Patent application title: EXPANDING THE T CELL REPERTOIRE TO INCLUDE SUBDOMINANT EPITOPES BY VACCINATION WITH ANTIGENS DELIVERED AS PROTEIN FRAGMENTS OR PEPTIDE COCKTAILS
Claus Aagaard (Kobenhavn S, DK)
Jes Dietrich (Kobenhavn Nv, DK)
Peter Andersen (Bronshoj, DK)
Peter Andersen (Bronshoj, DK)
STATENS SERUM INSTITUT
IPC8 Class: AA61K3929FI
Class name: Drug, bio-affecting and body treating compositions preparations characterized by special physical form liposomes
Publication date: 2012-06-21
Patent application number: 20120156282
A convenient way of inducing a broad recognition of dominant and
subdominant responses to epitopes of any given antigen of importance for
prophylaxis or treatment of a chronic disease is provided. The method
involves immunizing with pools of overlapping fragments (synthetic
peptides, e.g., 10-30 mers with 2-20 aa overlap) of the desired antigen
in appropriate adjuvants. The T cell repertoire is primed to include not
only the immunodominant epitope recognized when the intact molecule is
used for immunization and induced by the chronic infection itself, but
induce a much broader and balanced response to a number of the
subdominant epitopes as well. The vaccination with peptide mix induces a
T-cell response that includes response to subdominant epitopes is
important for protection against chronic disease that on their own
induces a response focused only on immunodominant epitopes.
1. An immunogenic composition against a chronic disease such as a
bacterial, viral or parasitic infection or cancer comprising a peptide
mixture consisting of adjacent overlapping peptides spanning the whole
amino acid sequence of a protein that is expressed during the chronic
phase of the disease, wherein the peptides are from a hepatitis C virus
3. The immunogenic composition according to claim 1, where the peptides are independently 10 to 30 amino acids long.
4. The immunogenic composition according to claim 3, wherein the peptides are independently 12 to 20 amino acids long.
8. The immunogenic composition according to claim 1, delivered in a delivery system comprising an adjuvant.
9. The immunogenic composition according to claim 8, where the adjuvant is based on cationic liposomes.
10. The immunogenic composition according to claim 8, where the peptides are delivered encapsulated in the liposomes.
11. The immunogenic composition according to claim 9, where one or more of the peptides are lipidated.
12. The immunogenic composition according to claim 9, where each peptide in the peptide mix is mixed or incorporated individually into liposomes prior to making the peptide mixture.
13. The immunogenic composition according to claim 8, where the adjuvant is DDA/TDB.
14. A method of preparing an immunogenic composition according to claim 1, where the peptide mixture is prepared by proteolytic cleavage of the protein with two or more proteolytic cleavage agents.
15. The method of preparing an immunogenic composition according to claim 14, where the proteolytic cleavage agent is chosen among proteolytic enzymes such a trypsin, V-8 protease, AspN or chymotrypsin or chosen among chemical agents such as CNBr or BNPS-skatole.
16. A method for prophylaxis or treatment of a chronic disease in an animal comprising administering to the animal the immunogenic composition according to claim 1.
17. The method according to claim 16 where the prophylaxis or treatment is boosted by administering a second immunogenic composition comprising the full size protein spanned by the peptide mixture in adjuvant or expressed in a live delivery system.
21. The method according to claim 16, wherein said animal is a mammal.
22. The method according to claim 21, wherein said mammal is a human.
CROSS-REFERENCE TO RELATED APPLICATIONS
 This application is a continuation of U.S. patent application Ser. No. 11/823,402, filed Jun. 27, 2007, which claims the benefit under 35 USC 119(e) of prior U.S. Provisional Patent Application No. 60/817,947, filed Jun. 30, 2006, which applications are incorporated by reference herein.
BACKGROUND OF THE INVENTION
 The present invention provides a vaccine against chronic diseases such as a bacterial, viral or parasitic infection or cancer, a method of making such vaccines and prophylaxis and treatment of chronic disease.
 Compared to the limited number of diseases where vaccines are currently available, a very large number have so far escaped attempts to develop efficient vaccines. A common characteristic for many of these infectious diseases as well as cancer is that they develop slowly and manifest themselves as chronic diseases where the disease is maintained for years in the face of an existing host immune response. This often eventually results in immunopathology that is some cases, such as Chlamydia trachomatis, is the real cause of the human disease such as inflammatory scarring of the oviduct resulting in infertility. For some diseases such as Mycobacterium (M.) tuberculosis infection (TB), a vaccine exists. However, while the vaccine may prevent the acute manifestations of the disease, the bacteria is not cleared and a chronic or latent disease is established. TB runs essentially through 3 phases. During the acute phase, the bacteria proliferate in the organs, until the immune response increases to the point at which it can control the infection, whereupon the bacterial load peaks and starts declining. After this, a chronic or latent phase is established where the bacterial load is kept stable at a low level. In this phase M. tuberculosis goes from active multiplication to a state of slow or non-replicating persistence. In some cases such as TB, the infection can suddenly reactivate and overt disease will result. The factors that lead to this reactivation are largely unknown. In other cases such as Chlamydia, the infection may remain asymptomatic but the ongoing inflammatory process cause later clinical manifestations such as infertility.
 The immune response to many of these difficult diseases includes both humoral and cell-mediated immunity (CMI) components. The CMI response is directed to a hierarchy of T-cell antigens and epitopes from the pathogen. The epitopes are amino acid (aa) stretches of 7-9 aa (MHC I) and 12-15 aa (MHC II) (1). In chronic viral disease such as human immunodeficiency virus (HIV), and chronic bacterial disease such as TB, as well as in cancer, the hierarchy of epitope responses change over time and responses to a few immunodominant epitopes which gradually constitute a large part of the total T-cell response, whereas a large number of other epitopes that all have the potential to bind the MHC class I or II antigen presentation molecules are subdominant or even cryptic resulting in T-cell responses at levels close to or below the detection level (2-6). If induced by vaccination (without competition from dominant epitopes), responses to such subdominant epitopes have been reported to be protective (e.g., in TB (7)), indicating that the epitopes are indeed expressed during the natural infection and can be recognized by effector cells on the invading pathogen. Studies indicate a major concern for current vaccine development is that subdominant epitope responses may have advantages compared to responses to immundominant epitopes in HIV where escape mutants lack immunodominant epitopes and are therefore not seen by the immune system (8).
 The utilization of subdominant T-cell epitopes in the design of vaccines has so far been hampered by two major roadblocks: i) the need for a large panel of different epitopes to cover a diverse human population due to the variation of individual epitopes recognized by individuals with different HLA composition; ii) the need to identify subdominant epitopes to which only low-level T-cell responses close to or below the detection level of immunological assays (e.g., the enzyme-linked immunospot (ELISPOT) assay) are found.
 Olsen, et al. (7) describes that a vaccine based on one subdominant epitope of ESAT6 can protect against TB. However, a mix of overlapping peptides spanning the entire region of ESAT6 was not used in this study.
 In International Patent Application Publication No. WO 01/016163, a vaccine against virus comprising a peptide mix consisting of peptides that activate T cells regardless of their HLA genotype is described. This application teaches the use of peptide mixes from Hepatitis B to enable a broad coverage when applied for the vaccination of a genetically diverse human population thereby circumventing the non-responders found when immunizing with single peptides. This invention does not teach the peptide driven expansion of T cells directed against subdominant T-cell epitopes relevant for the preventive and therapeutic vaccination against chronic bacterial diseases as taught in the present invention.
 In International Patent Application Publication No. WO 03/011331, a prime-boost vaccine is disclosed. To prevent an increased response to dominant epitopes and decreased response to subdominant epitopes, priming is achieved by a DNA or viral vector encoding a string of epitopes. Following the priming stage, the epitopes are used individually, in separate constructs or carried on separate vehicles, to boost the response as opposed to being administered as a single poly-epitope DNA or viral construct.
SUMMARY OF THE INVENTION
 The present invention discloses a vaccine against chronic diseases such as a bacterial, viral or parasitic infection or cancer comprising a peptide mixture of overlapping peptides spanning the whole amino acid sequence of a protein that is expressed during the chronic phase of the disease such as a chronic infection caused by a bacteria, a persistent virus or parasite or from proteins expressed in malignant tumors, a method of making such vaccines and prophylaxis and treatment of chronic disease.
 The present invention use stretches of amino acid sequences, spanning a whole protein, in a peptide mixture with an overlap of 6-20 amino acids for priming and optionally boosting with the whole protein as an adjuvanted subunit vaccine or expressed in viral delivery systems for maximal induction of humoral responses as well.
 The present invention provides vaccines inducing broad recognition of dominant and subdominant responses to any given antigen. The vaccine comprises pools of overlapping fragments of the desired antigen in appropriate adjuvants. The T-cell repertoire is thereby expanded to include not only the immunodominant epitope recognized when the intact molecule is used for immunization and induced by the chronic infection itself, but also to induce a much broader and balanced response to a number of the subdominant epitopes as well. One significant advantage of the present invention is that it requires no prior knowledge of the precise identity of the subdominant epitopes and their recognition in a human population but expands the T-cell repertoire and thereby the total number of target specific T cells primed by vaccination from a few immunodominant epitopes and to multiple epitopes. The resulting T-cell response to subdominant epitopes is important for protection against chronic diseases that on their own induces a response focused only towards immunodominant epitopes. For chronic disease controlled by humoral immunity the T helper cell response primed by the peptide mix may conveniently be boosted by the full size protein for maximum induction of an antibody response as well.
 Other advantages of the invention will be apparent from the detailed description of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
 FIG. 1A provides an overview of the ESAT-6 (SEQ ID NO: 1) overlapping peptides: ESAT6-P1 (amino acids 1 to 15 of SEQ ID NO: 1); ESAT6-P2 (amino acids 7 to 21 of SEQ ID NO: 1); ESAT6-P3 (amino acids 15 to 29 of SEQ ID NO: 1); ESAT6-P4 (amino acids 21 to 35 of SEQ ID NO: 1); ESAT6-P5 (amino acids 27 to 41 of SEQ ID NO: 1); ESAT6-P6 (amino acids 33 to 47 of SEQ ID NO: 1); ESAT6-P7 (amino acids 41 to 55 of SEQ ID NO: 1); ESAT6-P8 (amino acids 47 to 61 of SEQ ID NO: 1); ESAT6-P9 (amino acids 55 to 68 of SEQ ID NO: 1); ESAT6-P10 (amino acids 61 to 74 of SEQ ID NO: 1); ESAT6-P11 (amino acids 67 to 81 of SEQ ID NO: 1); ESAT6-P12 (amino acids 74 to 88 of SEQ ID NO: 1); and ESAT6-P13 (amino acids 80 to 94 of SEQ ID NO: 1).
 FIG. 1B provides the amino acid sequence of Δ15-ESAT-6 (amino acids 16 to 94 of SEQ ID NO: 1).
 FIGS. 2A and 2B illustrate the immunogenicity of ESAT6 and Δ15ESAT6 in splenocytes. Groups of F1 (Balb/cxC57BL/6) mice were subcutaneously vaccinated three times at two-week intervals with either saline, ESAT6 (FIG. 2A) or Δ15ESAT6 (FIG. 2B) in DDA/TDB. Three weeks after the final vaccination, spleen cells were analyzed by ELISA for INF-γ secretion following stimulation with 1 microgram/ml ESAT6, Δ15ESAT6 or one of the 13 overlapping peptides covering the ESAT6 sequence (P1-P13 as indicated in the figure, also shown in FIG. 1).
 FIG. 3 shows the protective efficacy of ESAT6 and Δ15ESAT6. Groups of F1 (Balb/cxC57BL/6) mice were subcutaneously vaccinated three times at two-week intervals with either saline (column 1), BCG (column 2), ESAT6 (column 3) or Δ15ESAT6 (column 4). Six weeks after the last vaccination the mice were challenged with virulent M. tuberculosis. Six weeks post-challenge, the mice were killed and the bacterial burden (colony forming units, CFU) was measured in the lung.
 FIG. 4 provides a table of TB10.4 (SEQ ID NO: 2) with its overlapping peptides: TB10.4-P1 (amino acids 1 to 18 of SEQ ID NO: 2); TB10.4-P2 (amino acids 11 to 28 of SEQ ID NO: 2); TB10.4-P3 (amino acids 21 to 38 of SEQ ID NO: 2); TB10.4-P4 (amino acids 31 to 48 of SEQ ID NO: 2); TB10.4-P5 (amino acids 41 to 58 of SEQ ID NO: 2); TB10.4-P6 (amino acids 51 to 68 of SEQ ID NO: 2); TB10.4-P7 (amino acids 61 to 78 of SEQ ID NO: 2); TB10.4-P8 (amino acids 71 to 88 of SEQ ID NO: 2); and TB10.4-P9 (amino acids 81 to 96 of SEQ ID NO: 2).
 FIG. 5 is a bar chart showing the results of vaccination with recombinant TB10 followed by in vitro stimulation with individual peptides P1-P9. In vitro IFN-γ, responses of cells from mice vaccinated three times with DDA/TDB-TB10.4 in DDA/TDB. Cells taken two weeks after final vaccination from blood and stimulated with 0.5 μg/ml of the indicated peptide.
 FIG. 6 is a bar chart showing the recognition of TB10.4 peptides P1-P9 following vaccination with individual peptides. In vitro IFN-γ responses of cells from mice vaccinated three times with individual TB10.4 peptides in DDA/TDB. Cells taken two weeks after final vaccination from blood and stimulated with 0.5 μg/ml of the same peptide used for the vaccination and secretion of IFN-γ was determined by ELISA.
 FIG. 7 is a bar chart showing the protective ability of TB10.4 peptides P1-P9. Bacterial burden in vaccinated mice (expressed as log10 in colony forming units (CFU) protection) challenged by the aerosol route with virulent M. tuberculosis six weeks after the last vaccination. Six weeks post-challenge, the mice were killed and the bacterial burden (CFU) was measured in the lung. (* P<0.05 compared to non-vaccinated mice, ANOVA and Tukey's test).
 FIG. 8 is a bar chart showing the recognition of TB10.4 peptides P1-P9 after vaccinating with TB10.4 peptide mix. In vitro IFN-γ responses of cells from mice vaccinated three times with DDA/TDB-TB10.4-peptide mix. Cells taken two weeks after final vaccination from blood and stimulated with 0.5 μg/ml peptide or TB10.4 protein as indicated.
 FIG. 9 is a bar chart showing the bacterial burden in TB10.4 or TB10.4-peptide vaccinated mice infected with M. tuberculosis. Bacterial burden in vaccinated mice (expressed as log10 in CFU) compared to non-vaccinated controls challenged by the aerosol route with virulent M. tuberculosis ten weeks after the first vaccination. Six weeks post-challenge, the mice were killed and the bacterial burden (CFU) was measured in the lung. (* P<0.05, ANOVA and Tukey's test).
 FIG. 10 provides an overview of the CT521 (SEQ ID NO: 3) overlapping peptides: CT521-P1 (amino acids 1 to 22 of SEQ ID NO: 3); CT521-P2 (amino acids 14 to 36 of SEQ ID NO: 3); CT521-P3 (amino acids 27 to 49 of SEQ ID NO: 3); CT521-P4 (amino acids 40 to 62 of SEQ ID NO: 3); CT521-P5 (amino acids 53 to 75 of SEQ ID NO: 3); CT521-P6 (amino acids 66 to 88 of SEQ ID NO: 3); CT521-P7 (amino acids 77 to 99 of SEQ ID NO: 3); CT521-P8 (amino acids 90 to 112 of SEQ ID NO: 3); CT521-P9 (amino acids 102 to 124 of SEQ ID NO: 3); and CT521-P10 (amino acids 116 to 138 of SEQ ID NO: 3).
 FIG. 11 is a bar chart showing the release of IFN-γ in peripheral blood mononuclear lymphocytes (PBMC) cultured with ESAT-6 peptides. Mice were vaccinated three times at 2-week intervals with a mix of all the ESAT-6 peptides (P1-P 13), and the immune response as measured by secretion of IFN-γ, was investigated by culturing blood cells with each of the individual ESAT-6 peptides P1-P13.
 FIG. 12 shows the immunogenicity of a ESAT-6 and ESAT-6 peptide mix. Mice were vaccinated three times at 2-week intervals with either saline (column 1), ESAT-6 peptide mix (P1-P13; column 2), or ESAT-6 (column 3). 6 weeks after the last vaccination, the mice were subjected to an aerosol challenge with virulent M. tuberculosis 10 weeks after the challenge, the mice were killed and the bacterial numbers were determined in the lungs.
DETAILED DESCRIPTION OF THE INVENTION
 The present invention discloses a vaccine against a chronic disease such as a bacterial, viral or parasitic infection or cancer comprising a peptide mixture consisting of adjacent overlapping peptides spanning the whole amino acid sequence of a protein that is expressed during the chronic phase of the disease.
 The present invention discloses the use of a mixture of overlapping peptides derived from an antigenic protein and/or the nucleic acid encoding these peptides for a vaccine against a chronic disease such as a bacterial, viral or parasitic infection or cancer.
 The peptides are 10 to 30 amino acids long, preferably 12-20 amino acids long where the overlap with the adjacent peptide is 6-20 amino acids, and more preferably 10-12 amino acids.
 The antigenic protein which the peptide mixture spans is chosen among proteins that are expressed during the chronic phase of a disease and induces a cell mediated immune response in the case of chronic disease.
 In one embodiment, the protein is selected from a bacteria such as a virulent mycobacteria, e.g. by Mycobacterium tuberculosis, Mycobacterium africanum or Mycobacterium bovis, Mycobacterium leprae or Chlamydia trachomatis or a virus such as hepatitis B or C or a parasite such as Leishmania or the malaria causing parasite Plasmodium falciparum or from molecules expressed in malignant tumours.
 The peptides are not restricted to but preferably from a protein selected from M. tuberculosis such as ESAT6, Ag85A, Ag85B or TB10.4 or from Chlamydia trachomatis such as CT184, CT521, CT443, CT520, CT521, CT375, CT583, CT603, CT610 or CT681 or from a hepatitis B or C or from Plasmodium falciparum such as Msp1, Msp2, Msp3, Ama1, GLURP, LSA1, LSA3 or CSP.
 The invention also discloses a method for preparing a peptide mixture according to the invention by proteolytic cleavage of the protein with two or more proteolytic cleavage agents such as proteolytic enzymes such a trypsin, V-8 protease, AspN (cleaves N-terminal to aspartic acid) or chymotrypsin or chemical agents such as cyanogen bromide (CNBr) or BNPS-skatole [3-bromo-3-methyl-2-(o-nitrophenylsulfenyl)indolenine)].
 The peptide mixture according to the invention can be used for preparing a vaccine against a chronic disease such as a bacterial, viral or parasitic infection or cancer. The vaccine can optionally comprise a delivery system such as an adjuvant. The adjuvant is preferably a based on cationic liposomes such as dimethyldioctadecylammonium bromide/Trehalose dibehenate (DDA/TDB). The peptide mixture used for vaccination can be mixed with preformed liposomes or each peptide can be mixed with the preformed liposomes, the individual peptides formulated in the liposomes are then mixed before immunization.
 Each peptide in the peptide mixture can preferably be individually mixed with the liposome prior to making the peptide mixture for optimal interaction with individual antigen presenting cells from the immune system thereby ensuring maximum responses to all epitopes from the molecule.
 The invention also discloses a method and vaccine for prophylaxis or therapeutic treatment of a chronic disease in an animal, including a human being, comprising administering to the animal the vaccine of the invention. Optionally the prophylaxis or treatment is boosted by administering a second vaccine comprising the full size protein spanned by the peptide mixture in an adjuvant or expressed in a viral delivery system or as a pure DNA vaccine for optimal boosting a CMI as well as a humoral response.
 The invention further discloses a vaccine in which the amino acid sequence is lipidated or conjugated directly to TLR agonist such as CPG so as to allow a self-adjuvanting effect of the polypeptide.
 The preferred embodiment of the invention is a vaccine comprising a peptide mixture of the invention preferably with an adjuvant as described above.
 A chronic disease is a long-lasting or recurring disease. The term chronic describes the course of the disease, or its rate of onset and development. A chronic course is distinguished from a recurrent course; recurrent diseases relapse repeatedly, with periods of remission in between. Chronic infections can be caused by bacteria, e.g. Mycobacteria sp. or Chlamydia sp. among others, by virus e.g. Hepatitis or HIV, by a parasite, e.g., a malaria causing parasite or Leishmania or by diseases such as cancer, diabetes etc.
 The word "peptide" in the present invention should have its usual meaning. That is an amino acid chain of any length being a part or fragment of a protein, wherein the amino acid residues are linked by covalent peptide bonds.
 The peptide may be chemically modified by being glycosylated, by being lipidated (e.g., by chemical lipidation with palmitoyloxy succinimide as described by (9), labeling with PAM3Cys (18) or with dodecanoyl chloride as described by (10)), by comprising prosthetic groups, or by containing additional amino acids such as e.g. a his-tag or a signal peptide or by direct conjugation to TLR agonist (e.g. as described by (11)).
 Each peptide may thus be characterised by specific amino acids and be encoded by specific nucleic acid sequences. It will be understood that such sequences include analogues and variants produced by recombinant or synthetic methods wherein such polypeptide sequences have been modified by substitution, insertion, addition or deletion of one or more amino acid residues in the recombinant polypeptide and still be immunogenic in any of the biological assays described herein. Substitutions are preferably "conservative". These are defined according to the following table Amino acids in the same block in the second column and preferably in the same line in the third column may be substituted for each other. The amino acids in the third column are indicated in one-letter code.
TABLE-US-00001 ALIPHATIC Non-polar G, A, P I, L, V Polar-uncharged C, S, T, M N, Q Polar-charged D, E K, R AROMATIC H, F, W, Y
 A peptide mixture is liquid mixture of fragments of a protein.
 A preferred peptide mixture within the present invention is based on a protein from M. tuberculosis such as ESAT6, Ag85A, Ag85B or TB10.4 or from Chlamydia trachomatis such as CT184, CT521, CT443, CT520, CT521 or CT375 or from a hepatitis virus or from Plasmodium falciparuman such as momp, omp, msp1, msp3, ama1 or glurp. It may also be a peptide mixture or proteolytic digest based on a fusion molecule e.g. as previously described as a relevant vaccine constructs against TB in PCT/DK2006/000356. In general all peptide mixtures of proteins inducing a CMI response which can be used in vaccines against chronic disease can be used to induce an increased prophylactic or therapeutic response as a vaccine
 Throughout this specification, unless the context requires otherwise, the word "comprise", or variations thereof such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element or integer or group of elements or integers but not the exclusion of any other element or integer or group of elements or integers.
 Although the minimum length of a T-cell epitope has been shown to be at least 6 amino acids, it is normal that such epitopes are constituted of longer stretches of amino acids. Hence, it is preferred that the polypeptide fragment of the invention has a length of at least 7 amino acid residues, such as at least 8, at least 9, at least 10, at least 12, at least 14, at least 16, at least 18, at least 20, at least 22, at least 24, and at least 30 amino acid residues. Hence, in important embodiments of the inventive method, it is preferred that the polypeptide fragment has a length of at most 50 amino acid residues, such as at most 40, 35, 30, 25, and 20 amino acid residues. It is expected that the peptides having a length of between 10 and 20 amino acid residues will prove to be most efficient as MHC class II epitopes and therefore especially preferred lengths of the polypeptide fragment used in the inventive method are 18, such as 15, 14, 13, 12 and even 11 amino acid residues. It is expected that the peptides having a length of between 7 and 12 amino acid residues will prove to be most efficient as MHC class I epitopes and therefore especially preferred lengths of the polypeptide fragment used in the inventive method are 11, such as 10, 9, 8 and even 7 amino acid residues.
 By T cell epitopes is understood a sequence of amino acids that is recognized by specific T cells through their T cell receptor after presentation by an antigen presenting cell in the context of either MHC classI or II.
 A dominant epitope is a sequence of amino acids that, when part of a protein, induce a high T cell response and often the majority of the response to an antigen is directed to a few T dominant T cell epitopes.
 A subdominant epitope is a sequence of amino acids that when part of a protein does not induce a strong T cell response, even though the epitopes are immunogenic and able to induce a significant T cell response when isolated from the protein.
 By mixture of overlapping polypeptides or protein fragments is understood a mixture of 10 to 30 mers, with a 6-20 amino acid overlap, spanning an entire protein.
 A common feature of the polypeptides of the invention is their capability to induce an immunological response as illustrated in the examples. It is understood that a variant of a polypeptide of the invention produced by substitution, insertion, addition or deletion may also be immunogenic as determined by any of the assays described herein.
 An immune individual is defined as a person or an animal, which has cleared or controlled an infection.
 The immune response may be monitored by one of the following methods:
 An in vitro cellular response is determined by induction of the release of a relevant cytokine such as IFN-γ or the induction of proliferation in lymphocytes withdrawn from an animal or human being currently or previously infected with virulent mycobacteria or immunized with the relevant peptide mixture. The induction being performed by the addition of the peptide mixture or the immunogenic portion of the mixture to a suspension comprising from 2×105 cells to 4×105 cells per well. The cells being isolated from either the blood, the spleen, the lymph nodes, the liver or the lung and the addition of the polypeptide or the immunogenic portion resulting in a concentration of not more than 20 μg per ml suspension and the stimulation being performed from two to five days. For monitoring cell proliferation the cells are pulsed with radioactive labeled Thymidine and after 16-22 hours of incubation detecting the proliferation is measured by liquid scintillation counting. A positive response is defined as being a response more than background plus two standard deviations. The release of IFN-γ can be determined by the ELISA method, which is well known to a person skilled in the art. A positive response being a response more than background plus two standard deviations. Other cytokines than IFN-γ could be relevant when monitoring the immunological response to the polypeptide, such as IL-12, TNF-α, IL-4, IL-5, IL-10, IL-6, TGF-β. Another and more sensitive method for detecting the immune response is the ELISpot method, in which the frequency of IFN-γ producing cells is determined. In an ELlspot plate (MAHA, Millipore) precoated with anti-murine IFN-γ antibodies (PharMingen) graded numbers of cells isolated from either blood, spleen, or lung (typically between 1 to 4×105 cells/well) are incubated for 24-32 hrs in the presence of the peptide mixture or the immunogenic portion resulting in a concentration of not more than 20 μg per ml. The plates are subsequently incubated with biotinylated anti-IFN-quadrature antibodies followed by a streptavidin-alkaline phosphatase incubation. The IFN-γ producing cells are identified by adding BCIP/NBT (Sigma), the relevant substrate giving rise to spots. These spots can be enumerated using a dissection microscope. It is also a possibility to determine the presence of mRNA coding for the relevant cytokine by the use of the PCR technique. Usually one or more cytokines will be measured utilizing for example PCR, ELISPOT or ELISA. It will be appreciated by a person skilled in the art that a significant increase or decrease in the amount of any of these cytokines induced by a specific peptide mixture can be used in evaluation of the immunological activity of the polypeptide.
 An in vitro cellular response may also be determined by the use of T cell lines derived from an immune individual or an infected person where the T cell lines have been driven with either live bacteria, extracts from the bacterial cell or culture filtrate for 10 to 20 days with the addition of IL-2. The induction being performed by addition of not more than 20 μg peptide mixture per ml suspension to the T cell lines containing from 1×105 cells to 3×105 cells per well and incubation being performed from two to six days. The induction of IFN-γ or release of another relevant cytokine is detected by ELISA. The stimulation of T cells can also be monitored by detecting cell proliferation using radioactively labeled Thymidine as described above. For both assays a positive response being a response more than background plus two standard deviations.
 An in vivo cellular response may be determined as a positive delayed-type hypersensitivity (DTH) response after intradermal injection or local application patch of at most 100 μg of the polypeptide or the immunogenic portion to an individual who is clinically or subclinically infected with a virulent bacterium, a positive response having a diameter of at least 5 mm 72-96 hours after the injection or application.
 An in vitro humoral response is determined by a specific antibody response in an immune or infected individual. The presence of antibodies may be determined by an ELISA technique or a Western blot where the peptide mixture or the immunogenic portion is absorbed to either a nitrocellulose membrane or a polystyrene surface. The serum is preferably diluted in PBS from 1:10 to 1:100 and added to the absorbed peptide mixture and the incubation being performed from 1 to 12 hours. By the use of labeled secondary antibodies the presence of specific antibodies can be determined by measuring the optical density (OD), e.g., by ELISA where a positive response is a response of more than background plus two standard deviations or alternatively a visual response in a Western blot.
 Another relevant parameter is measurement of the protection in animal models induced after vaccination with the peptide mixture in an adjuvant or after DNA vaccination. Suitable animal models include primates, guinea pigs or mice, which are challenged with an infection. Readout for induced protection could be decrease of the bacterial load in target organs compared to non-vaccinated animals, prolonged survival times compared to non-vaccinated animals and diminished weight loss compared to non-vaccinated animals.
 In general, antigens and DNA sequences encoding such antigens, may be prepared using any one of a variety of procedures.
 The peptide mixture can be produced synthetically when the peptide fragment have fewer than about 100 amino acids, and generally fewer than 50 amino acids and may be generated using techniques well known to those ordinarily skilled in the art, such as commercially available solid-phase techniques where amino acids are sequentially added to a growing amino acid chain.
 In the construction and preparation of plasmid DNA encoding the peptide mixture as defined by the invention for DNA vaccination a host strain such as E. coli can be used. Plasmid DNA can then be prepared from cultures of the host strain carrying the plasmid of interest, and purified using, e.g., the QIAGEN Giga-Plasmid column kit (Qiagen, Santa Clara, Calif., USA) including an endotoxin removal step. It is preferred that plasmid DNA used for DNA vaccination is endotoxin free.
Protease Digest of Antigens
 A set of overlapping peptides can be made by proteolytic cleavage of the intact protein which can be expressed as a recombinant tagged protein in, e.g., E. coli, followed by purification by column chromatography such as metal chelate chromatography. Two or more proteolytic cleavage agents can be selected that will generate different fragments and thereby overlapping peptide cocktail. Proteolytic enzymes such as trypsin, V-8 protease, AspN or chymotrypsin can be used or chemical agents like CNBr or BNPS-skatole. The number of cleavage sites and the length of the fragments generated are determined by the amino acid sequence of the protein and the specific cleavage agent, e.g., Asp-N hydrolyzes proteins at the N-terminal side of aspartic acid and cysteic acid residues. The V-8 protease cleaves at the carboxyl side of glutamic acid in ammonium bicarbonate buffer at pH 7.8. For proteolytic enzymes coupling of the enzyme to beads before cleavage is possible (16), and this coupling will allow removal of the enzyme after completion of the cleavage by centrifugation of the beads. Alternatively, the protease can be removed from the digestion mixture by chromatographic methods such as gel filtration or reversed-phase high performance liquid chromatography (HPLC). After digestion of the protein, mass spectrometry analysis of the digest is performed to confirm that cleavage of the protein has taken place as predicted. Finally, the two digestion mixtures can be combined to form a mixture of overlapping peptides.
 A vaccination with a recombinant protein will induce a T cell response towards a limited number of dominant peptide epitopes within this protein. In contrast, vaccinating with a mix of overlapping peptides, spanning the entire amino acid sequence of the protein, will generate a T cell response against an increased number of epitopes being both dominant and sub-dominant peptide epitopes.
 The invention pertains to a vaccine composition comprising a peptide mixture according to the invention. In order to ensure optimum performance of such a vaccine composition it is preferred that it comprises an immunologically and pharmaceutically acceptable carrier, vehicle or adjuvant.
 An effective vaccine, wherein a peptide mixture of the invention is recognized by the animal, will in an animal model be able to decrease bacterial load in target organs, prolong survival times and/or diminish weight loss after challenge with an infectious organism, compared to non-vaccinated animals either when given as a preventive or therapeutic vaccine.
 Suitable vehicles are selected from the group consisting of a diluent and a suspending agent. The adjuvant is preferably selected from the group consisting of DDA, Quil A, poly I:C, aluminum hydroxide, Freund's incomplete adjuvant, IFN-γ, IL-2, IL-12, monophosphoryl lipid A (MPL), Trehalose Dimycolate (TDM), TDB and muramyl dipeptide (MDP).
 An adjuvant is defined as a substance that non-specifically enhances the immune response to an antigen. Depending on the nature of the adjuvant it can promote a cell-mediated immune response, a humoral immune response or a mixture of the two. Since the enhancement of the immune response is non-specific, it is well understood in the field that the same adjuvant can be used with different antigens to promote responses against different targets e.g. with an antigen from M. tuberculosis to promote immunity against M. tuberculosis or with an antigen derived from a tumor, to promote immunity against tumors of that specific kind.
 "Liposomes" are defined as closed vesicles structures made up of one or more lipid bilayers surrounding an aqueous core. Each lipid bilayer is composed of two lipid monolayers, each of which has a hydrophobic "tail" region and a hydrophilic "head" region. In the bilayer, the hydrophobic "tails" of the lipid monolayers orient toward the inside of the bilayer, while the hydrophilic "heads" orient toward the outside of the bilayer. Liposomes can have a variety of physicochemical properties such as size, lipid composition, surface charge, fluidity and number of bilayer membranes. According to the number of lipid bilayers liposomes can be categorized as unilamellar vesicles (UV) comprising a single lipid bilayer or multilamellar vesicles (MLV) comprising two or more concentric bilayers each separated from the next by a layer of water. Water soluble compounds are entrapped within the aqueous phases/core of the liposomes opposed to lipophilic compounds which are trapped in the core of the lipid bilayer membranes.
 The peptide mixture used for vaccination can be mixed with preformed liposomes as previously described (WO2006002642 which is hereby incorporated as reference) or each peptide can be mixed with the preformed liposomes in the same manner, the individual peptides formulated in the liposomes are then mixed before immunization.
 The standard preparation of liposomes is by dissolving the lipids in an organic solvent which is then evaporated to dryness leaving a thin lipid film on the inside of the test tube. The dry lipid film is then hydrated in an appropriate amount of aqueous phase and the mixture is heated to above the phase transition temperature of the lipids and allowed to "swell". The resulting liposomes which consist of multilamellar vesicles (MLV's) are dispersed by shaking the test tube.
 Different principles for interaction of a peptide or peptide mixtures to liposomes exist. One method is surface association (by electrostatic or hydrophobic interactions) of the peptides with the liposomes by incubation of the peptides with preformed liposomes (19). It is also possible to make a covalent coupling of peptides to the surface of the liposomes by chemical crosslinking (e.g. as described in reference 20). In addition, the peptides can be encapsulated in the liposomes by different methods. One method is to add the peptides directly into the lipid film followed by rehydration. Another method describes adding the peptides to the buffer used for rehydration of the liposomes from the lipid film. In addition, the peptides can be encapsulated by the dehydration-rehydration method (21) in which a peptide is encapsulated by freeze drying followed by rehydration of the lyophilized liposomes. Alternatively the antigen is encapsulated using the freeze and thaw technique described by Pick (22) and by Bally et al. in U.S. Pat. No. 4,975,282. In this technique vesicles are mixed with the protein antigen and repeatedly snap frozen in liquid nitrogen and warmed to temperatures above the main phase transition temperature of the relevant lipids. The vesicles may be further processed to remove any non-entrapped antigen e.g. by washing and centrifuging.
 Finally, the peptide mixture can then be delivered by the liposomes in two ways. The peptides can either be mixed before the interaction with the liposomes or the peptides can be mixed after interaction of the individual peptides with the liposomes as described above.
 The peptides can also be encapsulated in the liposomes by adding the peptides to the buffer used for rehydration of the liposomes from a lipid film or on freeze dried form.
 The polypeptide may also be chemically modified by being glycosylated, by being lipidated (e.g. by chemical lipidation with palmitoyloxy succinimide as described by Mowat et al. 1991, labeling with PAM3Cys (18) or with dodecanoyl chloride as described by Lustig et al. 1976), by comprising prosthetic groups or by direct conjugation to TLR agonist (e.g., as described by Seder 2006).
 Preparation of vaccines which contain peptide sequences as active ingredients is generally well understood in the art, as exemplified by U.S. Pat. Nos. 4,608,251; 4,601,903; 4,599,231 and 4,599,230, all incorporated herein by reference.
 Other methods of achieving adjuvant effect for the vaccine include use of agents such as aluminum hydroxide or phosphate (alum), synthetic polymers of sugars (CARBOPOL brand), aggregation of the protein in the vaccine by heat treatment, aggregation by reactivating with pepsin treated (Fab) antibodies to albumin, mixture with bacterial cells such as C. parvum or endotoxins or lipopolysaccharide components of gram-negative bacteria, emulsion in physiologically acceptable oil vehicles such as mannide mono-oleate (Aracel A) or emulsion with 20 percent solution of a perfluorocarbon (Fluosol-DA) used as a block substitute may also be employed. Other possibilities involve the use of immune modulating substances such as cytokines or synthetic IFN-γ inducers such as poly I:C in combination with the above-mentioned adjuvants.
 Another interesting possibility for achieving adjuvant effect is to employ the technique described in (17) (which is hereby incorporated by reference herein). In brief, a relevant antigen such as an antigen of the present invention can be conjugated to an antibody (or antigen binding antibody fragment) against the Fcγ receptors on monocytes/macrophages.
 The vaccines are administered in a manner compatible with the dosage formulation, and in such amount as will be therapeutically effective and immunogenic. The quantity to be administered depends on the subject to be treated-, including, e.g., the capacity of the individual's immune system to mount an immune response, and the degree of protection desired. Suitable dosage ranges are of the order of several hundred micrograms active ingredient per vaccination with a preferred range from about 0.1 μg to 1000 μg, such as in the range from about 1 μg to 300 μg, and especially in the range from about 10 μg to 50 μg. Suitable regimens for initial administration and booster shots are also variable but are typified by an initial administration followed by subsequent inoculations or other administrations.
 The manner of application may be varied widely. Any of the conventional methods for administration of a vaccine are applicable. These are believed to include oral application on a solid physiologically acceptable base or in a physiologically acceptable dispersion, parenterally, by injection or the like. The dosage of the vaccine will depend on the route of administration and will vary according to the age of the person to be vaccinated and, to a lesser degree, the size of the person to be vaccinated.
 The vaccines are conventionally administered parenterally, by injection, for example, either subcutaneously or intramuscularly. Additional formulations which are suitable for other modes of administration include suppositories and, in some cases, oral formulations. For suppositories, traditional binders and carriers may include, for example, polyalkalene glycols or triglycerides; such suppositories may be formed from mixtures containing the active ingredient in the range of 0.5% to 10%, preferably 1-2%. Oral formulations include such normally employed excipients as, for example, pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, and the like. These compositions take the form of solutions, suspensions, tablets, pills, capsules, sustained release formulations or powders and advantageously contain 10-95% of active ingredient, preferably 25-70%.
 In many instances, it will be necessary to have multiple administrations of the vaccine. Especially, vaccines can be administered to prevent an infection. When administered to prevent an infection, the vaccine is given prophylactically, before definitive clinical signs or symptoms of an infection are present. Since the current vaccines, e.g., BCG appears to induce an effective, but short-lived immune response, prophylactic vaccines may also be designed to be used as booster vaccines. Such vaccines are given to individuals who have previously received a vaccination, with the intention of prolonging the period of protection.
 In instances where the individual has already become infected or is suspected to have become infected, the previous vaccination may have provided sufficient immunity to prevent primary disease, but as discussed previously, boosting this immune response will not help against the latent infection. In such a situation, the vaccine has a particular advantage as a therapeutic vaccine designed for efficacy against the latent stage of infection.
 Importantly in chronic diseases such as TB, cancer, hepatitis and HIV, the long term equilibrium between host and pathogen often results in immune responses focused towards a few immuno-dominant epitopes. Inducing a broad balanced response towards a range of epitopes within a given protein can not be achieved by immunizing with the recombinant protein, which would only lead to a response towards a limited number of dominant epitopes. However, in contrast, the present invention teaches that vaccinating with a mix of overlapping peptides does induce a T cell immune response towards a range of epitopes within a given protein. The present invention and the induction of responses to subdominant epitopes therefore are particularly advantageous for these diseases because it can induce an immune response against protective epitopes that are not induced by the chronic disease, or by vaccinating with the given protein in a recombinant full length form. By conventional preventive vaccination or post-exposure in a therapeutic manner the application of the peptide mixture vaccine technology is superior and with much higher activity than conventional vaccines based on full size molecules against these chronic diseases.
 Furthermore, for chronic diseases where humoral immunity is important, it is possible to induce an optimal broad T cell response and a maximal B cell response towards the same protein. In this situation, primary immunization is done with a mix of overlapping peptides (in an adjuvant) spanning the entire sequence of a given protein and the boosting is achieved with a second vaccine comprising the same protein in recombinant form in an adjuvant. In this way the broad T cell response against both dominant and subdominant epitopes will enable maximal T helper cell activity and thereby a very strong antibody response. The resulting response is a broad T cell and maximal antibody response towards the same antigen, with particular use against chronic diseases.
 The following examples are illustrative only and do not limit the scope of the invention.
 The degree to which the Mycobacterium tuberculosis-expressed antigen ESAT-6 contains dominant and subdominant epitopes was examined as follows. Mice were vaccinated with the recombinant protein ESAT-6 3 times at 2 weeks interval and cells were taken two weeks after final vaccination from blood and stimulated with the indicated ESAT-6 peptides (FIG. 1A) [SEQ ID NO:1]. After stimulation, secretion of interferon gamma (IFN-γ), as assessed by ELISA, was determined. The results showed an induction of IFN-γ producing T cells specific for P1 (amino acids 1 to 15 of SEQ ID NO: 1) and to a lesser degree P2 (amino acids 7 to 21 of SEQ ID NO: 1). Removing the immunodominant epitope P1 from ESAT6 (giving the construct named "Δ15-ESAT-6 in which the amino acids 1-15 of ESAT 6 (SEQ ID NO:1) have been deleted" (FIG. 1B)) led to immune recognition of new epitopes, P2 and in particular P3 (FIG. 2). This demonstrated that P1 is a dominant epitope, and that P2 and P3 (amino acids 15 to 29 of SEQ ID NO: 1) constitute subdominant (but immunogenic) epitopes.
 Next, whether the subdominant epitopes were able to confer protection against infection with M. tuberculosis was examined. Mice were subcutaneously vaccinated three times at two-week intervals with either saline, BCG, DDA/TDB with ESAT6, or Δ15ESAT6. Six weeks after the last vaccination the mice were challenged with virulent M. tuberculosis. Six weeks post-challenge, the mice were killed and the bacterial burden (CFU) was measured in the lung.
 Protection experiments showed that Δ15-ESAT-6 was more protective than ESAT-6 (FIG. 3), indicating that the subdominant peptides (epitopes) P2 and P3 were indeed able to induce an immune response that mediated protection against infection with M. tuberculosis.
 Next, whether vaccination with a mix of all overlapping ESAT-6 peptides would lead to a broader recognition of P1-P13 compared to mice vaccinated with the recombinant protein ESAT-6 was examined. Mice were vaccinated three times at 2-week intervals with a mix of all the peptides, and the immune response was investigated by culturing blood cells with each of the individual ESAT-6 peptides P1-P13 (FIG. 11). The results showed that, in contrast to vaccinating with recombinant protein ESAT-6, vaccinating with a mix of ESAT-6 peptides (P1-P13) led to a broader recognition of the peptides (FIG. 11).
 To examine whether the broader response towards ESAT-6 was reflected in the protection against infection with M. tuberculosis, as compared to the protein induced by vaccination with the recombinant protein ESAT-6, mice were vaccinated three times at 2-week intervals with either ESAT-6 or ESAT-6-peptide mix. 6 weeks after the last vaccination, the mice were subjected to an aerosol challenge with virulent M. tuberculosis 10 weeks after the challenge, the mice were killed and the bacterial numbers were determined in the lungs.
 The results showed that mice vaccinated with ESAT-6 peptide mix not only exhibited a broader recognition of ESAT-6, but were also significant more protected against infection with M. tuberculosis compared to mice vaccinated with the recombinant protein ESAT-6 (FIG. 12). Thus, vaccinating with a mix of ESAT-6 peptides leads to a broader recognition of ESAT-6 epitopes which in turn induce a significant higher protection against infection with M. tuberculosis, compared to when vaccinating with the recombinant protein ESAT-6.
 Another protein expressed by M. tuberculosis TB 10.4 was analyzed as follows. Mice were vaccinated 3 times at 2 weeks interval with recombinant TB10.4, and cells were taken two weeks after final vaccination from blood and stimulated with 0.5 μg/ml of the indicated TB10.4 peptides (FIG. 4, SEQ ID NO:2) and secretion of IFN-gamma (IFN-γ), as assessed by ELISA, was determined. The results showed that vaccinating with TB10.4 mainly induced P3 specific T cells (FIG. 5). P3 therefore constituted a dominant epitope.
 To analyze whether the lack of T cells responding to peptides P1 (amino acids 1 to 18 of SEQ ID NO: 2), P2 (amino acids 11 to 28 of SEQ ID NO: 2), P4 (amino acids 31 to 48 of SEQ ID NO: 2), P5 (amino acids 41 to 58 of SEQ ID NO: 2), P6 (amino acids 51 to 68 of SEQ ID NO: 2), and P9 (amino acids 81 to 96 of SEQ ID NO: 2) (and to some degree P7 (amino acids 61 to 78 of SEQ ID NO: 2) and P8 (amino acids 71 to 88 of SEQ ID NO: 2)) was due to these peptide epitopes being subdominant or not immunogenic, animals were vaccinated with the individual TB10.4 peptides (P1-P9). Following vaccination purified lymphocytes were stimulated in vitro the same peptides used for vaccination and secretion of IFN-γ was determined by ELISA. The results showed that other, subdominant (when vaccinating with the recombinant protein TB10.4) peptides were also strongly immunogenic. In particular vaccinating with peptide 1 or 3, or to a lesser degree P7, P8, or P9 induced a specific T-cell response (FIG. 6).
 In addition, the subdominant peptides, in particular P1, P7, P8, P9 all protected against infection with M. tuberculosis (FIG. 7). Vaccinating with the dominant peptide epitope P3 (amino acids 21 to 38 of SEQ ID NO: 2) also induced significant protection.
 Having determined the existence of subdominant epitopes when vaccinating with the recombinant protein TB10.4, whether vaccination with a mix of all overlapping TB10.4 peptides would lead to a broader recognition of P1-P9 compared to mice vaccinated with the recombinant protein TB10.4 was examined. Mice were vaccinated three times at 2-week intervals with a mix of all the peptides, and the immune response was investigated by culturing blood cells with each of the individual TB10.4 peptides P1-P9 (FIG. 8).
 The results showed that, in contrast to vaccinating with recombinant protein TB10.4, vaccinating with a mix of TB10.4 peptides (P1-P9) led to a much broader recognition of the peptides. In particular, P1 (amino acids 1 to 18 of SEQ ID NO: 2), P3 (amino acids 21 to 38 of SEQ ID NO: 2), and P8 (amino acids 71 to 88 of SEQ ID NO: 2) were all strongly recognized (FIG. 8).
 To examine whether the broader response towards TB10.4 was reflected in the protection against infection with M. tuberculosis, as compared to the protein induced by vaccination with the recombinant protein TB10.4 [SEQ ID NO:2], mice were vaccinated three times at 2-week intervals with either TB10.4 or TB10.4-peptide mix. 6 weeks after the last vaccination, the mice were subjected to an aerosol challenge with virulent M. tuberculosis 6 weeks after the challenge, the mice were killed and the bacterial numbers were determined in the lungs.
 The results showed that mice vaccinated with TB10.4-peptide mix not only exhibited a broader recognition of TB10.4, but were also significant more protected against infection with M. tuberculosis compared to mice vaccinated with the recombinant protein TB10.4 (FIG. 9). Thus, vaccinating with a mix of TB10.4 peptides leads to a broader recognition of TB10.4 epitopes which in turn induce a significant higher protection against infection with M. tuberculosis, compared to when vaccinating with the recombinant protein TB10.4 [SEQ ID NO:2].
 Mice were vaccinated 3 times at 2 weeks interval with recombinant CT521 or a mix of CT521 overlapping peptides (FIG. 10), and cells taken two weeks after final vaccination from blood was stimulated with 0.5 ug/ml of each of the CT521 peptides. Secretion of IFN-gamma, as assessed by ELISA, was determined to examine whether vaccinating with a mix of CT521 peptides leads to a broader recognition of CT521, compared to vaccinating with the recombinant CT521 protein.
 1. Paul, W. 1999. Fundamental Immunology, fourth edition, Lippincott-Raven.  2. Sette, A., and J. Fikes. 2003. Curr Opin Immunol 15:461.  3. van der Most, R. G., K. Murali-Krishna, J. G. Lanier, E. J. Wherry, M. T. Puglielli, J. N. Blattman, A. Sette, and R. Ahmed. 2003. Virology 315:93.  4. Crowe, S. R., S. J. Turner, S. C. Miller, A. D. Roberts, R. A. Rappolo, P. C. Doherty, K. H. Ely, and D. L. Woodland. 2003. J Exp Med 198:399.  5. Wherry, E. J., J. N. Blattman, K. Murali-Krishna, R. van der Most, and R. Ahmed 2003. J Virol 77:4911.  6. Kamath, A. B., J. Woodworth, X. Xiong, C. Taylor, Y. Weng, and S. M. Behar. 2004. J Exp Med 200:1479.  7. Olsen, A. W., P. R. Hansen, A. Holm, and P. Andersen. 2000. Eur J Immunol 30:1724.  8. McMichael, A. J., and R. E. Phillips. 1997. Annu Rev Immunol 15:271.  9. Mowat et al 1991, Immunology 72(3):317-22  10. Lustig et al 1976, Cell Immunol 24(1):164-7  11. Wille-Reece, U., C. Y. Wu, B. J. Flynn, R. M. Kedl, and R. A. Seder. 2005. J. Immunol. 174:7676.6  12. Thompson J., et al Nucleic Acids Res 1994 22:4673-4680  13. Ravn, P. et al 1999. J. Infect. Dis. 179:637-645  14. Stryhn, A., et al 1996 Eur. J. Immunol. 26:1911-1918  15. Harboe, M., et al 1998 Infect. Immun. 66:2; 717-723  16. Krogh, T N, Berg, T, & Hojrup, P. (1999). Anal. Biochem. 274, 153-162  17. Gosselin et al., 1992. J. Immunol. 149: 3477-3481  18. Babu et al. 1995. Vaccine 13:1669-76.  19. Davidsen et al (2005). Biochim Biophys Acta. 1718: 22-31.  20. Munoz et al (2004). Int J Pharm 269:177-84.  21. Kirby & Gregoriadis. 1984. 2: 979-984.  22. Pick U. 1981. Arch. Biochem. Biophys. 212: 186-194.
 All documents cited herein are incorporated by reference. Modification to the embodiments illustrated herein will be appreciated by one of skill in the art and are within the scope of the invention as recited in the following claims.
3194PRTMycobacterium tuberculosis 1Met Thr Glu Gln Gln Trp Asn Phe Ala Gly Ile Glu Ala Ala Ala Ser1 5 10 15Ala Ile Gln Gly Asn Val Thr Ser Ile His Ser Leu Leu Asp Glu Gly 20 25 30Lys Gln Ser Leu Thr Lys Leu Ala Ala Ala Trp Gly Gly Ser Gly Ser 35 40 45Glu Ala Tyr Gln Gly Val Gln Gln Lys Trp Asp Ala Thr Thr Glu Leu 50 55 60Asn Asn Ala Leu Gln Asn Leu Ala Arg Thr Ile Ser Glu Ala Gly Gln65 70 75 80Ala Met Ala Ser Thr Glu Gly Asn Val Thr Gly Met Phe Ala 85 90297PRTMycobacterium tuberculosis 2Met Ser Gln Ile Met Tyr Asn Tyr Pro Ala Met Leu Gly His Ala Gly1 5 10 15Asp Met Ala Gly Tyr Ala Gly Thr Leu Gln Ser Leu Gly Ala Glu Ile 20 25 30Ala Val Glu Gln Ala Ala Leu Gln Ser Ala Trp Gln Gly Asp Thr Gly 35 40 45Ile Thr Tyr Gln Ala Trp Gln Ala Gln Trp Asn Gln Ala Met Glu Asp 50 55 60Leu Val Arg Ala Tyr His Ala Met Ser Ser Thr His Glu Ala Asn Thr65 70 75 80Met Ala Met Met Ala Arg Asp Thr Ala Glu Ala Ala Lys Trp Gly Gly 85 90 95Glx3138PRTChlamydia trachomatis 3Met Leu Met Pro Lys Arg Thr Lys Phe Arg Lys Gln Gln Lys Gly Gln1 5 10 15Phe Ala Gly Leu Ser Lys Gly Ala Thr Phe Val Asp Phe Gly Glu Phe 20 25 30Gly Met Gln Thr Leu Glu Arg Gly Trp Ile Thr Ser Arg Gln Ile Glu 35 40 45Ala Cys Arg Val Ala Ile Asn Arg Tyr Leu Lys Arg Lys Gly Lys Val 50 55 60Trp Ile Arg Val Phe Pro Asp Lys Ser Val Thr Lys Lys Pro Ala Glu65 70 75 80Thr Arg Met Gly Lys Gly Lys Gly Ala Pro Asp His Trp Val Val Val 85 90 95Val Arg Pro Gly Arg Ile Leu Phe Glu Val Ala Asn Val Ser Lys Glu 100 105 110Asp Ala Gln Asp Ala Leu Arg Arg Ala Ala Ala Lys Leu Gly Ile Arg 115 120 125Thr Arg Phe Val Lys Arg Val Glu Arg Val 130 135
Patent applications by Peter Andersen, Bronshoj DK
Patent applications by STATENS SERUM INSTITUT
Patent applications in class Liposomes
Patent applications in all subclasses Liposomes