WO2002053184A2 - Utilisations de composes polycationiques - Google Patents

Utilisations de composes polycationiques Download PDF

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WO2002053184A2
WO2002053184A2 PCT/EP2002/000062 EP0200062W WO02053184A2 WO 2002053184 A2 WO2002053184 A2 WO 2002053184A2 EP 0200062 W EP0200062 W EP 0200062W WO 02053184 A2 WO02053184 A2 WO 02053184A2
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cpg
use according
antigen
poly
medicament
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PCT/EP2002/000062
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English (en)
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WO2002053184A3 (fr
Inventor
Karen Lingnau
Frank Mattner
Walter Schmidt
Max Birnstiel
Michael Buschle
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Intercell Ag
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Priority claimed from PCT/EP2001/000087 external-priority patent/WO2001054720A1/fr
Application filed by Intercell Ag filed Critical Intercell Ag
Priority to JP2002554133A priority Critical patent/JP2004519452A/ja
Priority to CA002433794A priority patent/CA2433794A1/fr
Priority to US10/250,953 priority patent/US7244438B2/en
Priority to EP02700194.0A priority patent/EP1347775B1/fr
Publication of WO2002053184A2 publication Critical patent/WO2002053184A2/fr
Publication of WO2002053184A3 publication Critical patent/WO2002053184A3/fr
Priority to US11/757,007 priority patent/US20080025996A1/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
    • A61K47/645—Polycationic or polyanionic oligopeptides, polypeptides or polyamino acids, e.g. polylysine, polyarginine, polyglutamic acid or peptide TAT
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55516—Proteins; Peptides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55561—CpG containing adjuvants; Oligonucleotide containing adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55572—Lipopolysaccharides; Lipid A; Monophosphoryl lipid A
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the invention relates to new uses for polycationic compounds .
  • polycationic compounds for example the polycationic amino acid polymers poly- -arginine and poly-L-ly- sine, have been shown to allow very efficient charging of antigen presenting cells (APCs) with antigens in vitro and in vivo. This is thought to be the key event for triggering immune cascades, eventually leading to the induction of antigen specific immune effector cells that are able to destroy or neutralise targets. It has been shown previously that a number of polycationic compounds excert effects on immune cells (Buschle et al . , Gene Ther.Mol.Biol. 1 (1998), 309-321; Buschle et al . , Proc.Natl.Acad.Sci. USA, 94 (1997), 3256-3261).
  • Co-injection of a mixture of poly-L-arginine and poly-L-lysine together with an appropriate antigen as a vaccine protects animals from tumor growth in several animal models .
  • a vaccine consisting of polycationic compounds and antigens is accepted in the art as being a very effective form of treatment (WO 97/30721) .
  • polycationic compounds for the preparation of a medicament with retarded in vivo release. It has surprisingly been found out in the course of the present invention that polycationic compounds, if applied to ⁇ gether with other pharmaceutically active compounds, which are quickly distributed in the individual, when administered without polycationic compounds, exhibit an effect of a retarded re ⁇ lease of the active compound from the site of administration.
  • the polycationic compound seems to keep the active pharmaceutical compound in a depot which allows a retarded in vivo release of the medicament which is often desired for an effective treatment with the pharmaceutically active principle.
  • an important field, where such a retarded in vivo release is advantageous is vaccination. If an antigen is presented for an extended period of time to the immune system of an individual to be vaccinated, the immune system has an enhanced possibility to create an efficient immune response against such an antigen. If, on the other hand, such an antigen is quickly distributed throughout the body, the antigen is quickly degraded and diluted so that an efficient immune response may not be achieved for many promising antigens .
  • polycationic compounds therefore are used for providing a depot of e.g. such an antigen, which allows a long lasting continuous and effective presentation of this antigen to the immune system in order to create a protective immunity.
  • the antigens are applied in combination with immunostimulatory compounds (e.g. CpG-ODN) , the slow release of these immunostimulatory compounds from the depot should result in a continuous stimulation of the immune system.
  • immunostimulatory compounds e.g. CpG-ODN
  • the present invention is especially beneficial if the combined medicament is administered, e.g. subcutaneously, intravenously, intranasally, intramusculary, intradermally or transdermally.
  • other application forms such as parenteral or topical application, are also suitable for the present invention.
  • the depot effect seems to be mostly significant if the composition is injected or implanted.
  • the present invention is preferably used in connection with all medicaments for which a retarded in vivo release is desired, e.g. antigens, allergens, drugs, which include cytokines, chemokines, immunostimulatory nucleic acids, cytotoxic drugs or anti-angio- genie drugs or compounds needed for wound healing.
  • medicaments for which a retarded in vivo release e.g. antigens, allergens, drugs, which include cytokines, chemokines, immunostimulatory nucleic acids, cytotoxic drugs or anti-angio- genie drugs or compounds needed for wound healing.
  • the antigen to be used within the course of the present invention is not critical, it may preferably be selected from the group consisting of an antigen from a viral, bacterial or a parasitic pathogen, an antigen from an eucaryotic pathogen, a tumor antigen, an autoimmune antigen or mixtures thereof. Especially preferred are negatively charged antigens or hydrophobic antigens . Further examples of antigens are whole-killed organisms, such as inactivated viruses or bacteria, fungi, protozoa or even cancer cells. Antigens may also consist of subfractions of these organisms/tissues, of proteins, or, in their most simple form, of pep- tides .
  • Antigens can also be recognised by the immune system in form of glycosylated proteins or peptides and may also be or contain polysaccharides or lipids.
  • Short peptides can be used, since e.g. cytotoxic T cells (CTL) recognise antigens in form of short usually 8-11 amino acids long peptides in conjunction with major histocompatibility complex (MHC) .
  • CTL cytotoxic T cells
  • MHC major histocompatibility complex
  • B cells recognise longer peptides starting at around 15 amino acids. By contrast to T cell epitopes, the three dimensional structure of B cell antigens may also be important for recognition by antibodies .
  • Preferred pathogens are selected from human immune deficiency virus (HIV) , hepatitis A and B viruses, hepatitis C virus (HCV) , Rous sarcoma virus (RSV) , Epstein Barr virus (EBV) , Influenza virus, Rotavirus, Staphylococcus aureus, Chlamydia pneumoniae, Chlamydia trachomatis, Mycobacterium tuberculosis, Streptococcus pneumoniae, Bacillus anthracis, Vibrio cholerae, Plasmodium sp. (PI. falciparum, Pi. vivax, etc.), Aspergillus sp. or Candida al- bicans .
  • HCV human immune deficiency virus
  • HCV hepatitis A and B viruses
  • HCV hepatitis C virus
  • RSV Rous sarcoma virus
  • EBV Epstein Barr virus
  • Influenza virus Influenza virus
  • Antigens may also be molecules expressed by cancer cells (tumor antigens) . Antigens may also be derived antigens. The derivation process may include the purification of a specific protein from the pathogen/cancer cells, the inactivation of the pathogen as well as the proteolytic or chemical derivatisation or stabilisation of such a protein. In the same way also tumor antigens (cancer vaccines) or autoimmune antigens may be used together with a polycationic compound according to the present invention.
  • the polycationic compound(s) to be used according to the present invention may be any polycationic compound, which shows e.g. the characteristic effect according to the WO 97/30721, or others like cationic liposomes, poly-ethylene-amine, chitosan or poly- cations for DNA transfer.
  • Preferred polycationic compounds are selected from basic polypeptides, organic polycations, basic polyaminoacids or mixtures thereof. These polyaminoacids should have a. chain length of at least 4 amino acid residues (see: Tuft- sin as described in Goldman et al (1983)) .
  • substances containing peptidic bounds like polylysine, polyarginine and polypeptides containing more than 20%, especially more than 50% of basic amino acid residues in a range of more than 8, especially more than 20, amino acid residues or mixtures thereof.
  • Other preferred polycations and their pharmaceutical compositons are described in WO 97/30721 (e.g. polyethyleneimine) and WO 99/38528.
  • these polypeptides contain between 5 and 500 amino acid residues, especially between 10 and 200 residues.
  • polycationic compounds may be produced chemically or recom- binantly or may be derived from natural sources .
  • Cationic (poly) peptides may also be polycationic anti-bacterial microbial peptides with properties as reviewed in (Ganz and Le- hrer, 1999; Hancock, 1999). These (poly)peptides may be of pro- karyotic or animal or plant origin or may be produced chemically or recombinantly (Andreu and Rivas , 1998; Ganz and Lehrer, 1999; Simmaco et al . , 1998). Peptides may also belong to the class of defensins (Ganz, 1999; Ganz and Lehrer, 1999) .
  • Such host defense peptides or defensines are also a preferred form of the polycationic polymer according to the present invention.
  • a compound allowing for activation (or down- regulation) of the adaptive immune system, preferably mediated by APCs (including dendritic cells) is used as polycationic polymer.
  • cathelicidin derived anti-microbial pep- tides or derivatives thereof (A 1416/2000, incorporated herein by reference) , especially anti-microbial peptides derived from mam ⁇ mal cathelicidin, preferably from human, bovine or mouse.
  • Polycationic compounds derived from natural sources include HIV- REV or HIV-TAT (derived cationic peptides, antennapedia peptides, chitosan or other derivatives of chitin) or other peptides derived from these peptides or proteins by biochemical or recombi- nant production.
  • Other preferred polycationic compounds are cathelin or related or derived substances from cathelin.
  • mouse cathelin is a peptide which has the amino acid sequence NH 2-RLAGLLRKGGEKIGEKLKKIGOKIKNFFQKLVPQPE-COOH.
  • Related or derived cathelin substances contain the whole or parts of the cathelin sequence with at least 15-20 amino acid residues.
  • Derivations may include the substitution or modification of the natural amino acids by amino acids which are not among the 20 standard amino acids. Moreover, further cationic residues may be introduced into such cathelin molecules . These cathelin molecules are preferred to be combined with the antigen and the immunogenic ODNs according to the present invention. However, these cathelin molecules surprisingly have turned out to be also effective as an adjuvant for an antigen without the addition of further adjuvants. It is therefore possible to use such cathelin molecules as efficient adjuvants in vaccine formulations with or without further immunostimulating substances.
  • Another preferred polycationic substance to be used according to the present invention is a synthetic peptide containing at least 2 KLK-motifs separated by a linker of 3 to 7 hydrophobic amino acids (A 1789/2000, incorporated herein by reference).
  • polycationic compounds may according to the present invention be preferably used together with a drug for which side effects due to a quick spread throughout the body of an individual are known.
  • the polycationic compound and the drug supposed to be released slowly are administered together at the same time and at the same site.
  • such drugs may be e.g. simply mixed with the polycationic compounds or provided as a covalently combined medicament.
  • Preferred compounds with inflammatory potential to be used within the course of the present invention are immunogenic nucleic acid molecules. It is known that the immune system of mammals (and probably most if not all vertebrates) recognises DNA of lower organisms, including bacteria probably due to structural and sequence usage differences between pathogen and host DNA.
  • oligodeoxynucleotides containing non-methylated cytosine-guanine dinucleotides (CpG) in a certain base context
  • ODNs oligodeoxynucleotides
  • CpG motifs are found at the expected frequency in bacterial DNA but are much less frequent in vertebrate DNA.
  • non-vertebrate (i.e. bacterial) CpG motifs are not methylated, whereas vertebrate CpG sequences are.
  • ODNs containing CpG motifs can directly activate monocytes and B cells.
  • CpG-ODNs the activation of mono- cytes and NK cells by CpG-ODNs promotes the induction of a Thl- type response and the development of cytotoxic T cells .
  • immunogenic ODNs are used as vaccine adjuvants to enhance the antibody response to specific antigens (e.g. EP 0 468 520 A2 , WO 96/02555, WO 98/16247, etc.).
  • CpG-ODNs When CpG-ODNs are applied in combination with an antigen to an animal, the CpG-ODN molecules are quickly distributed throughout the body without providing an effective minimum concentration at the site of administration where the desired effect should be initiated. It could be shown by the present animal model that the polycationic compounds inhibit the immediate spread of these molecules and induce the formation of a depot of CpG-ODNs at the injection site which resulted in a strongly prolonged CpG-ODN induced antigen specific immune response in vivo. This CpG-ODN model therefore was excellent for showing the depot effect of polycationic compounds.
  • CpG-ODNs are applied in combination with an antigen via injection, the CpG-ODN molecules are quickly distributed throughout the body without providing an effective minimum concentration at the site of administration where the desired effect should be initiated. It could be shown by the present animal model that the polycationic compounds inhibit the immediate spread of these molecules and induce the formation of a depot antigen and CpG-ODNs at the injection site, which resulted in a strongly prolonged CpG-ODN induced antigen-specific immune response in vivo.
  • a preferred embodiment of the present invention is characterised in that the medicament is to be applied together with the polycationic compound further comprises immunogenic oli- godesoxy nucleic acid molecules (ODNs), especially ODNs containing CpG motifs (CpG-ODNs) , inosine containing ODNs (I-ODNs) or mixtures or combinations thereof.
  • ODNs immunogenic oli- godesoxy nucleic acid molecules
  • CpG-ODNs ODNs containing CpG motifs
  • I-ODNs inosine containing ODNs
  • the induction of a depot effect according to the present invention is of course most desired for pharmaceutically active substances which are supposed to act locally at the given administration site. Therefore, the invention is significantly advantageous for substances, which should act locally but are easily transported and diffused away from this site by diffusion of transportation processes in the body.
  • substances may include antigens, allergens, cytokines, chemokines , immunostimulatory nucleic acids, cytotoxic drugs or anti-angiogenic drugs or compound needed for wound healing.
  • a preferred embodiment of the present invention relates to the use of the polycationic substances in combination with substances which otherwise rapidly diffuse from the administration site, i.e. have a rather short pharmacological half life, especially with respect to the site of administration. Therefore, preferred rapidly diffusing substances with a pharmacological half life (drop of the concentration of the substance by half) , especially at the site of administration, of below 10 minutes, more preferred below 5 minutes, especially below 1 minute.
  • such substances to be applied together with polycationic compounds in order to achieve a depot effect show a certain affinity to the polycationic compound, i.e. hydrophobic interaction, hydrogen bridges, electrostatic interactions, polar or ionic interactions.
  • the depot effect may also be achieved by covalent binding of the components in the combined pharmaceutical preparation; although non-covalent interactions of drug and polycationic compounds are preferred.
  • this strong local immune response (day 4/draining lymph node cells) induced after one single injection of an antigen with a mixture of polycationic compounds (as an example polyarginine pR 60 is used) and CpG-ODNs converts to a systemic immune response which is very long lasting.
  • the complex formation ability of substances such as CpG-ODNs with polycationic compounds is used for preventing a systemic distribution and the subsequent fast resorption of such substances, thereby providing a strong prolongation of the properties of such substances, e.g. a prolongation of the immunostimulatory properties of CpG-ODNs.
  • preventing the systemic distribution avoids the induction of potential harmful systemic side effects of immunostmulatory agents.
  • Ovalbumin-derived peptide OVA257-264
  • model compound a model antigen
  • the present invention also relates to treating a patient with a drug, supposed to be retardedly released in vivo comprising administering that drug together with an effective amount of a polycationic compound inducing a depot effect of that drug.
  • polycationic compound to be administered is highly depending on the necessities of the individual composition and optionally on the drug to be administered together with the polycationic polymer.
  • preferred amounts of polycation are 0.001-1000 ⁇ g/administration unit, more preferred 0,1-10 g/dose, especially around or beyond 0,1 mg/20g body weight (of mice) or the equivalent dose for hu ⁇ mans .
  • Fig. 1 shows that the combined application of poly-L-arginine, CpG-ODN and antigen induces strong antigen-specific immune responses which are systemic and very long lasting.
  • the figure shows peripheral blood lymphocytes stimulated ex vivo with OVA 257-
  • Fig. 2a shows that poly-L-arginine induces the formation of a depot at the injection site.
  • This figure shows photos from the injection sites at the indicated time points after vaccination.
  • White lines surround the area where the fluorescence labelled compounds of the vaccine can be detected;
  • Fig. 2b shows that the co-application of poly-L-arginine inhibits the spreading of CpG-ODN-Cy5 throughout the body.
  • This figure shows FACS analyses of lymphoid and non-lymphoid tissues at -day 1 after injection of CpG-0DN-Cy5 (B) or CpG-ODN-Cy5 and pR 60-FITC (C) . Untreated mice were used as a control (A) ;
  • Fig. 3 shows that poly-L-arginine induces the formation of a depot at the injection site when co-injected at least with one more molecule. This figure shows photos from the injection sites at day 4 after vaccination;
  • Fig. 4 shows that co-injected poly-L-arginine prevents the CpG- ODN-induced systemic production of TNF- ⁇ and IL-6 in vivo.
  • Mice were injected into the hind footpads and one hour later serum was prepared. The amount of TNF- ⁇ and IL-6 in the sera was determined by ELISA; E X A M P L E S
  • T R P-2 181-188-p ⁇ eptide-FITC yellow
  • poly-L-arginine-TRITC red-vio- let
  • CpG-0DN-Cy5 blue
  • 188-peptide-FITC was injected either alone or in combination with
  • CpG-0DN-Cy5 the peptide was not detectable at the injection site at day 4.
  • the injection of poly-L-arginine-TRITC alone resulted in its distribution all over the skin.
  • the injection of CpG-ODN- Cy5 either alone or in combination with TRP-2, __ . _ -peptide-FITC resulted in the distribution of CpG-0DN-Cy5 all over the skin.
  • This experiment also indicates that. poly-L-arginine only induced the- formation of a depot when it was injected with at least one more molecule (peptide and/or CpG-ODN) .
  • CpG-ODNs are described to have potentially harmful side effects in that they induce the systemic release of high amounts of pro-inflammatory cytokines such as TNF- ⁇ and IL-6, which could induce a shock syndrome (Sparwasser 1997, Lipford 1997) .
  • cytokines such as TNF- ⁇ and IL-6
  • Sparwasser 1997, Lipford 1997) cytokines
  • CpG-ODNs are not systemically present when injected in combination with poly-L-arginine. Therefore, it was investigated whether the co-administration of poly-L-arginine affects the CpG-ODN-induced systemic production of TNF- ⁇ and IL-6. Serum levels of both cytokines were determined by ELISA one hour after injection.
  • Example 4 demonstrates that neither the injection of OVA 2s7 _ 2g4 -peptide alone nor in combination with poly-L-arginine led to the induction of significant amounts of TNF- ⁇ and IL-6 in the serum, whereas the injection of OVA 25.,7-2 __64-peptide in combination with CpG-ODN induces high concentrations of both cytokines.
  • OVA 257 _ 264 -peptide with poly-L-ar- ginine and CpG-ODN, this systemic production of TNF- ⁇ and IL-6 was totally abolished.
  • CDllc + dendritic cells were incubated either with poly-L-arginine, CpG-ODN or the combination of poly-L- arginine and CpG-ODN (example 5) .
  • the levels of TNF- ⁇ and IL-6 were determined in the supernatants derived from these cultures .
  • poly-L-arginine also inhibits the polyinosinic-polycytidylic acid-induced production of pro-inflammatory cytokines by human dendritic cells .
  • mice were injected into each hind footpad with a total volume of lOO ⁇ l (50 ⁇ l per footpad) containing the above mentioned compounds.
  • Blood was taken via the tail vein at the indicated time points and peripheral blood lymphocytes (PBLs) were isolated using a Ficoll gradient. PBLs were stimulated ex vivo with the antigen used for vaccination/ with medium (background) and Conca- navalin A (positive control) .
  • IFN- ⁇ -ELISPOTs were carried out as described (Miyahira et al., 1995). This method is a widely used procedure allowing the quantification of antigen-specific T cells. Spots representing single IFN- ⁇ producing T cells were counted and the number of background spots was substracted from all samples. There were many spots detected after the stimulation with Con A (data not shown) indicating a good condition of the used lymphocytes. For each experimental group of mice the number of spots/lxlO 6 PBLs are illustrated in Figure 1.
  • Poly-L-arginine induces the formation of a depot at the injection site
  • FITC fluorescein
  • mice On day 0 mice were injected subcutaneously into the right flank with a total volume of lOO ⁇ l containing the above mentioned compounds . Animals were sacrificed at the indicated time points after injection and photos were taken from the injection sites (Fig. 2a) .
  • FITC fluorescein
  • mice were injected subcutaneously ' into the right flank with a total volume of lOO ⁇ l containing the above mentioned compounds.
  • mice were sacrificed and FACS-analyses were performed from secondary lymphoid organs (draining lymph node, spleen) as well as non-lymphoid tissues (lung, liver, kidney, heart) (Fig. 2b) .
  • Poly-L-arginine induces the formation of a depot at the injection site when co-injected at least with one more molecule
  • TRP-2-Peptide VYDFFVWL
  • H-2Kb MHC class I
  • HPLC HPLC purified and analysed by mass spectroscopy for purity.
  • fluorescein (FITC) labeling the TRP-2 1 o 8 ⁇ 1—18 o 8-peptide was dissolved in
  • the poly-L-arginine was dissolved in 50mM HEPES pH 7,9 (10mg/500 ⁇ l) .
  • the solution was kept at room temperature in the dark for 2,5 hours. Unreacted dye was separated by running the mixture over a PD10 column (Pharmacia, Uppsala, Sweden), using 50mM Hepes, pH 7 , 9 , as eluent.
  • TRP-2 isi _ i88 -FITC + CpG-ODN-Cy5 7 .
  • mice were injected subcutaneously into the right flank with a total volume of lOO ⁇ l containing the above mentioned compounds. Animals were sacrificed at day 4 after injection and photos were taken from the injection sites (Fig. 3).
  • CpG-ODN 1668 phosphothioate-modified oligodeoxynucleotides containing a CpG motif TCC ATG ACG TTC CTG ATG CT, synthesised by NAPS GmbH, G ⁇ ttingen. Dose: 5 nmol/mouse
  • mice 4 mice per .group
  • mice were injected into each hind footpad with a total volume of lOO ⁇ l (50 ⁇ l per footpad) , containing the above mentioned compounds .
  • the amount of the pro-inflammatory cytokines TNF- ⁇ and IL-6 in the sera was determined by cytokine- specific ELISAs according to the manufacturer's instructions (R&D Systems, Inc., Minneapolis, MN) .

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Abstract

La présente invention concerne l'utilisation d'un composé polycationique pour la préparation d'un médicament à libération in vivo retardée.
PCT/EP2002/000062 2001-01-05 2002-01-07 Utilisations de composes polycationiques WO2002053184A2 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP2002554133A JP2004519452A (ja) 2001-01-05 2002-01-07 ポリカチオン性化合物の用途
CA002433794A CA2433794A1 (fr) 2001-01-05 2002-01-07 Utilisations de composes polycationiques
US10/250,953 US7244438B2 (en) 2001-01-05 2002-01-07 Uses for polycationic compounds
EP02700194.0A EP1347775B1 (fr) 2001-01-05 2002-01-07 Utilisation de substances polycationiques en tant qu'adjuvants pour vaccins
US11/757,007 US20080025996A1 (en) 2001-01-05 2007-06-01 Methods and Compositions Comprising Polycationic Compounds

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EPPCT/EP01/00087 2001-01-05
PCT/EP2001/000087 WO2001054720A1 (fr) 2000-01-28 2001-01-05 Composition pharmaceutique pour immunomodulation et preparation de vaccins comprenant un antigene, un oligodesoxyribonucleotide immunogene et polymere polycationique sous forme d'adjuvants
ATA672/2001 2001-04-25
AT6722001 2001-04-25

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EP1347775A2 (fr) 2001-01-05 2003-10-01 Intercell AG Utilisation de substances polycationiques en tant qu'adjuvants pour vaccins
JP2006521320A (ja) * 2003-03-24 2006-09-21 インターツェル・アクチェンゲゼルシャフト 改良型ワクチン
WO2011101465A1 (fr) 2010-02-19 2011-08-25 Intercell Ag Nanoparticules d'ic31
KR101586200B1 (ko) * 2014-12-31 2016-01-18 성균관대학교산학협력단 면역자극 조성물, 이의 제조 방법, 및 이를 포함하는 면역요법 조성물

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WO2002032451A1 (fr) * 2000-10-18 2002-04-25 Intercell Biomedizinische Forschungs- Und Entwicklungs Ag Composition de vaccin

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1347775A2 (fr) 2001-01-05 2003-10-01 Intercell AG Utilisation de substances polycationiques en tant qu'adjuvants pour vaccins
JP2006521320A (ja) * 2003-03-24 2006-09-21 インターツェル・アクチェンゲゼルシャフト 改良型ワクチン
JP2011042678A (ja) * 2003-03-24 2011-03-03 Intercell Ag 改良型ワクチン
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WO2011101465A1 (fr) 2010-02-19 2011-08-25 Intercell Ag Nanoparticules d'ic31
US8765148B2 (en) 2010-02-19 2014-07-01 Valneva Austria Gmbh 1C31 nanoparticles
US9248180B2 (en) 2010-02-19 2016-02-02 Valneva Austria Gmbh IC31 nanoparticles
KR101586200B1 (ko) * 2014-12-31 2016-01-18 성균관대학교산학협력단 면역자극 조성물, 이의 제조 방법, 및 이를 포함하는 면역요법 조성물

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EP1347775B1 (fr) 2016-11-30
CA2433794A1 (fr) 2002-07-11
JP2004519452A (ja) 2004-07-02
EP1347775A2 (fr) 2003-10-01
WO2002053184A3 (fr) 2002-09-19

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