bioassay.
From the above described massive screening of backbone cyclized peptide analogs in MPS and PTR format three peptides were unexpectedly found as particularly active. These backbone cyclized peptide analogs mimic the IL-6R inhibitory domain of 20 residues 249-258, and the region in IL-6 which binds to the receptor. But unlike the previously described peptides derived from these domains, these novel backbone cyclized peptide analogs possess unique features which make them more suitable for use in pharmaceutical compositions for treatment of 2.5 pathological conditions associated with elevated levels of - IL-6.
The preferred backbone cyclized IL-6 antagonists of the present invention are now described.
One embodiment has the following formula:
r249_r250_r251_r252_r253_nr254_r255_r256_r257_nr258_x
-(CH2)m— Y2— (CH2)n J Formula No. 1
23
WO 00/72864 PCT/ILOO/00305
wherein m and n are 1 to 5;
X designates a terminal carboxy acid, amide or alcohol group;
R249
is
Trp, (L) or (D)Lys, (L)
or (D) Tyr or (D)Phe;
r250
is
Arg,;
R251
is
(L) or (D)Leu or Lys;
R252
is
(L) or (D)Arg;
R253
is
(D)- or (L)- Phe;
R254
is
Ala;
R255
is
(D)- or (L)- Leu or is
Lys;
R256
is absent or is (L) or (D)
Arg;
R257
is
(L) or (D) Tyr;
R258
is
Ala; and
Y2 is amide, thioether, thioester or disulfide.
A currently more preferred embodiment has the following formula:
R249_R250_R251_R252_R253_NR254_R255_R256_R257_NR258_X
- (CH2)m-Y2- (CH2)n J Formula No. 2
wherein m and- n are .1. to. 5;
X designates a terminal carboxy acid, amide or alcohol group;
R249 is Trp, (D) Lys or (D)Phe;
R250 is Arg;
R251 is Lys or (D)Leu;
R252 is (D)Arg;
R253 is (D)- or (L)- Phe;
R254 is Ala;
R255 is (D)- or (L)- Leu;
256
R is absent or is Arg;
R257 is (D) Tyr;
R258 is Ala; and
Y2 is amide, thioether, thioester or disulfide.
24
PCT/ILOO/00305
A most preferred compound according to this embodiment is denoted PTR 5045 wherein the residues are as follows:
R249
is
Trp;
r25°
is
Arg,;
R251
is
Lys;
r252
is
(D)Arg;
R253
is
Phe;
R254
is
Ala;
R255
is
Leu;
R256
is
Arg;
R257
is
(D)Tyr;
r25B
is
Ala; and
Y2 is amide.
Another preferred compound according to this embodiment is denoted PTR 5041 wherein the residues are as follows:
r249
is
(D)Lys;
R250
is
Arg;
R251
is
{D)Leu;
R252
is
(D)Arg;
r253
is
(D)Phe;
R254
is
Ala;
R255
is
Leu;
R256
is
Arg;
R257
is
(D) Tyr;
R258
is
Ala; and
Y2 is amide.
Another preferred compound according to this embodiment is denoted PTR 5043 wherein the residues are as follows:
R249
is
(D)Phe;
R250
is
Arg;
R251
is
(D)Leu;
R252
is
(D)Arg;
R253
is
(D)Phe;
R254
is
Ala;
WO 00/72864 PCT/ILOO/00305
R265 is Leu;
R256 is absent;
R257 is (D) Tyr;
R258 is Ala; and Y2 is amide.
Another preferred embodiment of the present invention, relating to peptides derived from IL-6, has the following formula:
R1 NR2 R3 R4 NR5—RS-K
(CH2)m-Y2—(CH2)n J
Formula No. 3
wherein m and n are 1 to 5;
X designates a terminal carboxy acid, amide or alcohol group;
R1 is (D)Bip, Gin, Lys, Lys(ZCL) or Dab;
R2 is (D)Lys, Gly, Ala or Trp
R3 is Orn, 4PyrAla, (L) or (D)Dab, (D)Arg , Lys or Dpr; R4 is Lys, Lys(ZCL), Arg, Arg(Mtr) or (D)Glu;
R5 is Asn, Trp or (D)Ala;
R6 is Arg, (p-N02)Phe, (L)- or (D)- Trp, Gin, Abu or Glu;
and
Y2 is amide, thioether, thioes-ter or disulfide.
Another preferred embodiment-of the present invention, relating 30 to peptides derived from IL-6, has the following formula:
NR1—NR2 R3 R4—NR5—R6-X
L (CH2)m-Y=— (CH2)n J
Formula No. 4
wherein m and n are 1 to 5;
40 X designates a terminal carboxy acid, amide or alcohol group;
R1 is (D)Phe or Lys;
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WO 00/72864 PCT/ILO0/Q0305
R is (D)Cit, Lys or (D)Bip;
R3 is Dpr, 4PyrAla or (L)- or (D)- Arg;
R4 is HomArg, Orn or Lys;
R5 is (D)Gin or (L)- or (D)- Trp;
R6 is (L) - ,or (D)- Gin or (p-N02)Phe; and
Y2 is amide, thioether, thioester or disulfide.
The most preferred backbone cyclized IL-6 antagonists of the invention described in table 1:
Table 1: The most preferred analogs of the invention.
PTR 5045
Trp-Arg-Lys-(D)Arg-Phe-AlaC3-Leu-Arg-(D)Tyr-AlaN3-X
PTR 5041
(D)Lys-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3-(D)Leu-Arg-(D)Tyr-AlaN3-X
PTR 5043
(D)Phe-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3~Leu-(D)Tyr-AlaN3-X
70003-20
(D)Bip-(D)LysC3-Orn-Lys-AsnN2-Arg-X
70003-41
(D)Bip-(D)LysC3-4PyrAla-Orn-TrpN2-(p-N02) Phe-X
70003-88
(D)Bip-(D)LysC2-Lys-Lys(ZCl)-(D)TrpN2-Abu-NH2
70003-61
Gln-GlyC2-(D)Dab-Arg(MTR)-TrpN2-Trp-X
70003-57
Lys(ZCL)-GlyC2-Dab-(D)Glu-(D)AlaN3-(D)Trp-NH2
70003-91
(D)Bip-GlyC2-Dab-(D)Glu-(D)AlaN3-Abu-NH2
70003-25
Lys(ZCL)-AlaC2-Dab-(D)Glu-(D)AlaN3-DTrp-X
70003-34
Lys-TrpC2-(D)Arg-Lys-TrpN3-Gln-X
70003-83
Dab-TrpC2-Dpr-Arg(MTR)-(D)AlaN3-Glu-X
70003-17
(D)PheC2-(D)Cit-Dpr-HomArg-(D)GlnN2-(D)Gln-X
70003-40
LysC3-Lys-4PyrAla-Orn-TrpN2-(p-N02)Phe-X
70003-33
LysC4-Lys-(D)Arg-Lys-TrpN3-Gln-NH2
70003-81
(D)PheC2-(D)Bip-Arg-Lys-(D) TrpN2-Gln-X
where X is -NH2 or -OH and the bridging group extends between the two building units.
A more preferred embodiment of the invention incorporates two Na-(o-functionalized amino acid derivatives which may be linked to one another to form N-backbone to N-backbone cyclic peptide analogs.
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WO 00/72864 PCT/ILOO/00305
The most striking advantages of backbone cyclization are:
1) Cyclization of the peptide sequence is achieved without compromising any of the side chains of the peptide thereby decreasing the chances of sacrificing functional groups essential for biological recognition and function.
2) Optimization of the peptide conformation is achieved by allowing permutation of the bridge length, direction, and bond type (e.g., amide, disulfide, thioether, thioester, etc.) and position of the bond in the ring.
3) When applied to cyclization of linear peptides of known activity, the bridge can be designed in such a way as to minimize interaction with the active region of the peptide and its cognate receptor. This decreases the chances of the cyclization arm interfering with recognition and function, and also creates a site suitable for attachment of tags such as radioactive tracers, cytotoxic drugs, light capturing substances, or any other desired label.
Peptide analogs can be constructed with two or more cyclizations, including N-backbone to N-backbone, as well as backbone to side-chain or any other peptide,cyclization. The second cyclization, can be formed by incorporating at least one additional building unit into a peptide sequence and linking it to another building unit, to the amino acid side chain or to. any of the peptide terminals. In addition the second cyclization can be a side-chain to side-chain (including di-sulfide bond), or a side-chain to terminal cyclization.
It has now unexpectedly been found that the backbone cyclized IL-6 antagonists of the present invention which were identified by screening of individual backbone cyclized peptide analogs that were synthesized and assayed for inhibition of IL-6 activity, are 10-100 folds more active than the linear IL-6 inhibitory peptides previously described.
The backbone cyclic peptides of this invention are novel analogs which mimic the IL-6R inhibitory domain of residues
28
WO 00/72864 PCT/ILOO/00305
249-258. The amino acid sequence of the backbone cyclic analogs is based on what was identified as the most active inhibitory fragment of the IL-6R (Grube and Cochran, ibid). Additional analogs mimic a non-continuos region of the IL-6 molecule, comprising the ,contact residue of IL-6 to its receptor. These analogs have an additional advantage of having molecular weights of around 1000 dalton.
The present innovative backbone cyclic analogs preferably include 5 to 20 amino acids with special amino acid modifications. Specifically, at least one amino acid in each analog is a D-isomer of the amino acid.
The special feature of the novel backbone cyclic peptide analogs is their metabolic stability as tested in vitro against degradation of the most aggressive enzyme mixture in the body (e.g., renal homogenate). PTR 5045 is stable under these conditions for up to 24 hours. The previously described peptide analogs derived from the IL-6R, and fragments of the native protein, are significantly less stable metabolically.
General method for synthesis, purification and characterization of backbone cyclic peptides.
Synthesis:
Resin: 1 g Rink amide or Tenta-gel resin, with loading of
0.2.0.7 mmol/gr.
Fmoc-deprotection performed with 7 mL of 20% piperidine in NMP. Twice for 15 minutes following 5 washes with 10 ml NMP for 2 minutes with shaking.
Couplings:
1. Regular couplings (coupling to simple amino acids): with a solution containing 3 equivalents amino acid, 3 equivalents PyBroP and 6 equivalents of DIEA in 7 ml NMP. For 0.5-2 hours with shaking. Coupling is monitored by ninhydrine test and repeated until the ninhydrine solution become yellow.
2. Coupling of His and Asn with a solution containing 5 equivalents DIC and 5 equivalents HOBT in 10 ml DMF.
29
WO 00/72864 PCT/IL0O/OO3O5
3. Coupling to Gly building units: with a solution containing 3 equivalents amino acid, 3 equivalents PyBroP and 6 equivalents DIEA in 7 ml NMP. Twice for 1-4 hours with shaking.
4. Coupling to building units which are not Gly: with a solution containing 5 equivalents amino acid, 1.5 equivalents triphosgene and 13 equivalents collidine in 15 ml dioxane or THF. Twice for 0.5-2 hours at 50°C with shaking.
Removal of the Allyl and Alloc protecting groups of the building units performed with 1.5 equivalents per peptide of Pd(PPh3)4 in 30 ml DCM containing 5% acetic acid and 2.5% NMM. For 1-4 hours with shaking.
Cyclization performed with a solution containing 3 equivalents PyBOP and 6 equivalents DIEA in 7 ml NMP. For 0.5-2 hours with shaking. Cyclization is monitored by ninhydrine test and repeated if necessary.
Cleavage performed using 82%-95% TFA supplemented with scavengers: 1-15% H2O, 1-5% TIS and 1-5% EDT.
Purification:
An individual purification method for each backbone cyclic peptide is developed on analytical HPLC to give the maximum isolation of the cyclic peptide from other crude components. The analytical method is usually performed using a C-18 Vydac column 250X4.6 mm as the stationary phase and water/ACN containing 0.1% TFA mixture gradient.
The preparative method is designed by implying the analytical separation method on the 2" C-18 Vydac preparative method. _ During the purification process, the peak containing the cyclic peptide is collected using a semi-automated fraction collector. The collected fractions are injected to the analytical HPLC for purity check. The pure fractions are combined and lyophilized.
Characterization:
The combined pure lyophilized material is analyzed for purity by HPLC, MS and capillary electrophoresis and by amino acid analysis for peptide content and amino acid ratio determination.
WO 00/72864 PCT/IL00/00305
General method for synthesis, purification and characterization and screening of backbone cyclic peptides in MPS format.
The MPS procedure is used as the routine peptide development procedure. Individual peptides, or groups of a few peptides, 5 are synthesized, in 96-wells microtiter plates equipped with filters that allow passage of solvent but not of solid phase matrix. A simple and efficient valve apparatus that enables simultaneous closing and opening of all the valves (produced by Millipore) is used. The system utilizes an approach in which 10 each well is equipped with a solvent permeable membrane at the bottom that does not allow passage of particles above a certain size. The process allows one to place resin in the wells, perform reaction in solvent, and remove the solvent from all the wells simultaneously by applying vacuum. These special 15 plates, which are available in the standard 96 well format allow the parallel synthesis of 96 peptides simultaneously. The synthesis scale of the procedure is in the range of 1-5 j^mole per well. Following purification by C18 reverse phase columns (SepPak purification), which is also carried in the standard 96 20 well format, the peptides are routinely dissolved in 1 ml of water to yield a theoretical crude concentration of 1-5 mM (depending on synthesis scale). Monitoring of chemical quality of the resulting peptides is performed by ESI-MS analysis. Analysis of several plates prepared on different occasions by 25 different operators indicated a general success rate of about 80% as judged by the presence of the desired peptide mass in the crude preparation. Further analysis of a peptides from MPS is carried out by LC-MS. The analysis revealed crude peptide quality similar to crude preparations of peptides synthesized 30 individually in large scale. Different steps or the complete process are now performed automatically using automatic peptide synthesizers. Peptides are tested for bioactivity at a dilution of 1:40 (theoretical crude concentration of 125 ^M), or higher, which apparently eliminated most of the toxic effects and 35 enabled routine biological testing of peptides.
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Detailed procedure for synthesis in MPS format:
For capacity of 5 j^mole 10 mg resin with a substitution of 0.5 mmol/gr is used.
Fmoc deprotection: To each well 100 jj.1 of 20% piperidine in NMP are added. The reaction shacked for 15 min. The NMP is removed by suction.
Washing after Fmoc deprotection: the resin is washed by placing 150 ^1 NMP into each well followed by evacuation of the solution by vacuum. This process is repeated 4 times.
Coupling using PyBroP:
Well capacity: 5 j^mol
Amount of amino acid per coupling per well: 2 6 jj,mol
Amino acid in NMP concentration: 650 mM
Amino acid volume used: 40 |al
PyBroP amount: 26 jjmol
PyBroP concentration: 403 mg/ml
PyBroP volume used: 30 ^,1
DIEA added: 10 ^1
Total reaction volume: 80 ^1
The amino acids are added to the pre-activation plate, then a fresh solution of PyBroP is distributed into this plate followed by addition of DIEA. The solution from this plate is transferred to the reaction plate and shacked for 1 hour. This coupling is repeated twice. -
Coupling using Mukayama reagent:
Amino acid solution at 650 mM - 40 jil Mukayama reagent at 111 mg/ml- 60 |xl Collidine added per well- 15 j^l
The same procedure as for coupling with PyBroP. Reaction temperature 50°C, reaction time: first coupling 4h, second coupling 16h,
Allyl Alloc deprotection: this step is performed after completing the assembly, by addition of 180 |jl solution of 1.5 g Pd(PPh3)4 in 20 ml CH2CI2 containing 5% AcOH + 2.5% NMM.
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Cyclization- this step is performed by addition of 100 ^1 solution of PyBoP in NMP + DIEA.
Cleavage of the peptide from the resin and SepPak purification:
After final Fmoc deprotection the resin is transferred into a
deep well micrdtiter plate, to each well 300 ^,1 of TFA solution containing 2.5% TIS, 2.5% H2O, 2.5% EDT are added. Removal of the TFA is performede by lyophilization. After cleavage the peptides are purified by SepPak.
Screening of IL-6 antagonists for biological activity.
In-vitro bioassays
Screening for bioactivity of potential IL-6 inhibitory peptides was performed in vitro. Inhibition of IL-6 results in the" death of IL-6 dependent cell lines such as the murine T1165 and B9, 15 or the human TF1 and XG1. Alternatively, inhibition of IL-6 can be monitored by following the IL-6 induced differentiation of A375, B16.F10.9 and Ml cells which results in continued growth of the cells. Measuring IgG secretion by CESS cell line can also be used for monitoring IL-6 inhibitory activity.
Five types of in vitro bioassays for IL-6 inhibition using different murine and human cell lines were used in different stages of the search, for screening of inhibitory peptides. Bioassay using B9 cells
B9 (murine myeloma) cells require IL-6 for growth. Inhibition 25 of IL-6 results in cell death. The assay procedure was performed as described in Halimi et al. (ibid).
Bioassay using T1165 cells
T1165 (murine myeloma cells) require IL-6 for growth and die if IL-6 is omitted or inhibited. The validity of the assay was 30 demonstrated by inhibition of IL-6 bioactivity using rabbit IL-6 antiserum.
Bioassay using B16.F10.9 melanoma cells
The F10.9 sub-line of B16 (murine melanoma) expresses gpl30 but not IL-6R. Addition of human IL-6 and human IL-6R, or a chimera 35 of IL-6/IL-6R results in differentiation which is associated with growth arrest of the cells. Inhibition of IL-6 results in
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continued growth. Since the end point of this assay is cell growth rather than cell death, this assay system was used primarily in order to differentiate between suspected toxic effects observed on B9 or T1165 cells, and true inhibition of IL-6 activity.
The B16.F10.9 cell assay was routinely used as a confirmation assay for the T1165 or TF1 assay which were the primary screening assays (at different stages of the search).
Evaluation of the results in this assay is possible using two methods. One method uses vital dyes for monitoring cell growth. The second method comprises visual observation of the cell morphology and establishing a cut off point based on the following observations:
Cells which are not treated with IL-6 create a monolayer that covers almost all the surface area. Treatment with IL-6 causes growth arrest and a morphological change: the cells become very narrow and elongated as compared to the more spread out shape of the non-treated cells. Treatment of the cells with IL-6 and an inhibitory peptide apparently completely restores cell growth but does not completely restores the cell morphology. Treatment of cells with IL-6 and a non-inhibitory peptide results in cells that appear to be very similar to the IL-6 treated cells.
Based on such observations, the results of the assay are reported as the last concentration of the peptide thai: cause almost complete inhibition of the effect of IL-6.
Bioassay using A375 cells
The A375 are human melanoma cells. IL-6 induces differentiation of A375 cells which is associated with growth arrest similar to the phenomenon observed with the B16F10.9 murine melanoma cells. Thus, inhibition of IL-6 results in continued growth of the cells which is easily quantifiable. In such case toxicity of peptides would register as a false negative rather than false positive. This conditions is preferable during screening process. Second, since these are human cells, the molecules involved in the bio-response, i.e. IL-6, IL-6R and gpl30 are all of human origin thus ensuring authenticity of the tested
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peptide bioactivity. Another advantage of the A375 cells is their ability to be induced by other cytokines that share the gpl30 signal transducer, i.e. leukemia inhibitory factor (LIF) and oncostatine M (OSM). As can be seen in table 2, LIF alone 5 does not affect A375 cells, unless the respective receptor (LIF-R) is also added. Apparently the A375 line we use lacks LIF-R. OSM is highly effective alone. The availability of this assay system, allows us to test, the specificity of our IL-6 inhibitory peptides vs. other cytokines of the family, in an 10 array of assays all using a single cell line. Assay performance is described in Savino et al. (ibid).
Table 2: Inhibition of A375 by cytokines other than IL-6
Cytokine
Concentration (ng/ml)
% Inhibition (relative to IL-6)*
LIF
1
1
LIF
2
LIF + LIFR
45
OSM
1
94
OSM
141
* The maximal (plateau) inhibitory activity of IL-6 on A375 15 cells was taken as 100%
The assay was validated using rabbit IL-6 antiserum which was used to inhibit"the bioactivity of IL-6. Testing of crude peptide- preparations, as well as high concentrations of purified peptides resulted in marked toxicity to the cells. 20 Further results indicated that the toxicity is dose dependent and decreases with increasing dilution of the crude peptide preparation, or at low concentration of the purified peptides. It is therefore anticipated that the assay can be used for screening of analogs with nM activity. It can be also used for 25 specifically screening for demonstration of peptide selectivity in the context of gpl30 related cytokines in order to differentiate between peptides that inhibit IL-6 alone and peptides that inhibit IL-6 and additional, gpl30 using cytokines.
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Bioassay using TF1 cells
TF1 cells (human erythroleukemia) cells require IL-6 for growth and thus inhibition of IL-6 bioactivity results in cell death, similar to T1165 cells. The origin of all relevant molecules is 5 human.
The problem associated with toxicity (false positive results) , could be overcome in the TF1 based assay since these cells can be induced by additional cytokines which are unrelated to IL-6 (not using the gpl30 signal transducer). It is possible to 10 induce the cells to grow with IL-6 and with additional cytokine e.g. GM-CSF. Specific inhibition of IL-6 bioactivity is therefore expected to register only in cells induced by IL-6 and not with GM-CSF. Validity of the use of TF1 cells and of the differential inhibition concept was demonstrated by the use 15. of rabbit IL-6 antiserum. Only the IL-6 induced growth was inhibited by the antiserum. Assay procedure is based on the procedure described in Fourcin et al. (ibid). The amount of viable cells at the end of the assay is determined by staining the cells with WST reagent as well as by measuring thymidine 20 corporation (3H-T) .
Inhibition of the IL-6 using peptides derived from the IL-6R or from gpl30, but not from the IL-6 itself could result in inhibition of other cytokines that also .utilize the gpl30 25 signal transduction system. In order to test the specificity of the peptide analogs in that respect, bioassays for the bioactivity of some of the other cytokines in the groups (i.e. IL-11, CNTF, OSM), are performed.
In-vitro binding assays
Binding assays are intended to measure the direct effect of the peptide on formation of the IL-6 active hexamer. Unlike the bioassays, the use of this assay could clearly demonstrate the mode of activity of the tested peptides. A simple format for 35 such assay would be as follows: IL-6, IL-6R and soluble gpl30 would be mixed in solution together with the test peptide. Capture of the putative hexamer would be achieved by an
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anti-gpl30 antibody and detection of the bound complex would be achieved by antibody to either IL-6 or IL-6R. A separate assay performed in order to test the interference of the peptide in the IL-6/IL-6R interaction.
Assays of similar format are used for testing the inhibition specificity of the peptide to the IL-6 bioactive complex by replacing the IL-6-IL-6R complex with commercially available cytokines and receptors of the other cytokines known to utilize 10 the gpl30 signal transducer.
In-vivo Assays
The prime clinical target for the IL-6 antagonist is multiple myeloma. In-vivo model systems are performed in mice inoculated 15 with murine IL-6 dependent myeloma cell lines. Nude mice grafted with human multiple myeloma cells are also used.
Other in-vivo assays which are used for testing the inhibitory effects of the backbone cyclized IL-6 antagonists are: IL-6 mediated acute-phase response, IL-6 mediated adjuvant 20 arthritis, and pancreatitis induced by taurocholic acid as described in the following examples.
The skilled artisan will appreciate that the following examples 25 are merely illustrative and s.exve a-s~ non limitative exemplification of the -principles of the present invention and that many variations and modifications are possible within the scope of the currently claimed invention as defined by the claims which follow.
EXAMPLES
Example 1. Detailed synthesis of PTR 5045
Trp-Arg-Lys-(D)Arg-Phe-AlaC3-Leu-Arg-(D)Tyr-AlaN3-NH2
Two grams of Tenta-Gel resin (0.22 mmol/g), were swelled in NMP in a reaction vessel equipped with a sintered glass bottom and placed on a shaker. All the Fmoc protecting groups were removed
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WO 00/72864 PCT/ILOO/00305
by reaction with 20% piperidine in NMP (2 times 10 minutes, 10 ml each) followed by NMP wash (5 times two minutes, 15 ml each). Fmoc removal was monitored by ultraviolet absorption measurement at 290 nm. The couplings of the amino acids: 5 Fmoc-Arg(pmc)-QH, Fmoc-Leu-OH, Fmoc-(D)Arg(pmc)-OH,
Fmoc-Lys(Boc)-OH, Fmoc-Arg(pmc)-OH, Fmoc-Trp(Boc)-OH were carried out with 4 eq (1.76 mmol) of the amino acid +PyBrop (4 equivalents, 1.76 mmol)+ DIEA (8 equivalents, 3.52 mmol) in NMP (10 ml) for 1.5 hour at room temperature. Reaction completion 10 was monitored by the qualitative ninhydrin test (Kaiser test). After each coupling, the peptide-resin was washed with NMP (5 times with 15 ml NMP, 2 minutes each). The coupling of Fmoc-(D)Tyr(t-Bu)-OH to AlaN3 building unit was carried out by use of 4eq of amino acid + a mixture of TPTU and ToPPyU(4 eq, 15 1.76 mmol) in 10 ml NMP + 8 eq DIEA, double coupling: first coupling 2h, second coupling overnight. The coupling of Fmoc-Phe-OH to AlaC3 building unit was carried out by the same manner. Coupling completion was monitored by HPLC . The Allyl/Aloc protecting groups were removed by reaction with 20 Pd(PPh3)4 and acetic acid 5%, morpholine 2.5% in CH2CI2, under argon, for 2 hours at room temperature. The peptide resin was washed with CHCI3( 3 times, 5 min 30 ML each) followed by NMP. Cyclization was carried out with PyBOP 3 equivalents, DIEA 6 equivalents, in NMP, at room temperature for 2h. Final Fmoc 25 deprotection was carried out with 20% piperidine in UMP as above. The peptide resin was washed with CH2CI2 and dried under reduced pressure. The peptide was cleaved from the resin by reaction with TFA 94%, water 2.5%, EDT 2.5%, TIS 1%, at 0°C for 15 minutes and 2 hours at room temperature under argon. The 30 mixture was filtered and the resin was washed with a small volume of TFA. The filtrate was placed in a rotary evaporator and all the volatile components were removed. An oily product was obtained. It was triturated with ether and the ether decanted, three times. A white powder was obtained. This crude 35 product was dried. The weight of the crude product was 400 mg. After purification by HPLC a single peak was obtained with 100% purity as detected by analytical HPLC and capillary
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electrophoresis. The expected mass of 1489.7 daltons was detected by mass spectroscopy.
Example 2: the.effect of backbone cyclic peptide analogs on B16.F10.9 melanoma cells growth.
Peptides were added to B16.F10.9 melanoma cells in the presence of 200 ng/ml IL-6 and 125 ng/ml sIL-6R. Incubation for three days. (Peptide concentration was calculated for average 10 molecular weight of 1500 Da. Sequence of control peptides: PTR 504 9: Trp-Arg-Lys-(D)Arg-Phe-AlaC3-Leu-Arg-Tyr-AlaN3-NH2 PTR 4041: Lys-GlyC2-Leu-Ile-Gln-Leu-Phe-GlyN3-Lys-Lys-NH2 The results described in figure 2 show that PTR 5045 and PTR 5041 fully block IL-6 activity at concentration of about 250 nM 15 while PTR 5049 and PTR 4041 are not active.
Example 3: The in-vivo effect of IL-6 antagonists on IL-6 mediated acute-phase response.
The objective was to establish a simple first-line in-vivo model, for testing the activity of IL-6 inhibitors. The turpentine model was chosen based on the principal role that IL-6 plays in this inflammatory response.
Systemic and localized inflammation elicit a general reaction in the organism, known as the acute phase response, which includes fever, loss of body weight, hypoglycemia, and changes in the serum levels of several plasma proteins produced by the liver. IL-6 is an important mediator of the acute-phase 30 reaction (see Heinrich et.al., Biochemistry J. 1 265:621, 1990 for a comprehensive review), together with IL-1 and TNF-a- It has been shown previously that sterile tissue damage caused by injection of turpentine induces an acute-phase reaction, and that IL-6 is an essential mediator of this response (Rokita 35 et.al., Cytokine 5:454, 1993).
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To confirm this role of IL-6 in this phenomenon we used IL-6-deficient mice generated by gene targeting (knock out). Method and Results
IL-6 knock-out (-/-) and matched wild-type (C57/Black; CB) mice were used. Sterile tissue damage was induced by subcutaneous injection of turpentine, 0.1 ml, into both hind limbs. IL-6 was determined in the serum by ELISA (QuantikineM, R&D). For liver acute-phase proteins, Fibrinogen was determined in citrated plasma, by the calcium method.
IL-6 levels rose 7-fold following turpentine injection in normal, but not in IL-6 deficient mice (Figure 3a).
Fibrinogen levels rose 3- to 4-fold following turpentine injection in normal, but not in IL-6 deficient mice (Figure 3b) .
Loss of body weight occurred following turpentine injection in normal, but not in IL-6 deficient mice (Figure 3c).
No changes in fibrinogen levels were detected 6 hours after turpentine injection. Elevated fibrinogen levels were observed at 12 hours post injection, and reach a maximal level by 24 hours post injection.
Conclusions
Our results confirm the previously published findings (Kozak et al., American J. Physiology 272:2 R621, 1997; Kopf. et-al., Nature 368:339-342, 1994), which suggest that IL-6 is an essential mediator of the acute-phase response to turpentine. The turpentine model can serve as a first-line in-vivo assay to determine the pharmacological efficacy of anti-IL-6 treatments.
PTR 5045 was tested in this model in compare to the non-relevant control peptide PTR 4041
(Lys-GlyC2-Leu-Ile-Gln-Leu-Phe-GlyN3-Lys-Lys-NH2) . The results are summarized in the following table 3:
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Table 3: The in-vivo effect of PTR 5045 on IL-6 mediated acute-phase response.
Mean weight loss
%
grams
PTR 4041 (control)
-7.3
-2.51
PTR 5045
-3.93
-1. 35
Student t-test
P=0.035
P=0.047
Mann-Whitney test
P=0.02 9
P=0.023
Ten mice received 1 or 10 mg/kg of each peptide analog.
PTR 5045 reduces by about half the effect mediated by IL-6 on body weight during acute inflammation. The difference between PTR 5045 and the control peptide is significant also if taking only the 1 mg/kg dose.
Example 4: IL-6 mediated adjuvant arthritis.
The objective was to establish an in-vivo model of rheumatoid arthritis (RA), for testing the activity of Interleukin-6 (IL-6) inhibitors. The adjuvant arthritis model was chosen 15 because it has clinical and pathological similarities to RA in humans, and based on the putative role that IL-6 plays in this inflammatory condition.
Rheumatoid arthritis is a chronic, multi-system autoimmune 20 disease, mainly characterized by a persistent inflammatory synovitis, usually involving peripheral joints in a symmetric distribution. IL-6 has been implicated in RA, since increased levels were found in serum and synovial fluid of RA patients, and these levels were correlated with clinical parameters of 25 inflammation (Miltenburg et al., British J. Rheumatology
:186, 1991). Adjuvant induced arthritis in rats is used as a model for human RA because adjuvant arthritic animals develop the inflammatory and immunologic features which are observed in RA patients. Furthermore, IL-6 levels are elevated in the serum 30 of arthritic rats, and the levels correlate with inflammation,
41
and with the progress of the syndrome.
Method and Results
Genetically susceptible Lewis rats were used. The arthritis is induced by a single injection of complete Freund's adjuvant (CFA), containing heat killed Mycobacterium Tuberculosis in oil (10 mg/ml). The animals were injected intradermally at the base of the tail. The arthritis developed two weeks after immunization, and involved the small joints of the extremities. The rats were then subjected to a clinical scoring of the inflamed joints, and to a histo-pathological evaluation. The rate of success in inducing arthritis is greater than 85%. Female rats are more susceptible than males.
Inflammation of the synovium, formation of pannus, erosion of cartilage and bone were all observed histopathologically, confirming the clinical severity.
Dexamethasone treatment completely abolished the clinical signs of arthritis, and can therefore be used as a positive control in this model. Delivery of the dexamethason treatment was successfully achieved by employing osmotic mini-pumps, which could also be used for the continuous administration of peptides.
Conclusions
Our results confirm the previously published descriptions of this RA model (Stanescu et al., Arthritis and Rheumatism 30:779, 1987).
The adjuvant arthritis model can serve as a disease model to determine the pharmacological activity of anti-IL-6 treatments. The testing is based on scoring of clinical parameters at the onset of the disease (day 12) .
Example 5: Pancreatitis Induced by Taurocholic Acid.
The objective is to establish an in-vivo model of acute pancreatitis for testing the activity of IL-6 inhibitors. The taurocholic acid induced pancreatitis model has clinical and
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pathological similarities to severe necrotizing acute pancreatitis.
In its severe form acute pancreatitis has clear systemic 5 manifestations such as: circulatory failure, metabolic acidosis, ascites, hyperglycemia, hyperlipidemia, and ultimately a multisystem organ failure. IL-6 has been implicated in acute pancreatitis, since elevated serum levels were more predictive of disease severity or lethality as 10 compared with C-reactive protein in patients with acute pancreatitis (Leser et al., Gastroenterology 101:782:5, 1991). Taurocholic acid induced pancreatitis in rats is used as a model for human pancreatitis because pancreatitis animals develop the biochemical and pathological features which are 15 observed in pancreatitis patients. Furthermore, IL-6 levels were elevated in the serum of pancreatitis rats.
Method and Results
Male Wistar rats were used. The pancreatitis was induced by the 20 infiltration of 0.5 ml of 10% sodium taurocholate, into several sites of the pancreatic parenchyma with a 30G needle. A progressive detergent effects took place, which resulted in a diffuse pancreatic necrosis, and a high mortality rate. The measured parameters were serum levels of the pancreatic-enzymes 25 amylase and lipase, serum IL-6, and mortality. In addition, a histopathological evaluation of the pancreas was performed. A mortality rate of 60-80% was found in the pancreatitis animals, with no mortality in the sham control group.
Severe hemorrhages and necrosis were evident in the pancreas, 30 after taurocholate induction.
Fat necrosis throughout the peritoneal cavity, and marked intestinal dilation were found at 24 hours.
A significant elevation in serum IL-6 was observed at three hours, and reached its peak within 6 hours from the 35 taurocholate injection.
A significant elevation of serum amylase was observed at two hours after pancreatitis induction.
43
Conclusions
Our results confirm the previously published findings, that IL-6 is elevated in animal models of pancreatitis. The taurocholate induced pancreatitis model can serve as a disease model to determine the pharmacological activity of anti-IL-6 treatments.
The testing is be based on measuring levels of pancreatic enzymes in the serum, mortality, and histopathological scoring.
Example 6: Synthesis and in vitro activity of further preferred backbone cyclized IL-6 antagonist PTRs.
Additional PTR analogs that were synthesized are listed in table 4, together with their respective chemical and biological data. Most of the peptides were synthesized during the initial phase of the research as part of the effort to discovery active peptides. The best IC50 were observed using the B16F10.9 cell assay are around 10 p./ml for PTR-5005 and around 20 j^g/ml for PTR-5037. Of these two peptides, only PTR-5005 appears to be active on TF1 cells.
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Table 4: Summary of synthesis and bioactivity of certain preferred PTRs.
PTR
TF1 inhibition (100 ug/ml)
Tl 165 inhibition (100 ug/ml)
B16F10.9 inhibition (33 ua/ml)
Sequence
5001
3
16
0
Thr-GlyC3-Gln-Gly-Ala-Ala-Ile-lle-GlyN3 -Gin-Pro
5003
32
36
T y r-Arg-Leu-Arg-Phe-G lyC 3 -Leu-Arg-Tyr -GlyN2
5005
98
132
37
Tyr-Arg-Leu-Arg-Phe-GlyC3-Leu-Arg-Tyr -GlyN2
5007
6
13
0
Tyr-Arg-Leu-Arg-Phe-GlyN2-Leu-Arg-Gly C3-Arg
5009
8
24
NT
GlyC3-Glu-Ser-Gln-Lys-GlyN3-Ala-Ala-Gln-Leu
5011
11
23
NT
Tyr-Arg-Leu-lle-Phe-Glu-GlyN2-Arg-Tyr-GlyC2
5013
28
22
NT
Tyr- Arg-Leu-Arg-Phe-G hi-GlyN2-Arg-Tyr -GlyC2
5015
21
19
NT
Tyr-Arg-Leu-Arg-Phe-Glu-GlyN2-Arg-Tyr -GlyC2
5017
NT •
NT
Arg-Leu-Arg-Ala-Glu-GJyC2-Ser-Lys-Gly N3-Phe
5019
14
NT
NT
Asp-Leu-Gln-GlyN3-Ser-Leu-Arg-Ala-Leu -Arg-Gln
5021
NT
NT
Asp-Leu-Gln-GlyN2-Ser-Leu-Arg-Ala-Leu -Arg-Gln
5023
11
NT
NT
Asp-Leu-Gln-GlyN2-Ser-Leu-Arg-Ala-Leu -Arg-Gln
5025
28
NT
NT
Asp-Leu-Gln-GlyN2-Ser-Leu-Arg-Ala-Leu -Arg-Gln
5027
56
NT
NT
T yr-Arg-Leu-Phe-Arg-GlyC3-Leu-Arg-T yr -GlyN2
5029
36
NT
NT
T yr-Arg-Leu-Arg-Phe-Glu-GlyN2-Arg-T yr -GlyC2
5031
NT
NT
Tyr-Arg-Lys-Arg-Phe-GlyN2-Leu-Arg-Gly C3-Arg
5033
NT
NT
Tyr-Arg-Lys-Arg-Phe-GlyN2-Leu-Arg-Gly C3-Arg
5035
2
NT
NT
Tyr-Arg-GlyN2-Arg-Phe-Gla-Leu-Arg-Gly C3-Arg
5037
1
NT
NT
Tyr-Arg-Leu-Arg-Phe-AlaC3-Leu-Arg-Tyr -AlaN3-Ala-Glu
5039
-14
NT
NT
Phe-Arg-Leu-Arg-Phe-AlaC3-Leu-Arg-Tyr -AlaN3
NT - Not Tested
Certain preferred analogs are described in table 5 and table 6.
45
PCT/ILOO/00305
Table 5: Certain preferred backbone cyclic peptide analogs capable of inhibiting IL-6 derived from either IL-6, IL-6R or gpl30.
No.
Origin
Sequence
01
IL-6R
Tyr
Arg
Leu
Arg
Phe
GlyN2
Leu
Arg
Tyr
GlyC 3
02
IL-6R
Tyr
Arg
Leu
Arg
Phe
GlyN2
Leu
Arg
GlyC3
Arg
03
IL-6R
Arg
Tyr
Arg
Ala
Glu
GlyC2
Ser
Lys
GlyN3
Phe
04
IL-6R
Ala
Glu
Arg.
Ser
Lys
Thr
Phe
Thr
Thr
Trp
05
IL-6R
GlyN3
Arg
GlyC3
Lys
Thr
Phe
Thr
Thr
Trp
Met
06
IL-6R
Ala
GlyC2
D/LArg
Phe
Lys
DThr
Phe
D/LThr
GlyN3
D/LTrp
07
IL-6R
Ala
Val
Ala
Arg
GlyC2
Pro
Arg
Trp
Leu
GlyN2
08
IL-6R
Ala
Val
Pro
Glu
GlyC2
Asp
Ser
GlyN2
Phe lie
08
IL-6R
Ala
Val
Pro
Glu
GlyC2
Asp
Ser
GlyN2
Tyr lie
09
IL-6R
Glu
Gly
GlyC2
Ser
Ser
Phe
Tyr
GlyN2
Val
Ser
IL-6R
Tyr
He
Val
Ser
GlyC2
Ala
Val
Ala
Ser
GlyN2
11
IL-6R
iGlyC2
Met
Ala
Val
Ala
Ser
Ser
Val
Gly
GlyN2
12
IL-6R
Ala
Val .
GlyC2
Ser
Ser
Val
Gly
GlyN2
Lys
Phe
13
IL-6R
Gly
Ala
GlyC2
lie
Leu
Gin
Pro
GlyN2
Pro
Pro
14
IL-6R
GlyC2
Gin
Pro
Asp
Pro
Pro
Ala
GlyN2
lie
Thr
IL-6R
Ser
Gin
GlyC2
Ser
Gin
Lys
Phe
Ser
Ala
GlyN2
16
IL-6
GlyC2
Asn
Leu
Pro
Lys
Met
Ala
Glu
Lys
GlyN2
17
IL-6
GlyC2
Lys
Val
Leu lie
Gin
Phe
GlyN2
Gin
Lys
18
gpl30
GlyC2
Asn
Phe
Thr
Leu
Lys
Ser
GlyN2
Trp
Ala
19
gpl30
Phe
Ala
Asp
Ala iGlyC2
Ala
Lys
Arg
Asp
GlyN2
gpl30
GlyC2
Thr
Pro
Thr
Ser
Ala
Thr
GlyN2
Asp
Tyr
21
gpl30
Asn
Phe
Asp
Pro
GlyC2
Tyr
Lys
Val
Lys
GlyN2
22
gpl30
Asn
Pro
GlyC2
His
Asn
Leu
Ser
Val lie
GlyN2
23
gpl30
Ser lie
GlyC2
Lys
Leu
Thr
Trp
Thr
Asn
GlyN2
24
gpl30
Tyr
Arg
GlyC2
Lys
Asp
Ala
Ser
GlyN2
Trp
Ser
gpl30
Arg
Thr
Lys
Asp
Ala
Ser
GlyC2
Trp
Ser
GlyN2
26
gpl30
GlyC2
lie
Pro
Pro
Glu
Asp
Thr
Ala
Ser .
GlyN2
27
gpl30
GlyC 2
Asp
Thr
Ala
Ser
Thr
Arg
Ser
Ser
GlyN2
28
gpl30
GlyC2
Ala
Ser
GlyN2
Arg
Ser
Ser
Phe
Thr
Val
29
gpl30
Ser
Phe
GlyC2
Val
Gin
Asp
Leu
Lys
Pro.
GlyN2 -
gpl30
Tyr
Val
Phe
Arg lie
Arg
GlyC2
Met
Lys
GlyN2
The average activity of the peptides found following the above procedure is estimated to be over 100 as estimated from the results of the MPS experiments.
46
WO 00/72864 PCT/ILOO/00305
Table 6: Summary of activity of certain preferred analogs derived from the IL-6R.
Sequence
TF1
B16F10.9
active at
Lys
Arg
Lys
(D)Arg
Phe
AlaC3
Leu
Arg
BTyr
AlaN3
85
<12 uM
Trp
Arg
Lys
(D)iArg
Phe
AlaC3
Leu
Arg
BTyr
AlaN3
32
<12 uM
Trp
Arg
Lys
(D) Arg
(D)Phe
AlaC3
Leu
Arg
BTyr
AlaN3
41
<12 uM
(D)Lys
Arg
(D)Leu
(D)Arg
(D)Phe
AlaC3
(D)Leu
Arg
(D) Tyr
AlaN3
92
47 uM
(D)Lys
Arg
Lys
Arg
(D)Phe
AlaC3
Lys
Arg
Tyr
AlaN3
55
62 uM
(D)Lys
Arg
Lys
(D)Arg
(D)Phe
AlaC3
Leu
Arg .
Tyr
AlaN3
13
62 uM
Tyr
Arg
Lys
(D)Arg
(D)Phe
AlaC3
Leu
(D)Arg
BTyr
AlaN3
19
47 uM
Lys
Arg
Lys
Arg
Phe
AlaC3
Lys
(D)Arg
BTyr
AlaN3
21
62 uM
(D) Lys
Arg
Lys
(D) Arg
Phe
AlaC3
(D)Leu
Arg
Tyr
AlaN3
3
62 uM
Lys
Arg
Leu
(D) Arg
(D)Phe
AlaC3
Lys
Arg
BTyr
AlaN3
22
not active
(D)Lys
Arg
Lys
Arg
Phe
AlaC3
Leu
Arg
(D)Tyr
AlaN3
not active
(D)Lys
Arg
Lys
Arg
(D)Phe
AlaC3
Leu
Arg
(D)Tyr
AlaN3
23
62 uM
(D)Lys
Arg
Lys
Arg
(D)Phe
AlaC3
Lys
(D)Arg
(D) Tyr
AlaN3
17
62 uM
(D)Lys
Arg
Lys
(D)Arg
(D)Phe
AlaC3
Lys
Arg
Tyr
AlaN3
17
62 uM
<D)Lys
Arg
Lys
Arg
Phe
AlaC3
Lys
Arg
(D)Tyr
AlaN3
21
not active
(D)Lys
Arg
Lys
Arg
Phe
AlaC3
Leu
(D) Arg
(D) Tyr
AlaN3
19
not active
(D)Lys
Arg
Lys
Arg
Phe
AlaC3
(D)Leu
(D)Arg
Tyr
AlaN3
27
not active
(D)Tyr
Arg
Lys
Arg
Phe
AlaC3
Lys
(D)Arg
(D) Tyr
AlaN3
22
not active
BTyr is a mixture of DTyr and LTyr, and thus these wells contain 2 peptides each.
The results in table 6 demonstrate a general agreement between the results of both types of bioassays. Most of the peptides tested which were positive on TF1 cells, were also positive on B16F10.9 cells.
The best peptide analogs obtained appear to inhibit the effect of IL-6 on B16F10.9 cells at theoretical crude concentrations below 12 uM, suggested IC50 values close to 1 uM. Somewhat higher IC50 values are observed in the TF1 assay.
47
Example 7: Design, synthesis, screening and identification of additional preferred backbone cyclized analogs derived from the IL-6 molecule.
Based on the crystal structure of IL-6 and experiments that correlate specific point mutations and IL-6 biological activity, crucial contact points in loop AB and helix D of the IL-6 molecule were determined (Xu et al. J. Mol. Biol., 268: 468, 1997, and Simpson et al. Protein Sci. 6:929, 1997 and references cited there).
Applying the methods for identifying pharmacophore containing molecules - from a virtual library (as disclosed in international patent application PCT IL/00/00218), a set of molecules that contained the pharmacophore and mimic the corresponding region of IL-6 protein were obtained. Those molecules were used for the design of combinatorial libraries of 107 different backbone cyclic molecules. The synthesis of one example of these libraries (ab0373) is described in the following scheme:
Step 1
Step 2
Step 3
Step 4
Step 5
AA-4 10
T
AA-7 10
AA-11 11
NBU-1 15b
1
AA-2 15
AA-5 17
AA-8 17
CBU-1 17
Step
CBU-3
AA-13
CBU-4
6
7
9
Wherein:
48
WO 00/72864 PCT/ILOO/00305
a NBU represents a building unit with amine reactive group b The number in the second line of each step represent the number of individual amino acids coupled in each split arm. c CBU represents a building unit with carboxyl reactive group.
The libraries were screened for binding of soluble IL-6. The information obtained was used for synthesis of backbone cyclic peptides in MPS format. Analyses for biological activity were performed on the TF1 human cell line.
Eighteen backbone cyclic peptides from the first MPS plate exhibit more then 45% inhibition at 1:10 dilution. Since the endpoint of the bioassay used is cell death, there is a need to check the specificity of the killing action, and to examine whether the cell death is due to inhibition of the IL-6 15 signaling pathway. The peptide analogs were therefore analyzed for their ability to induce non-specific cell death when the same cells were maintained with GM-CSF (instead of IL-6) as growth factor. The results of few of such activity and selectivity assays are summarized in Table 7 and Figure 4. 20 Some of the analogs exhibits non-specific inhibition (for example peptide 1,2 and 5 in table 7 and Figure 4) but some (i.e. peptide 34 and 41) were clearly specific to the IL-6 pathway.
49
Table 7. Activity and selectivity of selected backbone cyclized analogs as determined in TF1 cells bioassay.
Inhibition of IL-6 activity (%)
Experiment 23
Experiment 24
Peptide
WST
WST
JH-T
Number a
b
IL-6
GM-CSF
IL-6
GM-CSF
1
122
112
124
111
114
115
2
117
109
112
107
114
115
122
113
130
109
114
115
8
9
6
-36
29
-82
14
40
47
50
-41
65
-79
17
50
44
67
-23
80
-30
37
56
49
-59
78
-42
54
54
77
-49
104
26
27
-55
-186
-28
-64
-7
-86
33
116
119
112
39
113
70
34
97
108
96
-27
106
3
119
118
106
110
114
115
40
42
72
43
-45
61
-63
41
96
100
95
101
-13
45
-53
-144
-23
-39
18
-87
50
115
111
103
107
114
115
57
122
114
121
48
114
102
60
-1
2
11
-93
33
-151
61
54
58
86
4
58
-49
81
38
46
92
43
93
27
83
2
4
31
-5
51
12
88
96
98
112
103
114
115
91
98
106
123
45
113
75
92
-108
-152
-25
-79
8
-103
Anti IL-6R3
38
39
42
56
2
a Anti IL-6R antibody in concentration of 1.35 ug/ml used as positive control in the assays.
50
Claims (28)
1. A backbone cyclized peptide analog having IL-6 antagonist activity, comprising a peptide sequence of five to twenty amino acids that incorporates at least one building unit, said building unit containing one nitrogen atom of the peptide backbone connected to a bridging group comprising an amide, thioether, thioester or disulfide, wherein the at least one building unit is connected via the bridging group to form a cyclic structure with a moiety selected from the group consisting of a second building unit, the side chain of an amino acid residue of the sequence or the N-terminal amino acid residue.
2. The backbone cyclized analog of claim 1 wherein the peptide sequence comprises six to twelve amino acids.
3. The backbone cyclized analog of claim 1 wherein the peptide sequence incorporates at least one D-isomer of an amino acid.
4. The backbone cyclized analog of claim 1 wherein the peptide sequence incorporates at least two D-isomers of an amino acid.
5. The backbone cyclized analog of claim 1 wherein the linear peptide sequence is derived from the IL-6 receptor.
6. The backbone cyclized analog of claim 1 wherein the linear peptide sequence is derived from the IL-6 molecule.
7. The backbone cyclized analog of claim 1 having the general formula 1: R249 _R250 _R251 _R252 _R253 _NR254 _R255_ R256 _R257 -NR258 _X l(CH2)m-Y2- (CH2) 11' Formula No. 1 51 INTELLECTUAL PROPERTY OFFICE OF N.Z. 1 3 mar 2003 RECEIVED WO 00/72864 PCT/IL00/00305 wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R249 is Trp, (L) or (D)Lys, (L) or (D) Tyr or (D)Phe; R250 is Arg,; R251 is (L) or (D)Leu or Lys f r252 is (L) or (D)Arg; R253 is (D)- or (L)- Phe; R254 is Ala; R255 is (D)- or (L)- Leu or is Lys; R256 is absent or is (L) or (D) Arg; R257 is (L) or (D) Tyr; R258 is Ala; and Y2 is amide, thioether, thioester or disulfide.
8. The backbone cyclized analog of claim 7 wherein R249 is Trp, (L) - or (D)- Lys or (D)Phe; R250 is Arg; R251 is Lys or (D)Leu; R252 is (D) Arg; R253 is (D)- or (L) — Phe; R254 is Ala; R255 is (D)- or (L)- Leu; R256 is absent or is Arg; R257 is (D) Tyr; R258 is Ala; and Y2 is amide, thioether, thioester or disulfide.
9. The backbone cyclized IL-6 antagonist of claim 8 having the formula: Trp-Arg-Lys-(D)Arg-Phe-AlaC3-Leu-Arg-(D)Tyr-AlaN3-NH2
10. The backbone cyclized IL-6 antagonist of claim 8 having the formula: (D)Lys-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3-(D)Leu-Arg-(D)Tyr-AlaN3- NH2 52 10 15 WO 00/72864 PCT/IL00/00305
11. The backbone cyclized IL-6 antagonist of claim 8 having the formula: (D)Phe-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3-Leu-(D)Tyr-AlaN3-NH2
12. The backbone cyclized analog of claim 1 having the general formula 3: R1 ,NR2 R3 R4 NR5 R6-X L(CH2)m-Y:— (CH2)n "J Formula No. 3 wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R1 is (D)Bip, Gin, Lys, Lys(ZCL) or Dab; 20 R2 is (D)Lys, Gly, Ala or Trp R3 is Orn, 4PyrAla, (L) or (D)Dab, (D)Arg , Lys or Dpr; R4 is Lys, Lys(ZCL), Arg, Arg(Mtr) or (D)Glu; R5 is Asn, Trp or (D)Ala; R6 is Arg, (p-N02) Phe, (L)- or (D)- Trp, Gin, Abu or Glu; 25 and Y2 is amide, thioether, thioester or disulfide.
13. The backbone cyclized analog of claim 1 having the general formula 4: 30 NR1—R2 R3 —R4—NR5 NRS-X " ( CH2 ) m-Y2 ( CH2 ) n J 35 Formula No. 4 wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; 40 R1 is (D)Phe or Lys; R2 is (D)Cit, Lys or (D)Bip; . R3 is Dpr, 4PyrAla or (L)- or (D)- Arg; R4 is HomArg, Orn or Lys; 53 WO 00/72864 PCT/IL00/00305 R5 is (D)Gln or (L)- or (D)- Trp; R6 is (L)- or (D)- Gin or (p-N02)Phe; and Y2 is amide, thioether, thioester or disulfide. 5
14. A pharmaceutical composition comprising a backbone cyclized IL-6 antagonist comprising a peptide sequence of five to twenty amino acids that incorporates at least one building unit, said building unit containing one nitrogen atom of the peptide backbone connected to a bridging group 10 comprising an amide, thioether, thioester or disulfide, wherein the at least one building unit is connected via the bridging group to form a cyclic structure, together with a pharmaceutically acceptable carrier or diluent.
15 15. The pharmaceutical composition of claim 14 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the general formula 1: 20 25 r249_r250_r251_r252_r253_nr254_r255_r256_r257_nr258_x (CH2 ) m"Y2— ( CH2 ) n J Formula No. 1 wherein m and n are .1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R249 is Trp, (L). or (D)Lys, (L) or (D) Tyr or (D)Phe; r30 R250 is Arg; R251 is (L) or (D)Leu or Lys; R252 is (L) or (D)Arg; R253 is (D)- or (L)- Phe; R254 is Ala; 9 E, t 35 R is (D)- or (L)- Leu or is Lys; R256 is absent or is (L) or (D) Arg; R257 is (L) or (D) Tyr; R258 is Ala; and Y is amide, thioether, thioester or disulfide. 40 54 WO 00/72864 PCT/ILOO/00305
16. The pharmaceutical composition of claim 15 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the formula: Trp-Arg-Lys-(D)Arg-Phe-AlaC3-Leu-Arg-(D)Tyr-AlaN3-NH2
17. The pharmaceutical composition of claim 15 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the formula: (D)Lys-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3-(D)Leu-Arg-(D)Tyr-AlaN3- NH2
18. The pharmaceutical composition of claim 15 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the formula: (D)Phe-Arg-(D)Leu-(D)Arg-(D)Phe-AlaC3-Leu-(D)Tyr-AlaN3-NH2
19. The pharmaceutical composition of claim 14 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the general formula 3: R1 NR2 R3 R4 NR5 R6-X " (CH2) m-Y2 (CH2) n -J Formula No. 3 wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R1 is (D)Bip, Gin, Lys, Lys(ZCL) or Dab; R2 is (D)Lys, Gly, Ala or Trp R3 is Orn, 4PyrAla, (L) or (D)Dab, (D)Arg , Lys or Dpr; R4 is Lys, Lys(ZCL), Arg, Arg(Mtr) or (D)Glu; R5 is Asn, Trp or (D)Ala; R6 is Arg, (p-N02)Phe, (L)- or (D)- Trp, Gin, Abu or Glu; and Y2 is amide, thioether, thioester or disulfide.
20. The pharmaceutical composition of claim 14 wherein the IL-6 antagonist is a backbone cyclized peptide analog 55 NR1-- R2-- R3- R4-NR5—NR6- X having the general formula 4: J (CH2) m- Y2- (CH2) „■ Formula No. 4 wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R1 is (D) Phe or Lys; R2 is (D) Cit, Lys or (D) Bip; R3 is Dpr, 4PyrAla or (L) - or (D) - Arg; R4 is HomArg, Orn or Lys; R5 is (D) Gin or (L) - or (D) - Trp; R6 is (L) - or (D) - Gin or (P-NO2) Phe; and Y2 is amide, thioether, thioester or disulfide.
The use of a backbone cyclized IL-6 antagonist comprising a peptide sequence of five to twenty amino acids that incorporates at least one building unit, said building unit containing one nitrogen atom of the peptide backbone connected to a bridging group comprising an amide, thioether, thioester or disulfide, wherein the at least one building unit is connected via the bridging group to form a cyclic structure with a moiety selected from the group consisting of a second building unit, the side chain of an amino acid residue of the sequence or the N-terminal amino acid residue in the manufacture of a medicament for treating disorders selected from the group consisting of neoplasms, bacterial, parasite and viral infections, chronic autoimmune disorders and osteoporosis.
The use of a IL-6 antagonist as claimed in claim 21 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the general formula 1: R249. R250. R251. R252. R253. NR234- R25*5- R256- R257- NR258- X Formula No. 1 INTELLECTUAL PROPERTY OFFICE OF N.Z. 1 3 mar 2003 received 56 51549 3 25. wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R249 is Trp, (L) or (D) Lys, (L) or (D) Tyr or (D) Phe; R250 is Arg; R251 is (L) or (D) Leu or Lys; R252 is (L) or (D) Arg; R253 is (D) - or (L) - Phe; R254 is Ala; R255 is (D) - or (L) - Leu or is Lys; R256 is absent or is (L) or (D) Arg; R257 is (L) or (D) Tyr; R258 is Ala; and Y2is amide, thioether, thiester or disulfide.
The use of a IL-6 antagonist as claimed in claim 22 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the formula: Trp-Arg-Lys-(D) Arg-Phe-AlaC3-Leu-Arg-(D) Tyr-AlaN3-NH2.
The use of a IL-6 antagonist as claimed in claim 22 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the formula: (D) Lys-Arg- (D) Leu- (D) Arg- (D) Phe-AlaC3-(D) Leu-Arg- (D) Tyr-AlaN3-NH2.
The use of a IL-6 antagonist as claimed in claim 22 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the formula: (D) Phe-Arg- (D) Leu- (D) Arg- (D) Phe-AlaC3—(D) Leu-Arg- (D) Tyr (D) Tyr-AlaN3-NH2.
The use of a IL-6 antagonist as claimed in claim 21 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the general formula 3: Ri —- NR2 - R3 —- R4 -- NR5 — R« - X - J-(CH2) m-Y2-(CH2) ^ INTELLECTUAL PROPERTY OFFICE OF N.Z. Formula No. 3 1 3 mar 2003 RECEIVED 57 dJ, i ■ ./ L' ^ , wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R1 is (D) Bipl, Gin, Lys, Lys (ZCL) or Dab; R2 is (D) Lys, Gly, Ala or Trp R3 is Orn, 4PyrAla, (L) or (D) Dab, (D) Arg, Lys or Dpr; R4 is Lys, Lys (ZCL), Arg, Arg (Mtr) or (D) Glu; R5 is Asn, Trp or (D) Ala; R6 is Arg, (P-NO2) Phe, (L) — or (D) - Trp, Gin, Abu or Glu; and Y2 is amide, thioether, thioester or disulfide.
27. The use of a IL-6 antagonist as claimed in claim 21 wherein the IL-6 antagonist is a backbone cyclized peptide analog having the general formula 4: NR1- R2— R3- R4— NR5— NR6- X i-(CH2) m-Y2 - (CH2) n—' Formula No. 4 wherein m and n are 1 to 5; X designates a terminal carboxy acid, amide or alcohol group; R1 is (D) Phe or Lys; R2 is (D) Cit, Lys or (D) Bip; R3 is Dpr, 4PyrAla or (L) - or (D) - Arg; R4 is HomArg, Orn or Lys; R5 is (D) Gin or (L) — or (D) — Trp; R6 is (L) - or (D) - Gin or (P-NO2) Phe; and Y2 is amide, thioether, thioester or disulfide.
28. The use of a IL-6 antagonist as claimed in claim 21 wherein the disorder is selected from the group consisting of rheumatoid arthritis, multiple myeloma and osteoporosis. PIPERS Attorneys for PEPTOR LTD INTELLECTUAL PROPERTY OFFICE OF N.Z. 1 3 mar 2003 received 58
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL13023899A IL130238A0 (en) | 1999-06-01 | 1999-06-01 | Conformationally constrained backbone cyclized interleukin-6 antagonists |
PCT/IL2000/000305 WO2000072864A1 (en) | 1999-06-01 | 2000-05-28 | Conformationally constrained backbone cyclized interleukin-6 antagonists |
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NZ515493A true NZ515493A (en) | 2003-07-25 |
Family
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EP (1) | EP1187624A1 (en) |
JP (1) | JP2003500453A (en) |
AU (1) | AU770612B2 (en) |
CA (1) | CA2375657A1 (en) |
IL (1) | IL130238A0 (en) |
NZ (1) | NZ515493A (en) |
WO (1) | WO2000072864A1 (en) |
ZA (1) | ZA200109637B (en) |
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US6841533B1 (en) | 1995-12-07 | 2005-01-11 | Peptor Limited | Conformationally constrained backbone cyclized interleukin-6 antagonists |
GB2401040A (en) | 2003-04-28 | 2004-11-03 | Chugai Pharmaceutical Co Ltd | Method for treating interleukin-6 related diseases |
JP2005060303A (en) * | 2003-08-12 | 2005-03-10 | Sutaagen:Kk | Agent for treating or preventing osteoporosis caused by immobility |
PT2592081T (en) * | 2010-07-06 | 2017-05-03 | Ono Pharmaceutical Co | Tetrahydrocarboline derivative |
ES2778053T3 (en) | 2011-01-18 | 2020-08-07 | Bioniz Llc | Compositions to modulate gamma-c cytokine activity |
US9959384B2 (en) | 2013-12-10 | 2018-05-01 | Bioniz, Llc | Methods of developing selective peptide antagonists |
CN108350032A (en) | 2015-10-09 | 2018-07-31 | 比奥尼斯有限责任公司 | Adjust γ C- cytokine activities |
Family Cites Families (4)
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US5210075A (en) * | 1990-02-16 | 1993-05-11 | Tanabe Seiyaku Co., Ltd. | Interleukin 6 antagonist peptides |
JP3525221B2 (en) * | 1993-02-17 | 2004-05-10 | 味の素株式会社 | Immunosuppressants |
US5420109A (en) * | 1993-11-12 | 1995-05-30 | Houghten Pharmaceuticals, Inc. | Cytokine restraining agents |
WO1997048722A1 (en) * | 1996-06-20 | 1997-12-24 | The University Of Sheffield | Pyridine nucleotide-dependent enzymes |
-
1999
- 1999-06-01 IL IL13023899A patent/IL130238A0/en unknown
-
2000
- 2000-05-28 AU AU47763/00A patent/AU770612B2/en not_active Ceased
- 2000-05-28 EP EP00929763A patent/EP1187624A1/en not_active Withdrawn
- 2000-05-28 CA CA002375657A patent/CA2375657A1/en not_active Abandoned
- 2000-05-28 JP JP2000620973A patent/JP2003500453A/en active Pending
- 2000-05-28 WO PCT/IL2000/000305 patent/WO2000072864A1/en not_active Application Discontinuation
- 2000-05-28 NZ NZ515493A patent/NZ515493A/en unknown
-
2001
- 2001-11-22 ZA ZA200109637A patent/ZA200109637B/en unknown
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AU4776300A (en) | 2000-12-18 |
IL130238A0 (en) | 2000-06-01 |
WO2000072864A1 (en) | 2000-12-07 |
CA2375657A1 (en) | 2000-12-07 |
EP1187624A1 (en) | 2002-03-20 |
ZA200109637B (en) | 2002-11-22 |
JP2003500453A (en) | 2003-01-07 |
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