EP3328422A1

EP3328422A1 - Vaccine composition against chlamydiaceae infections

Info

Publication number: EP3328422A1
Application number: EP16753280.3A
Authority: EP
Inventors: Philippe Verbeke; Colette Kanellopoulos
Original assignee: Centre National de la Recherche Scientifique CNRS; Institut National de la Sante et de la Recherche Medicale INSERM; Universite Paris Diderot Paris 7
Current assignee: Centre National de la Recherche Scientifique CNRS; Institut National de la Sante et de la Recherche Medicale INSERM; Universite Paris Diderot Paris 7
Priority date: 2015-07-28
Filing date: 2016-07-28
Publication date: 2018-06-06
Also published as: US20200384098A1; US20220160861A1; US10695416B2; US11865169B2; US20180214536A1; FR3039406B1; US11229691B2; WO2017017221A1; FR3039406A1

Abstract

The invention relates to vaccine compositions for treating and/or preventing infections by a bacterium of the Chlamydiaceae family, said compositions comprising bacteria of the Chlamydiaceae family, which have been previously treated by at least one peptidoglycan inhibitor, or extracts of said treated bacteria.

Description

VACCINE COMPOSITION AGAINST CHLAMYDIACEAE INFECTIONS

INTRODUCTION

Infections with bacteria of the family Chlamydiaceae, which can affect humans or animals, are responsible for a range of particularly serious pathologies.

Chlamydia is the most common sexually transmitted disease of bacterial origin with nearly 106 million new cases a year. Effective antibiotic treatments exist but this disease is often asymptomatic (75% of women and 50% of men). Most patients are not treated because they are undiagnosed and the consequences of untreated infection can be serious (infertility, ectopic pregnancies, preterm births, neonatal infections).

Thus, the development of a vaccine is a major health issue in order to eradicate the disease.

There is currently no effective vaccine to prevent Chlamydia infections in humans. Different vaccination strategies have been conducted over the last twenty years, but problems of low immunogenicity (antigenic vaccines, inactivated forms) or regulatory (live attenuated forms that can be reactivated) have not allowed these vaccines to be tested in the clinical phase.

The family Chlamydiaceae comprises two genera, Chlamydia and Chlamydophila, each comprising several species; each species consists of different biovars and serovars. Each of these species leads to a set of disabling diseases in humans or animals, or even fatal in the case of C. psittaci infections.

The bacteria of the family Chlamydiaceae are Gram-negative bacteria. They are called "strict intracellular" because they can only grow and multiply in a parasitophorous vacuole within an infected eukaryotic cell. During their development, bacteria of the family Chlamydiaceae come in two forms: • The elementary body (EC), which is the infectious form and does not divide, and

• The cross-linked body (CR), non-infectious, strictly intracellular and divided by binary fission.

The CE enters the host cell within a gallbladder. If several ECs infect the same cell, the vesicles usually cluster at the centrosome and merge with each other to form the inclusion. After 5 to 12 hours of infection, ECs differentiate into CRs that actively multiply. After 30 to 40 hours, the CRs become EC; the inclusion and the host cell are then lysed, releasing the bacterial offspring that will infect the neighboring cells. All of these parameters may vary from one serovar and one bacterial species to another, and depending on the experimental conditions (Fields, K. A. & T. Hackstadt, Annu Rev Cell Dev Biol 18: 221-45, 2002).

During its development cycle, the bacterium sets up many strategies to survive in the host cell. The Chlamydia bacterium notably inhibits the apoptosis of the host cell induced by external signals, inhibits the fusion of lysosomes with bacterial inclusion, defeats the vesicular traffic towards the vacuole to allow the growth of this one, and injects into the cytoplasm multiple virulence factors, including a key protease (Chlamydia protease / proteasome-like activity factor, CPAF) that induces the degradation of many eukaryotic proteins, transcription factors of the major histocompatibility complex molecules responsible for the presentation of antigens to the cells of the immune system.

To these mechanisms developed during a continuous bacterial cycle is added the phenomenon of persistence. In response to certain stresses in the cellular environment, such as the presence of certain antibiotics or interferon gamma (IFN-gamma) or the absence of iron, the bacterium stops its bacterial cycle and its proliferative mechanism, thus becoming a persistent body, viable but not culturable in vitro. Persistence accounts for a high level of interaction between the pathogen and the host and allows the bacteria to remain alive, or dormant ("persistent") in the body for months or years. Indeed, although it is very difficult to demonstrate the persistence in vivo, multiple studies suggest that a Chlamydia bacteria can exist for several years within a tissue such as the genital tract, conjunctival mucosa or vascular tissue, thus generating recurrent infections and chronic inflammation (Beatty et al., Microbiol Rev 58 (4): 686-99, 1994; Kern et al. ., FEMS Immunol Med Microbiol 55 (2): 131-9, 2009). The high rate of asymptomatic infections and the severity of the diseases justify the active search for a safe and effective vaccine for the control of Chlamydia infections. To date, some 40 vaccine trials have been carried out mainly in the mouse, using either inactivated bacteria or purified antigens or recombinant antigenic proteins, or even DNA vaccines (see for example Hafner et al., Vaccine, 32). (14): 1563-1571, 2014, Farris et al., Infection and Immunity, 79: 986-996, 201 1, Schautteet et al., Infect Dis., Obstet Gynecol., 201: 963513, 201 1; Campos et al., In Vision and Ophthalmology, 36 (8) 1477-1491, WO 92/00096, Lu Hang et al., The Journal of Immunology, 169 (11), 6324-6331). None gave convincing results. It is agreed that an attenuated form of the bacterium could be the basis of an excellent vaccine. Unfortunately Chlamydiaceae can not be transformed and very few experimentally attenuated strains have been isolated.

Currently no vaccine exists on the market to prevent Chlamydiaceae infections in humans. The asymptomatic nature of a large number of infections by bacteria of the family Chlamydiaceae and the severity of the pathologies developed justify the search for a safe and effective preventive vaccine, that is to say which has a high immunogenicity all guaranteeing a low risk of infection by the subject.

The inventors have found that, very surprisingly and contrary to established prejudices, the forms of Chlamydiaceae inactivated by a peptidoglycan inhibitor, in particular β-lactams or D-cycloserine, can be used very efficiently to produce drugs for prophylactic treatment of infections by bacteria of the family Chlamydiaceae.

DESCRIPTION OF THE INVENTION The inventors have previously shown that the treatment of cell cultures infected with bacteria of the Chlamydiaceae family by peptidoglycan inhibitors, in particular by β-lactams, leads to the formation of forms. bacterial abnormalities, BL forms, which lost all infectivity (WO 201 1/086134, Dumoux et al., PLoS One 8 (12): e8351 1, 2013). These results were later confirmed by other laboratories. (Ouellette et al., Mol Microbiol 85 (1): 164-178, 2012; Pilhofer et al., Nat Commun., 4: 2856, 2013; Liechti et al., Nature 506 (7489): 507-510; 2014). The inventors have now found that, quite surprisingly, the BL forms always have native antigens, even though these forms are abnormally dilated and are absolutely no longer infectious. The injection of BL forms into mice thus makes it possible to protect these animals against subsequent infections by infectious bacteria. This BL form therefore represents an inactivated form that can be used to immunize naive individuals susceptible to infection by Chlamydiaceae.

The inventors have shown that the BL form obtained by treatment of bacteria of the family Chlamydiaceae by a peptidoglycan inhibitor, in particular by a β-lactam, is immunogenic. The term "immunogen" as used herein refers to the ability of a molecule to elicit an immune response, whether humoral or cell-mediated, or both. An immune response to an immunogenic bacterial form, as understood herein, means the development in a subject of a humoral and / or cell-mediated immune response to one or more molecules present in said bacterial form (e.g., an antigen, as a protein, a glycolipid (LPS) or a polysaccharide). The term "humoral immune response" is understood to mean an immune reaction whose effectors are soluble molecules, for example antibodies. These are in particular produced by plasma cells and B lymphocytes. A "cell-mediated immune response" within the meaning of the invention is an immune reaction whose effectors are cells such as cytotoxic T lymphocytes, killer T cells or helper T cells. A "cell-mediated immune response" within the meaning of the invention also includes the production of cytokines, chemokines and other similar molecules produced by activated T cells and / or other hematopoietic cells, including those derived from CD4 ⁺ T cells. or CD8 ⁺ , and / or epithelial cells. The ability of a particular antigen or bacterial form to stimulate a cell-mediated immune response can be readily determined by those skilled in the art. There exists in the art a large number of tests for this purpose (see, for example, Erickson et al. , J. Immunol. 51: 4189-4199, 1993; Doe et al. , fur. J. Immunol. 24: 2369-2376, 1994).

In particular, the BL form of the present invention is capable of eliciting an immune response of antibody-producing B lymphocytes and Chlamydia-specific T-lymphocytes (LT) in the spleen. In response to intravaginal Chlamydia infection, these LT effector effectors (effector or regulators) are likely to leave the spleen for the ganglia draining the genital tract where the infection occurs.

According to a first aspect, the subject of the invention is a vaccine composition comprising bacteria of the family Chlamydiaceae previously treated with at least one peptidoglycan inhibitor, in particular with a β-lactam, or extracts thereof for use in prophylactic and / or therapeutic treatment of infections by bacteria of the family Chlamydiaceae.

For the purposes of the invention, the term "Chlamydiaceae family" is intended to mean the taxonomic group composed of two genera, Chlamydia and Chlamydophila, as defined in Bush & Everett, Int J Syst Evol Microbiol. 51 (Pt 1): 203-20, 2001. Similarly, "genus Chlamydia" means, within the meaning of the invention, the taxonomic group comprising the species Chlamydia trachomatis, Chlamydia suis and Chlamydia muridarum, and by "genus Chamydophila", the taxonomic group composed of the species Chlamydophila abortus, Chlamydophila psittaci, Chlamydophila caviae, Chlamydophila pecorum, Chlamydophila felis and Chlamydophila pneumoniae (Bush & Everett, Int J Syst Evol Microbiol, 51 (Pt 1): 203-20, 2001). It is well known to those skilled in the art that these species have distinct host spectra: for example, Chlamydia trachomatis and Chlamydophila pneumoniae are responsible for infections in humans, Chlamydia suis in pigs and Chlamydophila abortus in humans. ruminants. The invention is not limited to a specific bacterial species, but can be applied to any of the species of the family Chlamydiaceae and, in particular, to those mentioned above.

Various adjuvants are commonly used in the manufacture of vaccine compositions to increase immunogenicity, for example by stimulating the immune system. For the purposes of the invention, the term "adjuvant" describes any substance added to accelerate, prolong, enhance or modify the quality of the specific immune response induced by the composition according to the invention when the adjuvant and the composition according to the invention are used together. Adjuvants are thus products that enhance innate and adaptive immune system responses when administered in the presence of antigens of viral, bacterial or synthetic origin. They cause the massive attraction of macrophages at the injection site, then in the lymph nodes, activate dendritic cells, increase the production of specific immunoglobulins, antibodies, and stimulate many cells involved in the mechanisms of immune defense. Thus, according to a particular embodiment, the composition according to the invention further comprises a pharmaceutically acceptable adjuvant. The pharmaceutically acceptable adjuvants are well known to those skilled in the art and may be chosen according to the proper and interesting properties of these adjuvants, such as those described by Petrovsky et al. , Immunology and Cell Biology, 82: 488-496, 2004 or Vermout et al. , Ann. Med. Vet. 147: 393-401, 2003. It is well known, moreover, that adjuvants of immunity can be adapted in particular according to the route of administration chosen.

The adjuvant according to the invention will, for example, be chosen from bacterial constituents, bacterial toxins, oily adjuvants, mineral adjuvants, CpG oligodeoxynucleotides, saponins, vesicular or nanoparticulate adjuvants, synthetic copolymers, lipophilic amines, cytokines, imidazoquinolones, or polysaccharides.

Among the bacterial constituents that can be used as adjuvants according to the invention, mention will be made, for example, of: Bacillus Calmette-Guerin or BCG, which comprises a strain of Mycobacterium bovis attenuated

Muramyl dipeptide (N-acetylmuramyl-1-alanyl-D-isoglutamine) or MPD, as well as its synthetic derivatives

- Trehalose dimycolate or TMD

- The endotoxin of gram-negative bacteria, also called lipolysaccharide or LPS and its derivative monophosphoryl lipid A or MPL. Among the bacterial toxins that can be used as adjuvants according to the invention, mention will be made by way of illustration:

- The cholera toxin of Vibrio cholerae (CT), in particular its purified subunit B (CTB).

- Pertussis toxin from Bordetella pertussis (PT) in inactivated form

- The thermolabile lymphotoxin of Escherichia coli (LT)

Among the oily adjuvants that can be used as adjuvants according to the invention, mention will be made by way of illustration:

Oil adjuvants based on squalene such as for example TiterMax (marketed under this name by Vaxcel Norcross Georgia USA) or RIBI Adjuvant System (product marketed under this name by Ribi Immunochem Research, Hamilton, Montana USA).

Among the inorganic adjuvants that can be used as adjuvants according to the invention, mention may be made, by way of example, of alum, a name commonly used to designate compounds such as aluminum hydroxide and aluminum phosphate, potassium phosphate or calcium phosphate.

Among the saponins that can be used as adjuvants according to the invention, mention may be made by way of example of those extracted from the Quillaja saponaria molina bark (Quil A), preferentially the purified forms QS-21 and QS-7 (see for reference Kensil and Dev Biol Stand, 92: 41 -7, 1998).

Among the synthetic copolymers that may be used as adjuvants according to the invention, mention may be made by way of example of synthetic amphipathic copolymers composed of hydrophilic chains of polyoxyethylene (POE) and hydrophobic chains of polyoxypropylene (POP) or dimethyldioctadecylammonium bromide or chloride (DDA). ).

Among the lipophilic amines which can be used as adjuvants according to the invention, mention may be made by way of example of avridine.

Cytokines useful as adjuvants according to the invention include, for example, histamine, interferon, in particular INF ?, interleukins, in particular IL-1 and IL-2. Among the imidazolquinolones that may be used as adjuvants according to the invention, mention may be made, by way of example, of imiquimod or resiquimod.

Among the polysaccharides that may be used as adjuvants according to the invention, mention may be made, by way of example, of dextrans, mannan, glucans and chitosan. According to the invention, the adjuvant is, for example, hevea, TASO3 (composed of squalene, DL-α-tocopherol, and polysorbate), MF59C.1 (composed of polysorbate 80, squalene, sorbitan trioleate, sodium citrate, citric acid and water).

The inventors have discovered that, surprisingly, the bacteria of the Chlamydiaceae family treated with peptidoglycan inhibitors, in particular with β-lactams, as well as the fragments of these bacteria, are highly immunogenic. In fact, the vaccine compositions comprising these inactivated bacteria induce very good protection of mice against vaginal infections by Chlamydia muridarum. In particular, the inventors have shown that the repeated administration of the vaccine compositions of the invention results in an immune response of Chlamydia muridarum-specific T lymphocytes in the spleen. In response to intravaginal infection with Chlamydia muridarum, these activated CD4 + and CD8 + LTs and regulatory T cells (CD4 + FoxP3 +) leave the spleen for the ganglia draining the genital tract.

The term "T cells" or "T lymphocytes" is used here to mean a type of lymphocyte that plays a central role in cell-mediated immunity. T cells can be distinguished from other lymphocytes, such as B cells and natural killer cells (NK cells), by the presence of a T cell receptor (TCR) on the cell surface. A "T cell receptor" or "TCR" as used herein is a receptor present on the surface of T cells that is responsible for the specific recognition of antigens presented by the major histocompatibility complex (MHC) molecules. There are CD4 + T lymphocytes that express the CD4 glycoprotein on their surface, CD8 + T cells characterized by the expression of the CD8 glycoprotein. A "T effector lymphocyte" within the meaning of the invention is a T lymphocyte providing a specialized function in the immune response, such as the secretion of cytokines or the assistance to B cells in humoral function (CD4 + T lymphocytes also called lymphocytes T helper) as well as a cytotoxic activity (CD8 + T lymphocytes). Over-expressed (ICOS, CD44) or under-expressed (CD62L) surface markers mark the activation status of effector T cells. "Regulatory lymphocytes" within the meaning of the invention are T cells which strongly express markers of the CD4 and CD25 surface. These cells also express the FOXP3 marker which is a transcription factor (Battaglia and Rancarolo 2009). These regulatory lymphocytes are therefore CD4 + CD25highFOXP3high. These cells are characterized by an ability to suppress or downregulate immune responses mediated by effector T cells, such as CD4 + or CD8 + effector.

According to a second aspect, the present invention relates to a process for preparing a vaccine composition for the prophylactic and / or therapeutic treatment of infections by bacteria of the family Chlamydiaceae, said method comprising a contacting step, in vitro, bacteria, preferably intracellular bacteria of the family Chlamydiaceae with at least one peptidoglycan inhibitor, including at least one β-lactam. For the purposes of the invention, the term "peptidoglycan inhibitor" is intended to mean any compound capable of inhibiting the synthesis of the peptidoglycan or of affecting the structure thereof. The peptidoglycan inhibitors within the meaning of the invention include, among others, D-cycloserine (d-4-amino-3-isoxazolidinone), vancomycin, teicoplanin, bacitracin, daptomycin and β-lactams. A "peptidoglycan inhibitor" within the meaning of the invention is preferably D-cycloserine or a β-lactamine.

By β-lactam is meant herein any antibiotic which contains a β-lactam nucleus in its molecular structure. Bis-lactams within the meaning of the invention are thus understood to include penicillin derivatives as well as cephalosporins, monobactams, carbapenems or β-lactamase inhibitors. In particular, the β-lactam of the invention may be benzylpenicillin (penicillin G), phenoxymethylpenicillin (penicillin V), ampicillin (penicillin A), benzyl benzylpenicillin, methicillin, dicloxacillin, flucloxacillin, co - amoxiclav (amoxycillin + clavulanic acid), piperacillin, ticarcillin, azlocillin, carbenicillin, cephalexin, cephalothin, cephazolin, cefaclor, cefuroxime, cefamandole, cefotetan, cloxacillin, cephadroxil, cefixime , cefoxitin, ceftriaxone, cefotaxime, ceftazidime, cefepime, cefpirome, imipenem, imipenem in combination with cilastatin, cefixime in combination with imipenem, meropenem, mecillinam, ertapenem , aztreonam, clavulanic acid, tazobactam or sulbactam. In a preferred aspect of the invention, said β-lactam is not amoxicillin. According to a more preferred embodiment of the invention, said β-lactam is chosen from the group consisting of benzylpenicillin (penicillin G), phenoxymethylpenicillin (penicillin V), cloxacillin, cephadroxil, cefixime, imipenem, cefixime in combination with imipenem, mecillinam, clavulanic acid, tazobactam and sulbactam. In an even more preferred embodiment, said β-lactam is penicillin G. Those skilled in the art can easily determine the conditions of treatment of bacteria with peptidoglycan inhibitors, particularly with β-lactams, which make it possible to obtain BL forms that are used in the vaccine composition. The effect of β-lactams on the phenotype of Chlamydiaceae in particular has been known since the 1970s. Generally speaking, those skilled in the art will be able to rely on the teaching of the publications of the inventors, as well as those of the other laboratories having shown an effect of β-lactams on Chlamydiaceae (WO 201 1/086134, Dumoux et al., PLoS One 8 (12): e8351 1, 2013, Ouellette et al., Mol Microbiol 85 (1): 164-178 2012, Pilhofer et al., Nat Commun 4: 2856, 2013, Liechti et al., Nature 506 (7489): 507-510, 2014). In particular, the concentration of peptidoglycan inhibitor, especially 6 lactam, to be used to obtain the BL forms can be easily evaluated based on the publications of the prior art, including the publications of the inventors.

For example, a concentration of at least 100 μl, preferably at least 200 μl, of D-cycloserine makes it possible to generate BL forms.

According to a particular embodiment of the invention, the β-lactam is used at a concentration greater than or equal to 0.1 μΜ, preferably greater than or equal to 0.3 μΜ. According to a first variant of the invention, cephadroxil or sulbactam is used at a concentration greater than or equal to 3 μΜ, preferably greater than or equal to 10 μΜ. According to another variant of the invention, cefixime and imipenem are used in combination, each at a concentration greater than or equal to 30 μM. According to the particular aspect of the invention, cefixime or imipenem is used at a concentration greater than or equal to 100 μΜ, preferably greater than or equal to 300 μΜ. According to a particular embodiment of the invention, the mecillinam is used at a concentration greater than or equal to 1 μΜ, preferably greater than or equal to 3 μΜ. According to another embodiment of the invention, tazobactam is used at a concentration greater than or equal to 10 μΜ, preferably greater than or equal to 30 μΜ. According to a particular aspect of the invention, clavulanic acid is used at a concentration greater than or equal to 0.3 μΜ, preferably greater than or equal to 1 μΜ. According to a particularly advantageous variant of the invention, amoxicillin, benzylpenicillin (penicillin G), phenoxymethylpenicillin (penicillin V), cloxacillin or mecillinam, is used at a concentration greater than or equal to 0.1 μΜ, preferably greater than or equal to equal to 0.3 μΜ.

Similarly, one skilled in the art will be able to appreciate the incubation time of the bacteria with peptidoglycan inhibitors, especially the 6-lactamines, necessary for the appearance of BL forms. It may for example follow the appearance of such forms under the microscope. As explained above, it will also be able to consult the publications of the prior art.

It is thus particularly advantageous to incubate the bacteria with said peptidoglycan inhibitors, including β-lactam antibiotics, during the complete development time of the bacterial inclusion, that is to say until it fills 80 to 90% of the cell volume. According to a preferred embodiment of the invention, the bacteria of the family Chlamydiaceae are brought into contact with said inhibitor for at least 1 hour, preferably at least 2 hours, more preferably at least 3 hours, even more preferably at least 4 hours. hours, still more preferably at least 5 hours, even more preferably at least 10 hours, more and more preferably at least 24 hours. Bacteria of the family Chlamydiaceae exist in different forms, depending on the phase of their life cycle. The virulent form of these bacteria is the elemental body. This is suitable for survival in the external environment, with no possibility of multiplication but with the ability to penetrate, probably by phagocytosis, within the host cell. In the vacuole, the elementary body is transformed into a reticulated body, a larger element whose DNA is decondensed and which can multiply to give elementary bodies which will then be released into the medium. The inventors have shown that the bacteria are particularly sensitive to peptidoglycan inhibitors, especially to β-lactams, after having infected eukaryotic cells. Said bacteria are then in the form of crosslinked bodies which express the target enzymes of these inhibitors, which are essential for the biosynthesis of a molecule regulating bacterial division. Advantageously, said bacteria of the invention are treated with said inhibitor, for example with a 6-lactam, after these bacteria have infected eukaryotic cells. In this case, it is advantageous in the vaccine composition to use a cell lysate of the infected eukaryotic cell, said lysate comprising said bacteria treated with 6-lactamine.

In this preferred embodiment, the subject of the present invention is a process for the preparation of a composition for the prophylactic and / or therapeutic treatment of infections by bacteria of the family Chlamydiaceae, said method comprising the steps of: contacting eukaryotic cells in vitro with bacteria of the Chlamydiaceae family, and obtaining infected eukaryotic cells; b) incubating the infected eukaryotic cells obtained in step a) with at least one peptidoglycan inhibitor, in particular at least one 6-lactamine;

c) preparation of a lysate of the cells of step b).

According to the invention, steps a) and b) of the process for preparing the vaccine composition are carried out under conventional cell culture conditions and which are well known to a person skilled in the art, who will be able to choose and adapt them according to the type of eukaryotic cell used. Preferentially, steps a) and b) are carried out at a temperature of 37 ° C., an air humidity of 35% and an air CO 2 content of 5%. According to the invention the cells are cultured in a culture medium appropriate. According to one aspect of the invention, the incubation of step b) is maintained for at least one hour, preferably at least 2 hours, more preferably at least 3 hours, even more preferably at least 4 hours, still more preferably at less than 5 hours, even more preferably at least 10 hours, more and more preferably at least 24 hours.

The eukaryotic cells according to the invention are animal cells, preferably mammalian cells or avian cells. The latter are for example cells of the order Galliformes, such as chicken (Gallus gallus) or that of the Anseriformes, such as mallard duck (Anas platyrhynchos) or musk duck (Cairina moschata). The mammalian cells according to the invention are, for example, eukaryotic cells derived from rodents (Rodentiens), porcine eukaryotic cells (Suidae), or eukaryotic primate cells. The eukaryotic rodent cells are, for example, of the family Muridae (Muridae), in which there are among others the subfamilies of hamsters (Cricetinae) or mice and rats (Murinae), which include, for example, the mouse (mus musculus) or the rat (rattus norvegicus). Porcine eukaryotic cells include, among others, eukaryotic cells of domestic swine (Sus scrofa domesticus). The eukaryotic cells of the order of the primates comprise, inter alia, eukaryotic cells of the family Cercopithecidae, in which mention will be made, for example, of the green monkey (Chlorocebus sabaeus), or that of Hominidae, which includes, in particular, the human (Homo sapiens). However, eukaryotic cells within the meaning of the present invention do not include cells whose production requires or has required the destruction of human embryos. According to one embodiment of the invention, the eukaryotic cells are primary cells or immortalized or tumor cell lines, such as, for example, eukaryotic cells from cell lines. "Primary cells" are defined as a group of original cells derived from normal tissue up to and including the 10th passage, used for the production of biological products. For the purposes of the invention, the term "immortalized cells" is intended to mean cells that divide beyond the Hayflick limit, the cells being able to be immortalized spontaneously or because of the implementation of an immortalization technique. The immortalization techniques of the cells are well known to those skilled in the art who will be able to choose among them the best adapted to their goal. By way of example, and without limiting the invention to these examples, mention may be made, as an immortalization technique, of the transformation with an oncogene, for example those encoding the SV40 T antigen, the Ras protein or the Myc protein. or the Abl protein, or the overexpression of a telomerase reverse transcriptase, for example hTERT, or the culture of eukaryotic cells at confluence during several passages. The eukaryotic cells used are chosen for example from epithelial cells or fibroblates. Thus, according to one embodiment of the invention, the eukaryotic cells used are, by way of example, primary fibroblasts of embryonic origin, such as, for example, CEFs (Chick Embryo Fibroblast), REF (Rat Embryo Fibroblasts) or MEF (Mouse Embryo Fibroblast). It is also possible to use avian stem cell lines, as described in WO 2008/129058). Preferably, the eukaryotic cells according to the invention come from cell lines. According to an advantageous embodiment, the eukaryotic cells according to the invention come from one of the lines chosen from the immortalized cell lines NIH3T3, Vero, COS-7, the tumor lines Caco-2, CHO, PC12, HeLa, Jurkat, HL- 60, AtT20, GH3, HEK-293, HT29, HT-29, LNCap, MCF-7, MDA-MB-231, MDCK, Saos-2, Sf9, Sf21, S2, T-47D, U20S and EB66® lines. (Valneva, France). These cells are commonly used by laboratories working in the field. They are available from cell culture collections such as the ATCC (American Type Culture Collection) or DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen), or commercially. Those skilled in the art will be able to choose, if necessary, the eukaryotic cells according to the invention as a function of the bacterium used or else according to the subject for whom the composition according to the invention is intended. The whole bacteria can be used as an immunogen in the vaccine composition of the invention, once they have been treated with said peptidoglycan inhibitor, especially a β-lactam. However, those skilled in the art will readily understand that extracts of the bacteria thus treated can also be used in said vaccine composition, as long as said extracts have intact native antigens. According to a first embodiment, said extract is a membrane extract. According to another embodiment, the extract is a cytoplasmic extract. Protocols for isolating membrane extracts have been described in the art (see, for example, Frohlich et al., J. Microbiol Methods 91 (2): 222-230, 2012) and can be used to obtain such extracts. They include two steps, a nitrogen cavitation first and a second immunoprecipitation with antibodies against LPS bacteria of the family Chlamydiaceae.

Nitrogen cavitation allows eukaryotic cells to be lysed in a gentle manner without abrupt increase in temperature in the sample (Gottlieb & Adachi, Methods Enzymol 322: 213-221, 2000). Advantageously, some eukaryotic cell debris is removed by low speed centrifugation (between 3000 g and 6000 g), while the bacteria remain in the supernatant. In a preferred embodiment, the method of the invention will therefore comprise an additional step of low speed centrifugation between the nitrogen cavitation step and the immunoprecipitation step with antibodies against LPS of the bacteria of the family of Chlamydiaceae. Gentle sonication in the ice can be used as well.

Antibodies against LPS (or anti-MOMP, anti-InC, anti-PMP or anti-CPAF ... antibodies) of the Chlamydiaceae family have been described in the prior art (Herrera et al., Mol. Med. 9: 135-142, 2003). They make it possible to selectively isolate the bacterial membrane fraction in the immunoprecipitation step after lysing the eukaryotic cells while the bacterial cytoplasmic fraction remains in the supernatant.

It may be advantageous to enrich the bacterial fraction by subjecting the lysates freed of cell debris to centrifugation to separate the remaining bacterial membrane fraction in the supernatant of the particulate fraction that precipitates. Preferably, the lysates are centrifuged at a rate of between 10,000 and 20,000 g, more preferably between 12,000 g and 18,000 g, still more preferably between 14,000 g and 17,000 g, and most preferably between 15,000 g and 16,000 g. The cytoplasmic extracts can be obtained by subjecting the pellet to isopycnic ultracentrifugation, according to the conditions described by Frohlich et al. (J Microbiol Methods 91 (2): 222-230, 2012). As shown by the results of the inventors, the vaccine compositions of the invention are particularly useful for preventing or treating infections by bacteria of the family Chlamydiaceae, as well as pathologies caused by said infections. The vaccine compositions of the invention are particularly capable of triggering a specific immune reaction against bacteria of the family Chlamydiaceae. This reaction is characterized in particular by an immune response of T-lymphocytes specific for Chlamydia muridarum in the spleen. In response to an intravaginal infection with Chlamydia muridarum, these activated CD4 + and CD8 + LTs and regulatory T cells leave the spleen for the ganglia draining the genital tract. As shown by the results reported in the examples (see in particular Examples 3 and A), this immune response is capable of protecting the individual against bacteria of the family Chlamydiaceae. According to a third aspect, the invention therefore also relates to bacteria of the family Chlamydiaceae and / or extracts thereof characterized in that said bacteria have been previously treated with at least one peptidoglycan inhibitor, especially at least one a β-lactam for their use in the prophylactic or therapeutic treatment of infections by bacteria of the family Chlamydiaceae.

The invention also relates to the use of a composition comprising bacteria of the family Chlamydiaceae and / or extracts thereof characterized in that said bacteria have been previously treated with a peptidoglycan inhibitor, especially at least one β-lactam, for the manufacture of a medicament for the prophylactic or therapeutic treatment of infections of bacteria of the family Chlamydiaceae. In the same way, the invention also relates to a method of treatment, preferably prophylactic, of infections by bacteria of the family Chlamydiaceae by a composition comprising bacteria of the family Chlamydiaceae and / or extracts thereof, said bacteria having been previously treated with a peptidoglycan inhibitor, especially at least one β-lactam. According to a particular embodiment, said method of treatment comprises a step of administering said composition to a subject likely to be infected by bacteria. Preferentially, this administration results in an increase in the population of activated specific CD4 + and CD8 + T lymphocytes activated in the spleen and their migration to the ganglia draining the infected genital tract. Alternately, according to another preferred embodiment, this administration results in a decrease in the population of regulatory T lymphocytes in the spleen and an increase in the ganglia draining the infected genital tract. More preferably, this administration results in an increase in the activated specific effector CD4 + and CD8 + T cell population and their migration to the genital tract draining ganglia and a decrease in the regulatory T cell population in the spleen and an increase in the ganglia draining the infected genital tract.

By "infection with a bacterium of the family Chlamydiaceae" or "infection with a Chlamydiaceae" means the presence in at least one cell of the body of the patient or the animal of said bacterium family Chlamydiaceae. The infection can be genital, ocular, respiratory or pulmonary; it can also affect other sites, such as vascular endothelium or joints.

Although many of the infections caused by bacteria of the family Chlamydiaceae are asymptomatic, said infections can nevertheless cause serious pathologies in patients or animals. By "pathology caused by infection with bacteria of the family Chlamydiaceae" is meant within the meaning of the invention any disease whose triggering is directly or indirectly caused by infection with at least one bacterium of the family Chlamydiaceae.

Thus included in the pathologies caused by infection by bacteria of the family Chlamydiaceae in the sense of the invention pathologies caused by Chlamydia suis, Chlamydia muridarum, Abortus, Chlamydophila psittaci, Chlamydophila caviae, Chlamydophila pecorum and Chlamydophila felis. Chlamydiaceae in the sense of the invention are thus more particularly included in abortions and neonatal mortalities caused by Chlamydophila abortus, as well as conjunctivitis, keratoconjunctivitis, purulent rhinitis, enteritis, bronchopneumonia. and pneumonia, caused especially in pigs by Chlamydia suis. In humans, these pathologies can in particular be genital pathologies or ocular pathologies or trachoma inducing blindness (Chlamydia trachomatis), but they can also be respiratory pathologies (neonatal pneumonitis). Thus it is known that Chlamydophila pneumoniae infections cause a form of pneumonia and that Chlamydophila psittaci is responsible for psittacosis. It is also known that infections by bacteria of the family Chlamydiaceae disseminate in the body causing many infections and atypical pathologies such as cardiovascular and circulatory dysfunctions (atheroma). Among the cardiovascular and circulatory dysfunctions caused by the bacteria of the family Chlamydiaceae, there may be mentioned respectively valvular stenosis and atheroma. On the other hand, said bacteria of the family Chlamydiaceae can also cause inflammatory diseases and joint diseases. It is known in particular that these bacteria can cause severe arthritis.

However, in a preferred embodiment of the invention, the pathologies caused by infection with bacteria of the family Chlamydiaceae are ocular pathologies or genital pathologies. In a more particularly preferred aspect of the invention, ocular pathologies caused by infection with bacteria of the family Chlamydiaceae include trachoma. In another particularly preferred aspect, genital pathologies caused by infection with bacteria of the family Chlamydiaceae include lymphogranuloma venereum or Durand-Nicolas-Favre disease. According to yet another particularly preferred aspect of the invention, genital pathologies in humans caused by infection with bacteria of the family Chlamydiaceae include pathologies such as urethritis and orchi-epididymitis. These can lead to a decrease in male fertility. According to yet another particularly preferred aspect of the invention, an infection by bacteria of the family Chlamydiaceae cause in the female genital pathologies such as cervico-vaginitis, cervicitis, endocervites, urethritis, endometritis or peri-hepatitis, which can lead to complications such as high genital infections and, in particular, salpingitis that can evolve, among other things, towards the formation of pyosalpinx and hydrosalpinx, which cause total obstruction of the fallopian tubes. Salpingitis is the main risk factor for tubal infertility and ectopic pregnancy in women.

It is well known to those skilled in the art that the incidence of infections is generally inversely correlated with the state of health of the patient, and that the risk infection is therefore greater in individuals who are already infected with other microorganisms. The compositions furthermore comprising other active ingredients, or a mixture of active principles, thus allow a better protection of the general health of the subjects, and consequently a better protection against infections by the bacteria of the family Chlamydiaceae.

Thus, according to a particularly advantageous variant of the invention, the composition further comprises another active ingredient. By way of example, this other active ingredient is, within the meaning of the invention, another vaccine composition.

Among the other vaccine compositions according to the invention, mention may in particular be made of vaccine compositions that may reduce the risk of pneumococcal infections, tetanus, polio, influenza, diphtheria, pertussis, hepatitis B, hepatitis A, HPV (Human papilloma virus), tuberculosis (for example by Bacille Calmette Guerin). More preferably, said other vaccine composition is capable of increasing, in vaccinated individuals, the amplitude and speed of the protective immune response.

Those skilled in the art will also be able to choose the best routes and modes of administration of the composition according to the invention, as well as optimal dosages and galenic forms, according to the criteria generally taken into account in the manufacture of a medicament or the establishment of a pharmaceutical or veterinary treatment. Preferably, these compounds will be administered systemically, in particular intravenously, intramuscularly, intradermally, intraperitoneally or subcutaneously, orally, or topically (by means of gel, aerosols, drops, etc. .). it will be particularly advantageous according to the invention to administer the composition enterally, orally, parenterally (for example subcutaneous, intradermal, or intramuscular) or mucosal (eg intranasal, sublingual, intravaginal, transcutaneous). More preferably, the pharmaceutical composition of the invention will be administered repeatedly, spread over time. Its mode of administration, its dosage and its optimal dosage form can be determined according to the criteria generally taken into account in the establishment of a treatment adapted to a patient such as the age or the body weight of the patient, the gravity general condition, tolerance to treatment and side effects noted. The composition according to the invention is prepared in any galenical form known to those skilled in the art, for example in liquid or gel form, such as solutions, suspensions, syrups, or in the form of a spray, or in solid form, such as in the form of tablets, microspheres, or capsules. Advantageously, the composition according to the invention is prepared in the form of a solution or an injectable suspension. According to a variant of the invention, the composition is freeze-dried in order to be supplied or prepared in solid form.

The solution according to the invention is administered at a therapeutically effective dose, in particular at an immunogenic dose that is to say capable of inducing an antigen-specific immune response. The antigen-specific immune response can be measured by any technique known to those skilled in the art. By way of example, the antigen-specific immune response is evaluated by measuring the concentration of antibodies (immunoglobulins or Ig) specific for the bacterium of the family Chlamydiaceae used, in the subject, in particular IgM, IgG and IgA, at a given time after the last administration of the composition, by Elisa or Elispot test. The antigen-specific immune response is evaluated from biological samples of the subject, such as, for example, blood, serum, tears or vaginal secretions.

The person skilled in the art will be able to adapt the administration dose of the composition according to the invention as a function, for example, of the chosen route of administration, the vaccination schedule, as well as the characteristics of the subject, such as the species, the age, weight, general health. According to one embodiment, the composition according to the invention is administered according to a vaccination scheme comprising several administrations. For example, according to one embodiment, the composition is administered repeatedly between 2 and 4 times over a period of 15 to 90 days, and then one or more booster administrations are carried out between 1 and 10 years from the first administration. .

Depending on the dosage form and the desired type of administration, the composition according to the invention further comprises at least one pharmaceutically acceptable excipient. By way of example, the composition according to the invention may further comprise diluents, such as sodium, calcium carbonate, or lactose, for example, lubricating agents, such as, for example, magnesium stearate, dyes, flavoring agents, texturizing agents, antibiotics, for example thimerosal or antibiotics of the β-lactam family, proteins, in particular albumin or ovalbumin, stabilizers, such as monosodium glutamate (MSG) and 2-phenoxyethanol. According to a fourth aspect of the invention, it also relates to a method for in vitro diagnosis of infection with a bacterium of the family Chlamydiaceae in a subject, comprising the steps of: a) contacting a sample of said subject with a bacterium of the family Chlamydiaceae previously treated with at least one peptidoglycan inhibitor, in particular a β-lactam, and

b) determining the presence of antibodies in said sample which are capable of binding to said bacterium.

Such methods are well known to those skilled in the art and can be implemented using a large number of standard procedures, such as radioactivity, fluorescence, luminescence, chemiluminescence, absorbance detection. , or by microscopy, imaging, etc. Thus, according to a preferred embodiment of the invention, said method comprises the steps of: a) bringing said sample into contact with specific antibodies of said bacterium generated against said bacterium previously treated with a peptidoglycan inhibitor, especially a β lactamine, said antibodies comprising a label producing a detectable signal, or being attached to a detectably labeled reagent;

b) allowing the bacterium present in said sample to bind to it so as to

form antigen / antibody complexes; and

c) determining the presence of said bacterium in said sample by means of said detectable marker.

According to a fifth aspect, the invention relates to a diagnostic kit for the detection of infection with a bacterium of the Chlamydiaceae family, comprising said bacterium previously treated with a peptidoglycan inhibitor, in particular a β-lactamine, together with substances for performing a humoral immunity determination assay against said bacterium, in a unit packing container. The diagnostic kits according to the invention include without limitation the kits for immunological methods such as immunohistochemistry, ELISA (Enzyme-Linked Immunosorbent Assay), "western blotting", immunoenzymometry, immunofluorometry, immunoluminometry, immunoradiometry ( IRMA), ΕΜΙΤ (Enzyme Multiplied Immunoassay Technique), lateral flow immunoassay, dipstick tests, immuno histo / cyto-chemistry and all other tests that are known to those skilled in the art. These immunological methods make it possible to determine the presence or absence of an antibody in a sample. They also make it possible to measure the amount of said antibody in the sample. The invention therefore also provides, according to a sixth aspect, the use of a bacterium of the family Chlamydiaceae previously treated with a peptidoglycan inhibitor, especially a β-lactam, as an in vitro diagnostic reagent in a binding, optionally in a diagnostic kit, for the detection of neutralizing antibodies conferring immunity against said bacterium. It also relates to the use of antibodies specific for a bacterium of the family Chlamydiaceae generated against said bacterium previously treated with a peptidoglycan inhibitor, especially a β-lactam, as an in vitro diagnostic reagent in a binding assay , possibly in a diagnostic kit, for the detection of said bacterium. In addition to the foregoing, the present invention also includes other features and advantages which will emerge from the examples which follow, and which should be considered as illustrating the invention without limiting its scope.

LEGENDS OF FIGURES

Figure 1: Vaccine efficacy of BL forms. BL forms result in a significant decrease in the number of infected mice.

Figure 2: Proportion of animals from different immunization groups (Mefs, b-Lac, b-Lac / 3, De) with vaginal loss of Chlamydia muridarum at different times after infection. °: p <0.08; * p <0.05; ** p <0.01; *** p <0.005 compared to the Mefs group (Mann Whitney test). Figure 3: A-Characterization of cell loss at the lamina propria of the uterine horns of mice, uterine horn normal grade 0, (A), grade 1 (B), grade 2 (C), grade 3 (D), snapshots taken at 10X magnification. B-Evaluation of the severity of the microscopic involvement of the uterine horns of the animals of the different groups. Normal uterine horn (grade 0, A), grade 1 (B), grade 2 (C), grade 3 (D). * p = 0.054 (Mann Whitney test). 4: Total number of splenic lymphocytes of the mice after complete immunization by the vaccine or control forms. The isolated cells were counted on Malassez's slide and their number was related to the number of viable cells analyzed by flow cytometry thanks to a viability marker (BD Biosciences). Representative graph of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. The symbol "ns" or the absence of stars indicates the absence of statistically significant differences between the group of control animals immunized with sonicate of uninfected MEF cells and the group of control animals injected with PBS alone, or between MEF and b-Lac groups, or MEF and De. Figure 5: Number of total CD4 ⁺ T lymphocytes, and activated after complete immunization by the vaccine forms. The total number of CD4 ⁺ T lymphocytes (A) as well as the number of CD4 + T lymphocytes exhibiting activation markers are shown by focusing on the membrane expression of CD25 (B), CD44 ^hl CD62L ^10W (C) , ICOS ⁺ (D) and the intracellular expression of FoxP3 to highlight the regulatory T cell population (E). Graphs representative of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. Unpaired t-test: the symbols *, **, represent the measurements of the p values resulting from the tests carried out with respect to the MEF control (* p <0.05, ** p <0.01,). The symbol "ns" or the absence of stars indicates the absence of statistically significant differences between the group of control animals immunized with sonicate of uninfected MEF cells and the group of control animals injected with PBS alone, or between the MEF and b-Lac groups, or MEF and De.

Figure 6: Number of total CD8 ⁺ T lymphocytes, and activated after complete immunization by the vaccine forms. The total number of CD8 ⁺ T cells (A), as well as the number of CD8 + T lymphocytes exhibiting activation markers are shown by focusing on the membrane expression of ICOS (B), and CD44 ^hl CD62L ^10W ( VS). Graphs representative of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. Unpaired t-test: the symbols *, represent the measurements of the p values resulting from the tests carried out with respect to the MEF control (* p <0.05,). The symbol "ns" or the absence of stars indicates the absence of statistically significant differences between the group of control animals immunized with sonicate of uninfected MEF cells and the group of control animals injected with PBS alone, or between the MEF and b-Lac groups, or MEF and De.

Figure 7: Total number of cells in the ganglia and spleen of mice after complete immunization with the vaccine forms, and one week post-intravaginal infection with Chlamydia muridarum. The isolated cells were counted on Malassez's slide and their number was related to the number of viable cells analyzed by flow cytometry thanks to a viability marker (BD Biosciences). Graphs representative of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. Unpaired t-test: The symbols *, **, represent the measurements of p values from MEF testing (* p <0.05, ** p <0.01,). The symbol "ns" or the absence of stars indicates the absence of statistically significant differences between the group of control animals immunized with sonicate of uninfected MEF cells and the group of control animals injected with PBS alone, or between the MEF and b-Lac groups, or MEF and De. Figure 8: Number of total CD4 ⁺ and CD8 ⁺ T splenic lymphocytes, and activated after complete immunization with the vaccine forms and one week after intra-vaginal Chlamydia infection muridarum. The total number of CD4 ⁺ (A) and CD8 ⁺ (D) T lymphocytes and their activation profile are here represented by looking at the number of CD25 ⁺ T cells among the CD4 ⁺ T (B) and CD8 ⁺ T T cells. (E), and the number of CD4 ⁺ T and CD8 ⁺ CD44 ^hi CD62L ^10W T cells (C and F, respectively). Graphs representative of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. Unpaired t-test: the symbols *, **, represent the measurements of the p values resulting from the tests carried out with respect to the MEF control (* p <0.05, ** p <0.01,). The symbol "ns" or the absence of stars indicates the absence of statistically significant differences between the group of control animals immunized with sonicate of uninfected MEF cells and the group of control animals injected with PBS alone, or between the MEF and b-Lac groups, or MEF and De. Figure 9: Number of total CD4 ⁺ ganglion T lymphocytes and CD8 ⁺ T cells, and activated after complete immunization by the vaccine forms and one week post-intravaginal infection with Chlamydia muridarum. The total number of CD4 ⁺ (A) and CD8 ⁺ (E) T lymphocytes, as well as their activation profile, are here represented by focusing on the CD4 + CD25 ⁺ (C) and ICOS ⁺ (D) lymphocyte population, and to the number of CD4 ⁺ T lymphocytes and CD8 ⁺ CD44 ^hi CD62L ^10W (B and F respectively). Graphs representative of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. Unpaired t-test: the symbols *, **, represent the measurements of the p values resulting from the tests carried out with respect to the MEF control (* p <0.05, ** p <0.01,). The symbol "ns" or the absence of stars indicates the absence of statistically significant differences between the group of control animals immunized with sonicate of uninfected MEF cells and the group of control animals injected with PBS alone, or between the MEF and b-Lac groups, or MEF and De. Figure 10: The number of proliferating CD4 ⁺ and CD8 ⁺ T lymphocytes in the ganglia draining the genital tract and the spleen after complete immunization with the vaccine forms and one week intravaginal post-infection with Chlamydia muridarum. The total number of proliferating CD4 ⁺ (A) and CD8 ⁺ (B) T lymphocytes in the ganglia draining the genital tract (I) and the spleen (II) is presented here. Graphs representative of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. Unpaired t-test: The "ns" symbol or absence of stars indicates no statistically significant differences between the group of control animals immunized with uninfected MEF sonicate and the group of control animals injected with PBS alone, or between the MEF and b-Lac groups, or MEF and De.

Figure 1 1: Number of total and proliferating CD4 ⁺ regulatory T lymphocytes in the ganglia draining the genital tract and the spleen after complete immunization by the vaccine forms and one week post-infection. The total number of total regulatory (T) and proliferative (B) regulatory CD4 ⁺ (T) lymphocytes in the ganglia draining the genital tract (I) and the spleen (II) is presented here. Graphs representative of an experiment on groups of animals individually tested (PBS, n = 3, MEF, n = 4, b-Lac, n = 5, De, n = 5). Means +/- SEM. Unpaired t-test: The symbols represent the measurements of the p values from the tests performed with respect to the MEF control (* p <0.05,). The symbol "ns" or the absence of stars indicates the absence of statistically significant differences between the group of control animals immunized with sonicated uninfected MEF cells and the group of control animals injected with PBS alone, or between the MEF and b-Lac groups, or MEF and De EXAMPLES

Example 1 Immunization of C57BL / 6J mice.

C57BL / 6J mice were vaccinated with different compositions and then secondarily infected with bacteria of the family Chlamydiaceae.

In order to avoid an immune reaction of the host linked to the recognition of alloantigens carried by eukaryotic cells, the different bacterial forms (infectious, BL) were produced in embryonic fibroblasts from C57BL / 6J mice.

For this purpose, embryonic fibroblasts (MEF) from C57BI / 6 mice with Chlamydia muridarum (Cm) were infected in vitro. This strain is genetically very close to Chlamydia trachomatis. It infects the mouse and the guinea-pig but not the human species, and causes the same physiopathological sequelae in the genital tract as in humans.

Several compositions have been prepared

C1 -composition comprising an infectious form of Cm or also called virulent form (72 h in vitro cell infection and removal of the cell lysate)

- C2- composition comprising an inactivated infectious form 30 min at 56 ° C or also called heated form (idem 1 followed by a step of inactivation by heat)

- C3- composition comprising a form inactivated by antibiotics:

(In vitro cell infection of 3h, followed by continuous incubation of infected cells with penicillin G (100IU / ml), collection of the cell lysate after 90h). This form is a BL form and in particular a b-Lac form.

It was verified by titration that form 1 was infectious, and forms 2 and 3 were not. 4 groups of 8 week old female C57BL / 6J mice were used.

Three groups were injected intraperitoneally (IP) one or more times with one of the compositions, and then the 4 groups were infected vaginally with the infectious form of Cm. The amount of composition used for each injection corresponded to about 10 cm ² of cells (MEF) cultured in vitro, 100% infected, in a volume of 150 μΙ by IP injection.

- group 1 (4 animals): infection with Cm (1 million IFU).

group 2 (3 mice): an IP injection (at the time to) of the form 1 of the bacterium. At t0 + 39j, vaginal infection with 1 million IFU of Cm.

group 3 (3 mice): three IP injections (to, to + 10j, to + 21 j) of the form 2 of the bacterium. At t + 39j, vaginal infection with 1 million IFU of Cm.

group 4 (4 mice): three IP injections (to, to + 10j, to + 21 j) of the form 3 of the bacterium. At t + 39j, vaginal infection with 1 million IFU of Cm.

After infection, the mice were kept isolated for 82 days, without any antibiotic treatment, in order to allow pathophysiological sequelae to develop. The mice were then sacrificed and examined: macroscopic appearance of the genital tract, search for tissue lesions (hydrosalpinx, deformities, fluid cysts,), measurement of the weight of the spleen, removal of various organs (including para-aortic lymph nodes draining uterus) for further analysis. Results obtained:

Group 1: 3/4 of the mice had tissue lesions of the upper genital tract on at least one of the 2 uterine horns (spleen 106 +/- 3g, normal para-aortic lymph nodes)

Group 2: 1/3 of the mice had tissue lesions of the upper genital tract on at least one of the 2 uterine horns (spleen 14 +/-

9g, normal para-aortic lymph nodes) Group 3: 2/3 of the mice had tissue lesions of the upper genital tract on at least one of the uterine horns (280 +/- 81 g spleen, normal para-aortic lymph nodes). A mouse was sacrificed 60 days after infection because it had skin wounds and significant weight loss, potentially unrelated to experience.

Group 4: no mice had tissue damage of the upper genital tract (111 +/- 17g spleen, normal para-aortic lymph nodes)

This preliminary study shows that only the group of mice preinjected with the BL form of Cm was protected from the development of tissue lesions of the high genital tract following infection with Cm.

Example 2: Vaccine Efficacy of BL Forms

In order to confirm the vaccine efficacy of the BL forms, a new experiment was carried out under the same conditions as in Example 1.

• Mouse 1 -10: immunization by MEFs at D0, D10 and D21

o Mouse 1 -5: infection with 2.10 ⁶ IFU at day 39

^■ 3/5 mice (60%) show sequelae (tissue damage of the genital tract)

o Mouse 6-10: infection with 2.10 ⁵ IFU at day 39

^■ 3/5 mice (60%) show sequelae (tissue damage of the genital tract)

• Mouse 11 -20: immunization with the previously inactivated infectious form 10 min at 90 ° C on D0, D10 and D21

o Mouse 11-15: infection with 2.10 ⁶ IFU at day 39

^■ 3/5 mice (60%) show sequelae (tissue damage of the genital tract)

o Mouse 16-20: infection with 2.10 ⁵ IFU at day 39

^■ 3/5 mice (60%) show sequelae (tissue damage of the genital tract)

• Mouse 21-30: immunization with BL form at D0, D10 and D21

o Mouse 21 -25: infection with 2.10 ⁶ IFU at day 39

^■ 0/5 mice (0%) have sequelae (tissue damage of the upper genital tract)

Mouse 26-30: infection with 2.10 ⁵ IFU at day 39 ^■ 0/5 mice (0%) have sequelae (tissue damage of the upper genital tract)

• Mouse 31 -40: immunization with the infectious form Cm at D0, D10 and D21

o Mouse 31 -35: infection with 2.10 ⁶ IFU at day 39

^■ 2/5 mice died 1 week after infection

^■ 2/3 surviving mice have sequelae (tissue lesions of the upper genital tract

o Mouse 36-40: infection with 2.10 ⁵ IFU at day 39

^■ 2/5 mice died 1 week after infection

^■ 2/3 surviving mice have sequelae (tissue damage of the upper genital tract)

The results show a significant decrease in the number of mice infected in the group previously immunized with the BL form (FIG. 1). These results confirm that administration of the BL form protects mice from C. muridarum infection.

EXAMPLE 3 Effect of Intraperitoneal Injection of Different Immunizing Doses of B-Lac Forms (BL Forms, Treated with a B-Lactamine) or Pc Forms (BL Forms Treated by D-Clotterin) of Chlamydia muridarum on Screw Protection to vaginal infection with C. muridarum and the development of tubal pathology.

4 groups of 10 female mice were immunized by intraperitoneal injection on D0, J0 + 10, JO + 21 with either an extract of C57 / BL6 mouse embryonic fibroblasts (Mefs) or with the b-Lac (b-Lac) form. either with the Lac form diluted to one third of the usual dose (b-Lac / 3), or with the form De (De). These vaccine forms were produced in Mefs.

At day 32, the animals were cycled by subcutaneous injection of 50 μl of Deprovera (50 mg / ml, Pfizer).

At day 39 animals were infected vaginally with 10 ⁷ IFU of Chlamydia muridarum. On D3, D6, D8, D10 and D13 post infection, vaginal smears were performed and the presence of Chlamydia muridarum was assessed by titration of the infectious capacity of Chlamydiae extracted from these smears (Figure 2).

At 8 weeks after infection, the rest of the animals (n = 6) were sacrificed, dissected uterine horns and macroscopic lesions (fluid cysts and translucent zones in the uterine horns or oviduct) were examined using a binocular magnifying glass. . Only mice in the b-Lac group have no macroscopic lesions. The uterine horns were fixed with paraformaldehyde, dehydrated and paraffin embedded. Longitudinal sections were stained with HPS (Hemalum Phloxine, Saffron) to highlight the different structures of the uterine horn (myometrium and endometrium including epithelium and lamina propria). We evaluated the severity of microscopic involvement by the cell loss observed at the uterine lamina propria (Figure 3).

More animals with minor tubal lesions (grade 1) or no lesions (grade 0) were observed in the b-Lac and De groups, compared to the Mefs and b-Lac / 3 groups. The most severe lesions visible in the Mefs group are absent from the b-Lac, b-Lac / 3 and De groups.

These results thus confirm the protective effect of 3 intraperitoneal injections of b-Lac forms (with a confirmed dose effect) and of De forms, with respect to the vaginal infection by a virulent form of Chlamydia muridarum. This protection results in a decrease in the bacterial load from the beginning of the local infection, a specific antibody response detectable in the spleen of infected immunized mice, and protection against inflammatory genital lesions post infection in these same mice. Example 4: Study of lymphocytic activation after complete immunization followed or not by an infection.

1. Activation profile of T lymphocytes after complete immunization by the b-Lac and De vaccine forms in vivo

One week after complete immunization (three immunizations at one week interval each), splenocytes from individual mice were recovered as previously described and the activation profile of CD4 ⁺ T cells and CD8 ⁺ was studied by flow cytometry focusing on the expression of classical activation markers CD25, CD62L, CD44 and ICOS. The selection strategy (gating) of CD4 ⁺ T or CD8 ⁺ T lymphocyte populations used was as follows: FSC / SSC (diffraction of light emitted at small angles and at 90 °), Singulets (elimination of cell doublets), CD19 negative (exclusion of B lymphocytes), CD3 ⁺ (selection of T cells carrying a TCR) and CD4 ⁺ (CD4 ⁺ T lymphocytes) or CD8 ⁺ (CD8 ⁺ T lymphocytes). The study of the number of CD4 ⁺ regulatory T cells (Treg) was performed after permeabilization of splenocytes and intracellular labeling of the FoxP3 molecule. The gating strategy of the regulatory CD4 ⁺ T cells (Treg) used was FSC / SSC, Singulets, CD19 negative (B-cell exclusion), Fixable Viability Dye ⁺ (viable cell selection), CD3 ⁺ (T-lymphocytes). ), CD4 ⁺ (CD4 ⁺ T cells) and FoxP3 ⁺ (Treg selection, a strong expression of FoxP3 is a specific marker for Tregs). Statistical analyzes were performed using the GraphPad Prism software.

In the spleen, the total numbers of lymphocytes, or CD4 + or CD8 + T cells are not significantly different between the different groups (Figures 4, 5A, 6A). However, the number of activated CD4 ⁺ CD44 ^hi CD62L ^10W T ^cells is significantly increased following immunization with the b-Lac vaccine form only (Figure 35). The ICOS expression profile on CD4 ⁺ T cells also shows a very significant increase in the number of CD4 ⁺ ICOS ⁺ T cells (ICOS being a marker reflecting the inflammatory potential of CD4 ⁺ T cells) (Figure 5). In parallel, the FoxP3 intracellular labeling shows a decrease in the CD4 ⁺ regulatory lymphocyte population, significant in terms of numbers following immunization with the vaccine form De. The same trend is observed in the b-Lac group (FIG. 5E). The vaccine forms do not induce significant differences in CD8 ⁺ ICOS ⁺ T populations (Figure 6B). There is a significant increase in the number of CD8 ⁺ CD44 ⁺ CD44 ^hl CD62L ^10W T ^lymphocytes after immunization with the b-Lac form (Figure 6C). 2. Activation profile of T lymphocytes after complete immunization by the b-Lac and De vaccine forms followed by intravaginal infection with 10 ⁷ IFU of Chlamydia muridarum.

After complete immunization (three immunizations at one week interval each), the mice were cycled by an injection of progesterone (Deprovera, 50 μΙ per mouse) and infected with Chlamydia muridarum intravaginally at 10 ⁷ IFU. After one week post-infection, the mice were sacrificed and tested individually. Splenocytes and ganglia draining the genital tract (inguinal / para-aortic / mesenteric) were recovered and isolated. The activation profile and the number of CD4 ⁺ and CD8 ⁺ T lymphocytes were studied by flow cytometry as indicated in the previous paragraph (part 1) by focusing on the expression of CD25, CD62L, CD44 and ICOS. The study of the proliferation of T lymphocytes as well as the number of Tregs is carried out after permeabilization and intracellular labeling of the molecule Ki67 (proliferation) and FoxP3 (Treg). Statistical analyzes were performed using the GraphPad Prism software.

Figure 7 shows the total number of lymphoid cells of the lymph nodes draining the genital tract and spleen from the 4 PBS, MEF, b-Lac or De groups. It is very clear that immunization with the b-Lac form followed intravaginal mice resulted in a marked increase in the number of draining lymphocytes (p <0.05) and a marked decrease in the spleen (p <0.01).

In the spleen of these mice, a significant decrease in CD4 + CD25 + T cells (Figure 8B) and a comparable trend for CD4 + and CD4 + CD44 ^hi CD62L ^10W T ^cells (Figure 8A and 8C) are also observed for the b-Lac group. respectively) For CD8 + T cells, in the b-Lac group, they are significantly decreased (p <0.05, Figure 8D), as well as CD8 + CD25 + T (p <0.01, Figure 8E).

A mirror image is observed in the draining lymph nodes, with a significant increase of the same populations T CD4 + and CD4 + CD25 + (Fig.9A and C) in the b-Lac group, and a similar trend for the CD4 + T cells and CD4 + CD44 ^hi CD62L ^10W and ICOS ^hi CD4 ⁺ (Figure ^9B and D). The same observation applies CD8 + T cells, and CD8 + CD44 CD62L also significantly increased only in the b-Lac group (Figure 9 E and F).

In agreement with the results above, if we examine the numbers of proliferating CD4 + and CD8 + T lymphocytes (carriers of the Ki67 nuclear marker), there is a clear tendency to decrease in the spleen and increase in the lymph nodes. , still only in the b-Lac group (Figure 10).

The analyzes of the number of regulatory T lymphocytes (CD4 and FoxP3 marker carriers) lead to the same conclusions, still in the b-Lac group: tendency to decrease CD4 + KI67 + Treg in the spleen, and significant increases (p <0.05). ) CD4 + and CD4 + KI67 + T reg in draining lymph nodes (Figure 1 1).

All of these results suggest that immunizing injections of b-Lac forms induce Chlamydia muridarum specific activation and immune response in the spleen, with production of specific antibodies. In response to an intravaginal infection, activated T cells leave the spleen for the ganglia draining the genital tract. Thus an immune base causing the local bacterial load drop (effector lymphocytes) and the decrease of the local inflammatory reaction generating tissue lesions (regulatory T cells) is provided.

Claims

1. A vaccine composition comprising bacteria of the family Chlamydiaceae previously treated with at least one peptidoglycan inhibitor, or extracts of said treated bacteria for use in the treatment and / or prevention of infections with a bacterium of the family Chlamydiaceae.

2. Vaccine composition for treating and / or preventing pathologies caused by infection with a bacterium of the family Chlamydiaceae, said composition comprising bacteria of the family Chlamydiaceae previously treated with at least one peptidoglycan inhibitor or extracts of said bacteria treated .

3. The vaccine composition of any one of claims 1 or 2, characterized in that said extracts of bacteria of the family Chlamydiaceae previously treated with at least one peptidoglycan inhibitor are membrane extracts or cytoplasmic extracts.

4. The vaccine composition of any one of the preceding claims, characterized in that said inhibitor of petidoglycan is a β-lactam or D-cycloserine.

5. The vaccine composition of any one of the preceding claims, characterized in that said β-lactam is selected from the group consisting of amoxicillin, benzylpenicillin (penicillin G), phenoxymethylpenicillin (penicillin V), cloxacillin, cephadroxil, cefixime, imipenem, cefixime in combination with imipenem, mecillinam, clavulanic acid, tazobactam and sulbactam.

6. The vaccine composition of claim 5, characterized in that said 6-lactamine is penicillin G.

7. The vaccine composition of any one of the preceding claims, characterized in that said bacterium of the family Chlamydiaceae is Chlamydia trachomatis or Chlamydia muridarum.

8. The vaccine composition of any one of claims 2 to 7, characterized in that the pathology is an ocular pathology, a pathology genital, respiratory pathology, cardiovascular dysfunction, circulatory dysfunction, joint pathology or inflammatory disease.

9. The vaccine composition of claim 8 characterized in that the genital pathology is selected from the group consisting of lymphogranuloma venereum, urethritis, orchi-epididymitis, cervico-vaginitis, cervicitis, endocervites, endometritis, peri hepatitis and salpingitis.

10. Vaccine composition comprising bacteria of the family Chlamydiaceae previously treated with at least one peptidoglycan inhibitor or extracts of said bacteria, and an adjuvant.

1 1. A process for preparing the vaccine composition of claim 10, said method comprising a step of treating said bacteria of the family Chlamydiaceae with a peptidoglycan inhibitor.

The method of claim 11 comprising a prior step of infection of a host cell with said bacteria of the family Chlamydiaceae prior to the treatment step with a peptidoglycan inhibitor.

A method for detecting a bacterium of the Chlamydiaceae family in a sample from a subject suspected of being infected by said bacterium, comprising the steps of: a) contacting said sample with antibodies specific for said bacterium generated against said bacterium; bacterium previously treated with a peptidoglycan inhibitor, said antibodies comprising a label producing a detectable signal, or being attached to a detectably labeled reagent; b) allowing the bacterium present in said sample to bind to form antigen / antibody complexes; and c) determining the presence of said bacterium in said sample by said detectable label.

14. A diagnostic kit for detecting infection with a bacterium of the Chlamydiaceae family, comprising said bacterium previously treated with a peptidoglycan inhibitor together with substances for performing a humoral immunity determination assay against said bacterium, in a unit packing container.

15. Use of a bacterium of the family Chlamydiaceae previously treated with a peptidoglycan inhibitor as an in vitro diagnostic reagent in a binding assay, optionally in a diagnostic kit, for the detection of neutralizing antibodies conferring immunity against said bacterium.

16. Use of specific antibodies of a bacterium of the family Chlamydiaceae generated against said bacteria previously treated with a 6-lactam as in vitro diagnostic reagent in a binding assay, optionally in a diagnostic kit, for the detection of said bacterium.