WO2000054789A1 - Fractions membranaires bacteriennes a effet adjuvant - Google Patents
Fractions membranaires bacteriennes a effet adjuvant Download PDFInfo
- Publication number
- WO2000054789A1 WO2000054789A1 PCT/FR2000/000622 FR0000622W WO0054789A1 WO 2000054789 A1 WO2000054789 A1 WO 2000054789A1 FR 0000622 W FR0000622 W FR 0000622W WO 0054789 A1 WO0054789 A1 WO 0054789A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- use according
- antigen
- hapten
- membrane fraction
- membrane
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/12—Viral antigens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/12—Viral antigens
- A61K39/155—Paramyxoviridae, e.g. parainfluenza virus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/385—Haptens or antigens, bound to carriers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
- A61K2039/55511—Organic adjuvants
- A61K2039/55566—Emulsions, e.g. Freund's adjuvant, MF59
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
- A61K2039/55588—Adjuvants of undefined constitution
- A61K2039/55594—Adjuvants of undefined constitution from bacteria
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/57—Medicinal preparations containing antigens or antibodies characterised by the type of response, e.g. Th1, Th2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/60—Medicinal preparations containing antigens or antibodies characteristics by the carrier linked to the antigen
- A61K2039/6031—Proteins
- A61K2039/6068—Other bacterial proteins, e.g. OMP
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2760/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses negative-sense
- C12N2760/00011—Details
- C12N2760/16011—Orthomyxoviridae
- C12N2760/16111—Influenzavirus A, i.e. influenza A virus
- C12N2760/16134—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2760/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses negative-sense
- C12N2760/00011—Details
- C12N2760/18011—Paramyxoviridae
- C12N2760/18511—Pneumovirus, e.g. human respiratory syncytial virus
- C12N2760/18534—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
Definitions
- the present invention relates to the use of a membrane fraction of gram negative bacteria, in particular of Klebsiella pneumoniae, associated with an antigen or hapten for the preparation of a pharmaceutical composition intended to orient the immune response towards a Thl type response and / or of the mixed Thl / Th2 type directed against said antigen or hapten.
- the invention further comprises methods for preparing said membrane fractions and the pharmaceutical compositions containing them and their applications to the prevention and treatment of infectious diseases, in particular paramyxovirus infections such as RSV, and cancers, in particular those of which tumors are associated with tumor antigens.
- Vaccination is an effective way to prevent or reduce infections, in particular.
- the success of vaccination campaigns in this area has made it possible to extend the concept of vaccines to the fields of autoimmune diseases, cancer and fertility.
- vaccinating antigens are not always capable of inducing a rapid and sustained antibody response on their own, which requires the presence of adjuvants, that is to say of compounds which help them (from the Latin word adjuvare: to help) to induce such responses.
- the adjuvants constitute a group of various compounds as for their structure and their origin.
- water-in-oil emulsions incomplete Freund's adjuvant
- oil-in-water compounds of bacterial origin such as lipopolysaccharide derivatives of Gram negative bacteria, as well as salts aluminum.
- aluminum salts are used in humans as an adjuvant for vaccine preparations.
- Th lymphocytes Two types of Th lymphocytes can be distinguished according to the profile of cytokines produced: type 1 Th lymphocytes producing IFN- ⁇ and 1TL-2 and promoting the formation of IgG2a in mice, and type 2 Th lymphocytes producing 1TL-4, IL-5 and IL-10 with formation of IgGl in mice (Mosmann, TR and Sad S. Immunol. Today 1996, 17: 138).
- Thl / Th2 a mixed Thl / Th2 response for which the Thl response is close to or greater than Th2 response.
- the authors of the present invention have demonstrated specific properties of the membrane fraction of a gram-negative bacterium Klebsiella pneumoniae (called FMKp), in particular membrane fractions obtained by the methods as described below in the examples.
- FMKp membrane fraction associated with an antigen not only had the capacity to increase the antibody response directed against said antigen but also to redirect the cytokinic response towards a Th1 / Th2 profile, thus corresponding to the activity particular adjuvant sought, regardless of the mode of administration of said membrane fractions.
- the subject of the present invention is the use of a membrane fraction of gram-negative bacteria, in particular of Klebsiella pneumoniae, associated with an antigen or hapten to orient the immune response towards a Thl type and / or mixed type response.
- Thl / Th2 directed against said antigen or hapten, or for the preparation of a pharmaceutical composition intended to orient the immune response to a Thl and / or mixed Thl / Th2 type response directed against said antigen or hapten.
- Thl / Th2 in particular an orientation of the immune response is preferred which promotes the induction of a Thl response compared to the Thl / Th2 response obtained with the alum adjuvant.
- Thl / Th2 more particularly preferred is an orientation of the immune response which increases the titer of IgG2a antibodies directed against the associated antigen by a factor of at least 10, preferably at least 25, 50 and 100 relative to the titer in IgG2a obtained with the alum adjuvant.
- the immune response is oriented towards a Th1 and / or mixed Thl / Th2 type response in which the Th1 response is close to or greater than the Th2 response.
- neighbor is intended to denote a response which, expressed as the IgG2a antibody directed against the associated antigen, is at least equal to 0.5 times, preferably at least equal to 0.75 times, the titer in IgG1 antibody directed against said antigen, with a titer of IgG antibody directed against the associated antigen neighboring or greater than the titer of IgG antibody directed against the associated antigen obtained with the adjuvant alum or Freund.
- the invention also relates to the use according to the invention, characterized in that the membrane fraction comprises at least membrane fractions of two different strains of bacteria.
- bacterial membrane fraction is intended to denote in the present invention any purified or partially purified membrane fraction or extract obtained from a culture of said bacteria and the preparation process of which comprises at least one step of lysis of the bacteria obtained after culture. and a step of separating the fraction containing the membranes of said bacteria from the total lysate obtained after the lysis step, in particular by centrifugation or filtration.
- membrane fraction of bacteria when said bacterium is Klebsiella pneumoniae is also meant in the present invention protein P40, active fraction of the membrane fraction of Klebsiella pneumoniae, of amino acid sequence SEQ ID No. 2, or one of its fragments.
- the membrane fractions can be prepared according to methods known to those skilled in the art such as for example the method described by by Haeuw J.F. et al. (Eur. J. Biochem, 255, 446-454, 1998).
- the invention relates to a use according to the invention, characterized in that the membrane fraction is prepared by a process comprising the following stages: a) the culture of said bacteria in a culture medium allowing their growth followed by centrifugation of said culture; b) if necessary, deactivation of the lyric enzymes from the pellet of bacteria obtained in step a), then centrifugation of the suspension obtained; c) extraction and elimination of non-membrane proteins and nucleic acids from the pellet obtained in step a) or b) by at least one washing cycle of the pellet in an extraction solution; d) digestion of the membrane pellet obtained in step c) in the presence of proteolytic enzymes followed by centrifugation; e) at least one washing cycle of the pellet obtained in step d) in a physiological solution and / or in distilled water; and f) ultrasonication of the pellet obtained in step e).
- Step b) of deactivation of the lytic enzymes from the pellet of bacteria obtained in step a) can be carried out by any known methods of deactivation of enzymes, such as in particular by heating the bacterial pellet resuspended at a temperature preferably close to 100 ° C., or by addition of inhibitor of the activity of these enzymes.
- Step c) of extraction and elimination of the non-membrane proteins and of the nucleic acids from the pellet obtained in step a) or b) can be carried out for example by at least one washing cycle of the pellet in a solution d extraction corresponding to the addition of a hypertonic solution (extraction solution), preferably a saline solution of molarity close to 1 M, followed after a contact time sufficient for the desired effect of a centrifugation of the suspension obtained and the elimination of supernatant obtained after said centrifugation, this washing cycle can be repeated several times.
- a hypertonic solution extraction solution
- this washing cycle can be repeated several times.
- Step d) of digestion of the membrane pellet obtained in step c) can be carried out in the presence of a solution of proteolytic enzymes such as for example trypsin, chymotrypsin or any enzyme with known proteolytic activity, the conditions of the reaction, pH of the solution, temperature and duration of the reaction, preferably being adjusted to optimal conditions for the activity of the chosen enzyme (s), followed by centrifugation, this digestion cycle being able to be reproduced several times with the same enzyme, the same combination of enzymes or with a different enzyme for each digestion cycle performed.
- proteolytic enzymes such as for example trypsin, chymotrypsin or any enzyme with known proteolytic activity
- Step e) of washing the pellet obtained in step d) is carried out by taking up the pellet in a physiological solution or in distilled water followed, after sufficient contact time, by centrifugation, this cycle of washing can be repeated several times.
- step f) of ultrasonication of the pellet has the objective in particular of disintegrating and homogenizing the membrane fraction obtained at the end of step e).
- the ultrasonication conditions (duration and power) will be determined by a person skilled in the art depending for example on the amount of membrane fraction to be treated.
- the invention relates to a use according to the invention, characterized in that the membrane fraction is prepared by a process comprising the following steps: a) the culture of said bacteria in a culture medium allowing their growth followed, where appropriate, by centrifugation; b) freezing the culture medium or the pellet obtained in step a) followed by thawing and drying of the cells; c) elimination, by means of a DNase, of the nucleic acids from the dry cells obtained in step b) resuspended; d) grinding the cells obtained in step c) and clarifying the suspension obtained; e) precipitation in an acid medium of the suspension obtained in step d) and elimination of the pellet; f) neutralization of the supernatant obtained in step e) containing the membrane suspension, followed by dialysis and concentration of the membrane suspension; and g) sterilization of the concentrated membrane suspension obtained in step f).
- the thawing conditions in step b) of the process below will of course be determined by those skilled in the art depending on the amount
- step c) the removal of the nucleic acids is carried out for example by the addition of a DNase, at a final concentration of 5 mg / ml of a suspension of cells at a concentration equivalent to 5% dry cells.
- the grinding of the cells obtained in step c) can be carried out using any system or apparatus known to those skilled in the art for grinding cells such as presses or preferably such as grinding in a Manton loop Gaulinet for 30 minutes.
- the clarification of the suspension obtained after grinding can be carried out using any system or apparatus known to those skilled in the art for the clarification of bacterial cell shreds such as the Sharpless system.
- Stage e) of precipitation in acid medium of the suspension obtained in stage d) can be carried out for example with acetic acid.
- the precipitation is followed by the elimination of the pellet by means of a Sharpless type system and by the recovery of the supernatant.
- Step f) consists of a step in which the supernatant, obtained after precipitation in an acid medium, is neutralized, diluted, dialysed and then concentrated.
- the last step consists of a step of sterilizing the membrane fraction concentrate obtained in the previous step, for example by heating at 121 ° C for about 35 minutes.
- the invention relates in particular to the use according to the invention, characterized in that the membrane fraction is the P40 protein of Klebsiella pneumoniae of sequence SEQ ID No. 2, or one of its fragments.
- fragment of the P40 protein is intended to denote in particular any fragment of the amino acid sequence included in the amino acid sequence of the P40 protein capable of increasing a non-specific immune response and / or capable of inducing a response anti-tumor immune system, and comprising at least 5 amino acids, preferably at least 10 amino acids or more preferably at least 15 amino acids.
- said P40 protein, or its fragments can be obtained by chemical synthesis or in the form of recombinant peptides.
- the invention relates in particular to the use according to the invention, characterized in that said antigen or hapten is chosen from antigens or haptens specific for an infectious agent, such as a virus, a bacterium, a fungus or a parasite, or among antigens associated with tumor cells.
- an infectious agent such as a virus, a bacterium, a fungus or a parasite
- said antigens or haptens are preferably chosen from peptides, lipopeptides, polysaccharides, oligosaccharides, nucleic acids, lipids or any compound capable of specifically directing the immune response towards a Thl type response and / or of the mixed Thl / Th2 type against an antigen or hapten specific for an infectious agent or an antigen associated with a tumor cell.
- said antigen or hapten when it is of peptide nature can be obtained by chemical or recombinant synthesis.
- the invention further comprises the use according to the invention, characterized in that said antigen or hapten is coupled or mixed with said membrane fraction, in particular coupled by covalent bond with at least one of the compounds contained in the membrane fraction.
- the invention comprises the use according to the invention, characterized in that said antigen or hapten is covalently coupled to a support peptide to form a complex capable of specifically binding to mammalian serum albumin , preferably said support peptide is a peptide fragment derived from the G protein of the streptococcus, in particular the C-terminal fragment called BB.
- said complex can be prepared by genetic recombination.
- the chimeric or hybrid complex can be produced by recombinant DNA techniques by insertion or addition to a DNA sequence coding for said peptide fragment of the streptococcus protein G of a sequence coding for said antigen or hapten of a protein nature.
- the methods for synthesizing hybrid molecules include the methods used in genetic engineering to construct hybrid polynucleotides encoding the desired polypeptide sequences.
- the coupling by covalent bond can be achieved by chemical synthesis.
- one or more connecting elements may be introduced into at least one of the compounds contained in the membrane fraction and / or in said antigen or hapten to facilitate chemical coupling.
- the said linking element introduced is an amino acid.
- the covalent coupling between said compound of the membrane fraction and said antigen or hapten according to the invention can be carried out at the N- or C- terminal end of said compound of the membrane fraction or of said antigen or hapten, if these are by example of peptide nature.
- the bifunctional reagents allowing the coupling will be determined according to the end chosen to effect the coupling and to the nature of the said antigen or hapten to be coupled.
- the invention also includes the use according to the invention, characterized in that the coupling between said antigen, hapten or the complex and at least one of the compounds contained in the membrane fraction is carried out by genetic recombination when said antigen, hapten , or complex and said membrane compound are peptide in nature.
- the coupling between said antigen, hapten or complex, and at least one of the compounds contained in the membrane fraction can in fact be achieved by genetic recombination. It is possible, for example, before extracting its membrane fraction therefrom, beforehand transforming said gram-negative bacteria with a vector containing a nucleic construct coding for an antigen of interest or said complex, so that the bacterium thus transformed expresses antigen of interest or said complex attached to the membrane or anchored in the membrane of said bacteria.
- Such methods of expressing recombinant proteins attached to the membrane are well known and require, for example, the presence of a specific regulatory sequence such as a signal peptide type sequence.
- a subject of the invention is also the use according to the invention, characterized in that the pharmaceutical composition also comprises an agent making it possible to convey said membrane fraction associated with said antigen, hapten or complex in a form making it possible to improve its stability and / or its immunogenicity, such as in the form of an oil-in-water or water-in-oil emulsion, or in the form of a particle of liposome, microsphere, nanosphere type or any type of structure allowing the encapsulation and the presentation in particulate form of said membrane fraction associated with said antigen, hapten or complex.
- an agent making it possible to convey said membrane fraction associated with said antigen, hapten or complex in a form making it possible to improve its stability and / or its immunogenicity, such as in the form of an oil-in-water or water-in-oil emulsion, or in the form of a particle of liposome, microsphere, nanosphere type or any type of structure allowing the encapsulation and the presentation in particulate form of said membrane fraction associated
- the invention also relates to the use according to the invention, characterized in that said agent is chosen from aluminum salts, calcium salts, compounds of plant origin such as Quil A or saponin, or compounds of bacterial origin such as cholera, pertussis, tetanus toxoid or heat-labile toxin derivatives of E. coli.
- said agent is chosen from aluminum salts, calcium salts, compounds of plant origin such as Quil A or saponin, or compounds of bacterial origin such as cholera, pertussis, tetanus toxoid or heat-labile toxin derivatives of E. coli.
- the pharmaceutical composition further comprises an agent making it possible to regulate the immune response induced by said membrane fraction associated with said antigen, hapten or complex.
- an agent making it possible to regulate the immune response induced by said membrane fraction associated with said antigen, hapten or complex.
- regulatory agents preference is given in particular to cytokines, growth factors, hormones or cellular components such as nucleic acids, a protein of the family of heat shock proteins or ribosomes.
- a subject of the invention is also the use according to the invention, for the preparation of a pharmaceutical composition intended for the prevention or treatment of infectious diseases of viral, bacterial, fungal or parasitic origin, or for the prevention or treatment of cancers, in particular cancers whose tumors are associated with tumor antigens.
- infectious diseases of viral origin particular preference is given to infectious diseases caused by the paramyxoviruses, in particular by the parainfluenzae virus and more preferably by the respiratory syncytial virus (RSV).
- infectious diseases caused by the paramyxoviruses in particular by the parainfluenzae virus and more preferably by the respiratory syncytial virus (RSV).
- RSV respiratory syncytial virus
- the use according to the invention is characterized in that said antigen associated with the membrane fraction comprises the peptide G2Na, fragment of the protein G of the virus of amino acid sequence SEQ ID N ° 4, a peptide homologous to G2Na, the sequence of which has an identity rate of at least 80%, preferably 90%, 95% and 99%, after alignment with the sequence SEQ ID No. 4, or the peptide G2Na or the one of its counterparts, coupled by covalent bond to a C-terminal fragment (BB) of the streptococcal protein G to form a complex capable of binding to mammalian serum albumin, BB peptide as described in the documents Power et al.
- BB C-terminal fragment
- percentage, degree or level of identity between two nucleic acid or amino acid sequences within the meaning of the present invention is meant a percentage of identical nucleotides or amino acid residues between the two sequences to compare, obtained after the best alignment, this percentage being purely statistical and the differences between the two sequences being distributed randomly and over their entire length. Sequence comparisons between two nucleic acid or amino acid sequences are traditionally carried out by comparing these sequences after having optimally aligned them, said comparison being carried out by segment or by "comparison window" to identify and compare the regions. sequence similarity locale.
- the optimal alignment of the sequences for comparison can be achieved, besides manually, by means of the local homology algorithm of Smith and Waterman (1981) [Ad. App. Math. 2: 482], using the local homology algorithm of Neddleman and Wunsch (1970) [J. Mol. Biol. 48: 443], using the similarity search method of Pearson and Lipman (1988) [Proc. Natl. Acad. Sci. USA 85: 2444], using computer software using these algorithms (GAP, BESTFIT, FASTA and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, WI, or by BLAST comparison software N or BLAST P).
- the percentage of identity between two nucleic acid or amino acid sequences is determined by comparing these two optimally aligned sequences per comparison window in which the region of the nucleic acid or amino acid sequence to be compared. may include additions or deletions with respect to the reference sequence for optimal alignment between these two sequences.
- the percentage of identity is calculated by determining the number of identical positions for which the nucleotide or the amino acid residue is identical between the two sequences, by dividing this number of identical positions by the total number of positions in the comparison window. and multiplying the result obtained by 100 to obtain the percentage of identity between these two sequences.
- BLAST program "BLAST 2 sequences" available on the website http: // www. ncbi. nlm. nih.
- the invention relates to a process for the preparation of a membrane fraction of gram-negative bacteria, in particular Klebsiella pneumoniae, characterized in that it comprises the following steps: a) the culture of said bacteria in a medium culture allowing their growth followed by centrifugation of said culture; b) if necessary, deactivation of the lytic enzymes from the pellet of bacteria obtained in step a), then centrifugation of the suspension obtained; c) extraction and elimination of non-membrane proteins and nucleic acids from the pellet obtained in step a) or b) by at least one washing cycle of the pellet in an extraction solution; d) digestion of the membrane pellet obtained in step c) in the presence of protease enzymes followed by centrifugation; e) at least one washing cycle of the pellet obtained in step d) in a physiological solution and / or in distilled water; and f) ultrasonication of the pellet obtained in step e).
- the invention also includes the process for the preparation of a membrane fraction of gram negative bacteria, in particular Klebsiella pneumoniae, characterized in that it comprises the following stages: a) the culture of said bacteria in a culture medium allowing their continued growth where appropriate, centrifugation; b) freezing the culture medium or the pellet obtained in step a) followed by thawing and drying of the cells; c) elimination, by means of a DNase, of the nucleic acids from the dry cells obtained in step b) resuspended; d) grinding the cells obtained in step c) and clarifying the suspension obtained; e) precipitation in an acid medium of the suspension obtained in step d) and elimination of the pellet; f) neutralization of the supernatant obtained in step e) containing the membrane suspension, followed by dialysis and concentration of the membrane suspension; and g) sterilization of the concentrated membrane suspension obtained in step f).
- proteogly cane titer of the membrane fractions capable of being obtained by said methods active principle of FMKp, represented by the sum of the galactose and protein contents, is preferably understood:
- this titer will be: - for galactose: between 1.6 g / 1 and 2.6 g / 1;
- the invention further relates to the pharmaceutical compositions comprising a membrane fraction capable of being obtained by the methods according to the invention, preferably the said pharmaceutical compositions, further comprising an antigen, hapten or a complex, as defined above, associated to said membrane fraction, such as in particular the viral antigens or complexes specific to paramyxovirus, or the antigens associated with tumor cells.
- compositions according to the invention may also comprise agents such as vehicles, regulatory agents defined above.
- the pharmaceutical composition according to the invention is characterized in that said antigen associated with the membrane fraction comprises the peptide G2Na of sequence SEQ ID No. 4 of the respiratory syncytial virus, one of its counterparts as defined above , or said G2Na peptide, or one of its homologs, coupled by covalent bond to a C-terminal fragment (BB) of the Streptococcus G protein to form a complex capable of binding to mammalian serum albumin.
- BB C-terminal fragment
- FIG. 2 BBG2Na adjuvanted by FMKp -Titles IgGl and IgG2a anti-G2Na.
- Figure 3 BBG2Na adjuvanted by FMKp - Study of protection.
- Figure 4 Adjuvant effect of FMKp vis-à-vis Immugrip (influenza vaccine).
- the extraction of the membranes of K. pneumoniae 1145 from the centrifugation pellet of the step is preferably preceded by a step of destruction of the lytic enzymes of the cellular components contained in the pellet, for example by heating to 100 ° C. of that -this, possibly after re-solution.
- the actual extraction of the membranes from the centrifugation pellet is preferably carried out by treatment of the cellular components of the pellet, after a possible destruction of the lytic enzymes, using a saline solution, for example sodium chloride 1 M, one or more times, then centrifugation, preferably at 20,000 g, of the suspension obtained, the supernatant from this centrifugation, which is eliminated, contains the non-membrane impurities such as proteins and nucleic acids, while the pellet contains membranes.
- a saline solution for example sodium chloride 1 M
- the membranes are digested in the presence of proteolytic enzymes, preferably trypsin and chymotrypsin, in solution at pH 8 at 37 ° C for 4 hours. After digestion, the solution is homogenized by ultrasonication. The product thus obtained constitutes the membrane fraction called FMKp.
- proteolytic enzymes preferably trypsin and chymotrypsin
- This fraction is prepared from the pellet obtained by centrifugation at 40,000 g for 20 minutes. Said pellet is resuspended in physiological saline and this suspension is brought for 10 minutes to 100 ° C. in a boiling water bath to deactivate the lytic enzymes. After cooling, centrifugation is carried out for 30 min at 20,000 g. The pellet obtained is extracted twice with 1M NaCl to remove the proteins and the nucleic acids. The membranes are collected by centrifugation for 30 minutes at 20,000 g.
- a constant volume dialysis is then carried out on PUF 100 up to 800 ⁇ cm, followed by a concentration of the membrane suspension (SM) thus obtained, at 11 1 / kg of dry cells.
- the SM is then autoclaved at + 121 ° C for 35 min which can be stored at + 4 ° C for 6 weeks.
- Characteristics of FMKp By definition, the titer in cane proteogly, active principle of FMKp, is equal to the sum of the galactose and protein contents. - Galactose: on average 2.2 g 11.
- BBG2Na is a recombinant protein produced in E. coll. It consists of the peptide G2Na of sequence SEQ ID No. 4, the fragment of protein G of the Respiratory Syncytial Virus (RSV) type A ranging from residue 130 to residue 230, fused to BB, a fragment of the G protein of Streptococci , having the ability to bind to serum albumin.
- RSV Respiratory Syncytial Virus
- BBG2Na is an RSV vaccine (Power U. Virology 1997, 230: 155-166).
- BALB / c mice receive 2 injections subcutaneously of 20 ⁇ g of
- BBG2Na and different amounts of FMKp Blood samples are taken on D28 and the serum antibody titers are determined by ELISA with G2Na in solid phase. The results obtained are illustrated in FIG. 1. Surprisingly, they show that FMKp significantly increases the IgG anti-G2Na response; the anti-G2Na IgG titer achieved is similar to that induced by alum or Freund's adjuvant. The effect is dose-dependent: it is observed from 5 ⁇ g of FMKp, maximum from 50 ⁇ g of FMKp and remains stable with 100 ⁇ g of FMKp. FMKp is therefore a potential adjuvant for BBG2Na.
- FMKp makes it possible to redirect the antibody response without affecting the ability to protect mice against a challenge to VRS-A.
- Example 3 Adjuvant Effect of FMKp on an Inactivated Virus (Influenza Vaccine)
- BALB / c mice receive a single injection of 0.01 ⁇ g of Immugrip TM (influenza vaccine marketed by INAVA Laboratories), and different amounts of FMKp. The products are co-administered. The injection is made subcutaneously on D0. Blood samples are taken on D7, D14 and D21.
- the anti-Immugrip serum IgG antibody titer is by ELISA with Immugrip at 2 ⁇ g / ml in solid phase. The results presented (FIG.
- FMKp significantly increases the anti-Immugrip antibody titer and this from the lowest dose of FMKp, namely 0.1 ⁇ g.
- the adjuvant effect is dose-dependent. It is interesting to note that the presence of FMKp induces the generation of an earlier antibody response, observed from D7, compared to the non-adjuvanted Immugrip control. This effect is not obtained with the reference adjuvant, the complete Freund's adjuvant (CFA).
- CFA complete Freund's adjuvant
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pulmonology (AREA)
- Molecular Biology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicinal Preparation (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE60032119T DE60032119T2 (de) | 1999-03-15 | 2000-03-15 | Bakterienwandfraktionen mit adjuvansaktivität |
BR0009051-4A BR0009051A (pt) | 1999-03-15 | 2000-03-15 | Utilização de uma fração de membrana de klebsiella pneumoniae associada a um antìgeno ou hapteno, e, composição farmacêutica |
AU32980/00A AU778957B2 (en) | 1999-03-15 | 2000-03-15 | Bacterial membrane fractions with adjuvant effect |
EP00910946A EP1158993B1 (fr) | 1999-03-15 | 2000-03-15 | Fractions membranaires bacteriennes a effet adjuvant |
JP2000604864A JP2002539169A (ja) | 1999-03-15 | 2000-03-15 | アジュバント効果を有する細菌膜分画 |
CA002367917A CA2367917A1 (fr) | 1999-03-15 | 2000-03-15 | Fractions membranaires bacteriennes a effet adjuvant |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9903153A FR2790959B1 (fr) | 1999-03-15 | 1999-03-15 | Utilisation de fractions membranaires bacteriennes a effet adjuvant, leurs procedes de preparation et composition pharmaceutique les contenant |
FR99/03153 | 1999-03-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000054789A1 true WO2000054789A1 (fr) | 2000-09-21 |
Family
ID=9543184
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2000/000622 WO2000054789A1 (fr) | 1999-03-15 | 2000-03-15 | Fractions membranaires bacteriennes a effet adjuvant |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP1158993B1 (fr) |
JP (1) | JP2002539169A (fr) |
CN (1) | CN1151799C (fr) |
AT (1) | ATE346602T1 (fr) |
AU (1) | AU778957B2 (fr) |
BR (1) | BR0009051A (fr) |
CA (1) | CA2367917A1 (fr) |
DE (1) | DE60032119T2 (fr) |
ES (1) | ES2276673T3 (fr) |
FR (1) | FR2790959B1 (fr) |
WO (1) | WO2000054789A1 (fr) |
ZA (1) | ZA200107628B (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002074939A1 (fr) * | 2001-03-15 | 2002-09-26 | Pierre Fabre Medicament | Utilisation d'une fraction membranaire de bacteries a gram negatif pour induire la maturation des cellules dendritiques |
US9255140B2 (en) | 2004-06-15 | 2016-02-09 | New York Blood Center, Inc. | Adjuvancy and immune potentiating properties of natural products of Onchocerca volvulus |
US9624238B2 (en) | 2011-05-27 | 2017-04-18 | Lexicon Pharmaceuticals, Inc. | 4H-thieno[3,2-C]chromene-based inhibitors of Notum Pectinacetylesterase and methods of their use |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2596064A1 (fr) * | 1986-03-18 | 1987-09-25 | Pf Medicament | Procedes industriels de fabrication de vaccins ribosomaux et vaccins ribosomaux obtenus |
FR2718452A1 (fr) * | 1994-04-06 | 1995-10-13 | Pf Medicament | Elément d'immunogène, agent immunogène, composition pharmaceutique et procédé de préparation. |
FR2726472A1 (fr) * | 1994-11-07 | 1996-05-10 | Pf Medicament | Proteine porteuse a effet adjuvant, complexe immunogene la contenant, leur procede de preparation, sequence nucleotidique et vaccin |
FR2748476A1 (fr) * | 1996-05-07 | 1997-11-14 | Pf Medicament | Complexe immunogene, son utilisation, son procede de preparation et vaccin le contenant |
FR2766192A1 (fr) * | 1997-07-17 | 1999-01-22 | Pf Medicament | Epitopes du vrs et anticorps les comportant, utiles dans le diagnostic et la therapie |
WO2000027432A1 (fr) * | 1998-11-06 | 2000-05-18 | Pierre Fabre Medicament | UTILISATION D'UNE PROTEINE OmpA D'ENTEROBACTERIE, POUR LE CIBLAGE SPECIFIQUE VERS LES CELLULES PRESENTATRICES D'ANTIGENES |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1331355C (fr) * | 1986-04-21 | 1994-08-09 | Bioenterprises Pty. Ltd | Immunopotentialisation |
WO1999004010A1 (fr) * | 1997-07-18 | 1999-01-28 | Connaught Laboratories Limited | Vaccins d'acide nucleique codant une proteine g du virus respiratoire syncytial |
-
1999
- 1999-03-15 FR FR9903153A patent/FR2790959B1/fr not_active Expired - Fee Related
-
2000
- 2000-03-15 AU AU32980/00A patent/AU778957B2/en not_active Ceased
- 2000-03-15 CA CA002367917A patent/CA2367917A1/fr not_active Abandoned
- 2000-03-15 WO PCT/FR2000/000622 patent/WO2000054789A1/fr active IP Right Grant
- 2000-03-15 AT AT00910946T patent/ATE346602T1/de not_active IP Right Cessation
- 2000-03-15 EP EP00910946A patent/EP1158993B1/fr not_active Expired - Lifetime
- 2000-03-15 CN CNB008050449A patent/CN1151799C/zh not_active Expired - Fee Related
- 2000-03-15 DE DE60032119T patent/DE60032119T2/de not_active Expired - Fee Related
- 2000-03-15 JP JP2000604864A patent/JP2002539169A/ja active Pending
- 2000-03-15 BR BR0009051-4A patent/BR0009051A/pt not_active Application Discontinuation
- 2000-03-15 ES ES00910946T patent/ES2276673T3/es not_active Expired - Lifetime
-
2001
- 2001-09-17 ZA ZA200107628A patent/ZA200107628B/en unknown
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2596064A1 (fr) * | 1986-03-18 | 1987-09-25 | Pf Medicament | Procedes industriels de fabrication de vaccins ribosomaux et vaccins ribosomaux obtenus |
FR2718452A1 (fr) * | 1994-04-06 | 1995-10-13 | Pf Medicament | Elément d'immunogène, agent immunogène, composition pharmaceutique et procédé de préparation. |
FR2726472A1 (fr) * | 1994-11-07 | 1996-05-10 | Pf Medicament | Proteine porteuse a effet adjuvant, complexe immunogene la contenant, leur procede de preparation, sequence nucleotidique et vaccin |
FR2748476A1 (fr) * | 1996-05-07 | 1997-11-14 | Pf Medicament | Complexe immunogene, son utilisation, son procede de preparation et vaccin le contenant |
FR2766192A1 (fr) * | 1997-07-17 | 1999-01-22 | Pf Medicament | Epitopes du vrs et anticorps les comportant, utiles dans le diagnostic et la therapie |
WO2000027432A1 (fr) * | 1998-11-06 | 2000-05-18 | Pierre Fabre Medicament | UTILISATION D'UNE PROTEINE OmpA D'ENTEROBACTERIE, POUR LE CIBLAGE SPECIFIQUE VERS LES CELLULES PRESENTATRICES D'ANTIGENES |
Non-Patent Citations (2)
Title |
---|
HAEUW J F ET AL: "The recombinant Klebsiella pneumoniae outer membrane protein OmpA has carrier properties for conjugated antigenic peptides", EUROPEAN JOURNAL OF BIOCHEMISTRY, vol. 255, no. 2, 15 July 1998 (1998-07-15), pages 446 - 454, XP002116544 * |
RAULY I ET AL.: "Carrier properties of a protein derived from outer membrane protein A of Klebsiella pneumoniae", INFECTION AND IMMUNITY, vol. 67, no. 11, November 1999 (1999-11-01), pages 5547 - 5551, XP002138526 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002074939A1 (fr) * | 2001-03-15 | 2002-09-26 | Pierre Fabre Medicament | Utilisation d'une fraction membranaire de bacteries a gram negatif pour induire la maturation des cellules dendritiques |
US9255140B2 (en) | 2004-06-15 | 2016-02-09 | New York Blood Center, Inc. | Adjuvancy and immune potentiating properties of natural products of Onchocerca volvulus |
US9624238B2 (en) | 2011-05-27 | 2017-04-18 | Lexicon Pharmaceuticals, Inc. | 4H-thieno[3,2-C]chromene-based inhibitors of Notum Pectinacetylesterase and methods of their use |
Also Published As
Publication number | Publication date |
---|---|
ES2276673T3 (es) | 2007-07-01 |
DE60032119T2 (de) | 2007-09-27 |
EP1158993B1 (fr) | 2006-11-29 |
FR2790959A1 (fr) | 2000-09-22 |
ZA200107628B (en) | 2002-07-22 |
CA2367917A1 (fr) | 2000-09-21 |
BR0009051A (pt) | 2002-01-02 |
DE60032119D1 (de) | 2007-01-11 |
CN1343124A (zh) | 2002-04-03 |
JP2002539169A (ja) | 2002-11-19 |
AU778957B2 (en) | 2004-12-23 |
ATE346602T1 (de) | 2006-12-15 |
EP1158993A1 (fr) | 2001-12-05 |
FR2790959B1 (fr) | 2003-06-27 |
CN1151799C (zh) | 2004-06-02 |
AU3298000A (en) | 2000-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5327873B2 (ja) | リコンビナントヘリコバクターピロリの経口ワクチン及びその調製方法 | |
JP2011190278A (ja) | 粘膜体表面に接触させてワクチン抗原を包含する物質の効果を調節する新規非抗原性粘膜アジュバント処方 | |
FR2732605A1 (fr) | Composition destinee a l'induction d'une reponse immunitaire mucosale | |
EP0791063B1 (fr) | Proteine porteuse a effet adjuvant, complexe immunogene la contenant, leur procede de preparation, sequence nucleotidique et vaccin | |
EP0089266B2 (fr) | Procédé de préparation de protéoglycanes immunostimulants inducteurs d'interféron, protéoglycanes obtenus et médicament les contenant | |
US8048434B2 (en) | Vaccine adjuvants | |
EP1124577B1 (fr) | Utilisation d'une proteine ompa d'enterobacterie, pour le ciblage specifique vers les cellules presentatrices d'antigenes | |
US9119803B2 (en) | Carious tooth vaccine and preparation method | |
EP1158993B1 (fr) | Fractions membranaires bacteriennes a effet adjuvant | |
JP2007509166A (ja) | 生得的免疫およびアレルギー性免疫を活性化させるための組成物および方法 | |
CA2367211A1 (fr) | Fractions membranaires bacteriennes immunostimulantes dans le traitement de cancers | |
EP1292333A1 (fr) | Composition adjuvante comprenant la proteine fha ou un fragment de la proteine fha sous forme libre | |
EP1244690B1 (fr) | Procede de preparation d'un polypeptide soluble en solvant aqueux en absence de detergent | |
MXPA01009346A (en) | Bacterial membrane fractions with adjuvant effect | |
WO1992000096A1 (fr) | Composition vaccinale destinee au traitement d'affections humaines a chlamydiae | |
WO2001082959A1 (fr) | Proteine omp associee a un lysat de cellules tumorales autologues et/ou heterologues | |
FR2808194A1 (fr) | Utilisation de particules hydrophiles portant ou non des ligands ioniques pour ameliorer les proprietes immunomodulatrices d'une substance autre qu'un antigene, et les compositions pharmaceutiques ainsi obtenues | |
WO2001087326A1 (fr) | UTILISATION D'UNE PROTEINE OmpA D'ENTEROBACTERIE COMME AGENT ANTIMICROBIEN | |
MXPA97001445A (en) | Effective mutating enterotoxin as adjuvant oral no tox |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 00805044.9 Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AU BR CA CN JP MX US ZA |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 32980/00 Country of ref document: AU |
|
ENP | Entry into the national phase |
Ref document number: 2367917 Country of ref document: CA Ref document number: 2367917 Country of ref document: CA Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 09936676 Country of ref document: US Ref document number: PA/a/2001/009346 Country of ref document: MX |
|
ENP | Entry into the national phase |
Ref document number: 2000 604864 Country of ref document: JP Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2001/07628 Country of ref document: ZA Ref document number: 200107628 Country of ref document: ZA |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2000910946 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 2000910946 Country of ref document: EP |
|
WWG | Wipo information: grant in national office |
Ref document number: 32980/00 Country of ref document: AU |
|
WWG | Wipo information: grant in national office |
Ref document number: 2000910946 Country of ref document: EP |