US20060159697A1 - Modified bordetella adenylate cyclase comprising or lacking CD11b/CD18 interaction domain and uses thereof - Google Patents

Modified bordetella adenylate cyclase comprising or lacking CD11b/CD18 interaction domain and uses thereof Download PDF

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US20060159697A1
US20060159697A1 US11/304,590 US30459005A US2006159697A1 US 20060159697 A1 US20060159697 A1 US 20060159697A1 US 30459005 A US30459005 A US 30459005A US 2006159697 A1 US2006159697 A1 US 2006159697A1
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cd11b
adenylate cyclase
cyaa
bordetella
cells
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Claude Leclerc
Mohammed El-Idrissi
Daniel Ladant
Cecile Bauche
Peter Sebo
Jirina Loucka
Radim Osicka
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Centre National de la Recherche Scientifique CNRS
Institut Pasteur de Lille
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Assigned to CENTRE NATIONAL DE LA RECHERCHE SCIENTIQUE, INSTITUT PASTEUR reassignment CENTRE NATIONAL DE LA RECHERCHE SCIENTIQUE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: EL-AZAMI EL-IDRISSI, MOHAMMED, LADANT, DANIEL, LOUCKA, JIRINA, OSICKA, RADIM, SEBO, PETER, BAUCHE, CECILE, LECLERC, CLAUDE
Publication of US20060159697A1 publication Critical patent/US20060159697A1/en
Priority to US11/713,708 priority Critical patent/US7906123B1/en
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/235—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Bordetella (G)
    • 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
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/88—Lyases (4.)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • 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
    • 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
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/52—Genes encoding for enzymes or proenzymes
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y406/00—Phosphorus-oxygen lyases (4.6)
    • C12Y406/01—Phosphorus-oxygen lyases (4.6.1)
    • C12Y406/01001—Aodenylate cyclase (4.6.1.1)
    • 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
    • A61K39/02—Bacterial antigens
    • A61K2039/10—Brucella; Bordetella, e.g. Bordetella pertussis; Not used, see subgroups
    • 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
    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A61K2039/53—DNA (RNA) vaccination
    • 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

Definitions

  • the invention relates to modified Bordetella adenylate cyclase toxins which are deficient for CD11b/CD18 binding and to their use in the preparation of pharmaceutical composition for the treatment of whooping cough and/or for the protection against Bordetella infection.
  • the invention also relates to specific fragments of Bordetella adenylate cyclase comprising the CD11b/CD18 interaction domain and to their use, especially for targeting a molecule of interest to CD11b expressing cells.
  • Bordetella comprises four species, i.e., Bordetella pertussis, Bordetella parapertussis, Bordetella bronchiseptica and Bordetella avium.
  • Bordetellae are Gram-negative coccobacilli responsible for respiratory infections. Bordetella pertussis and Bordetella parapertussis are strictly human pathogens. Bordetella bronchiseptica is pathogenic for various mammals, and more rarely for man, and, in distinction to B. pertussis and B. parapertussis , is capable of surviving outside the host. Bordetella avium is pathogenic for birds.
  • B. pertussis which is the etiologic agent of whooping cough, a highly contagious childhood respiratory disease, characterized by bronchopneumonia and paroxysmal coughing interrupted by inspiratory whoops.
  • European patent EP 0 424 158 (Institut Pasteur) recites the use of Bordetella adenylate cyclase as protective antigens against both Bordetella pertussis and Bordetella bronchiseptica.
  • European patent EP 0 338 169 (Institut Pasteur) also describes the use of active adenylate cyclase preparations from Bordetella parapertussis as protective antigens against whooping cough.
  • the adenylate cyclase (also referred hereafter by the term CyaA) is a crucial factor in the virulence strategy of the bacteria during the early phases of respiratory tract colonization (Goodwin and Weiss, 1990; Khelef et al., 1992).
  • the toxin allows the pathogen to escape host immune surveillance, mainly, by intoxicating neutrophils and macrophages causing phagocyte impotence and inducing macrophage apoptosis (Confer and Eaton, 1982; Gueirard et al., 1998; Harvill et al., 1999; Khelef and Guiso, 1995; Khelef et al., 1993).
  • CyaA was shown to induce protective immunity against B. pertussis lung colonization in a mouse model (Betsou et al., 1993; Betsou et al., 1995; Hormozi et al., 1999).
  • CyaA is a 1706 aminoacid residue-long polypetide consisting of four functional domains; the adenylate cyclase activity (AC) domain (residues 1 to 400), the hydrophobic channel-forming domain (residues 500 to 700), the calcium-binding glycin/aspartate rich repeat domain (residues 1000 to 1600), and the C-terminal domain harboring a secretion signal (residues 1600 to 1706).
  • AC adenylate cyclase activity
  • AC adenylate cyclase activity domain
  • hydrophobic channel-forming domain residues 500 to 700
  • the calcium-binding glycin/aspartate rich repeat domain (residues 1000 to 1600)
  • the C-terminal domain harboring a secretion signal (residues 1600 to 1706).
  • CyaA is able to invade eukaryotic cells and translocate its catalytic domain into the cytoplasm where, upon activation by endogenous calmodulin, it catalyzes the conversion of ATP into cAMP (Ladant and Ullmann, 1999).
  • the accumulation of cAMP in the cell cytosol is considered to be responsible for the toxic effect of this toxin (Rogel et al., 1991).
  • the main consequences of this intoxication are cell apoptosis and the alteration of phagocytic abilities and superoxide production (Confer and Eaton, 1982; Friedman et al., 1987; Khelef et al., 1993; Njamkepo et al., 2000; Pearson et al., 1987).
  • CyaA requires calcium to acquire a translocation-specific conformation that allows the delivery of the catalytic domain into the cell cytosol (Rogel and Hanski, 1992; Rose et al., 1995).
  • CyaA is produced as an inactive protoxin, proCyaA, which after post-translational modification by an acyltransferase, the product of the cyaC gene, becomes an active toxin.
  • This covalent post-translational fatty-acylation is required for translocation of the toxin through target cell membranes and the delivery of its catalytic AC domain as well as for the formation of hemolytic cation-selective channels.
  • CyaA can penetrate a wide range of cell types, including the mammalian erythrocytes lacking membrane trafficking (Bellalou et al., 1990; Gray et al., 1999; Rogel and Hanski, 1992). In contrast, CyaA toxicity effects such as the abrogation of phagocytic capacity and the induction of apoptosis were mainly elucidated on immune cells, namely neutrophils and macrophages (Confer and Eaton, 1982; Khelef et al., 1993). In addition, in a mouse respiratory infection, CyaA was shown to display specific intoxication towards alveolar macrophages (Gueirard et al., 1998).
  • Vaccine comprising recombinant adenylate cyclase toxin produced by B. pertussis fixed to heterologous epitopes is also described in patent WO 93/21324 (Institut Pasteur, 1993). It has been recently demonstrated that CyaA binds specifically to target cells through the ⁇ M ⁇ 2 integrin (CD11b/CD18). This binding was saturable and completely inhibited by anti-CD11b monoclonal antibodies. CyaA displayed a selective cytotoxicity towards CD11b + cells showing that its interaction with CD11b is required for the translocation of the catalytic domain and the subsequent cAMP increase and cell death.
  • the CD11b protein is a member of the large family of ⁇ 2 integrins, the leukocyte adhesion molecules, which comprizes LFA1 (CD11a), MAC-1 (CD11b) and p150,95 (CD11c).
  • the members of this family differ by their ⁇ -chain which is expressed as an obligate heterodimer with a ⁇ chain (CD18) (Arnaout, 1990).
  • CD11b also known as complement type 3 receptor (CR3), is expressed on macrophages, neutrophils, dendritic cells, NK cells, peritoneal B-1 cells and a subset of CD8+ T cells (Arnaout, 1990; Bell et al., 1999).
  • CD11b binds various ligands, such as the intracellular adhesion molecule ICAM-1, fibrinogen, coagulant factor X and inactivated complement component C3b (iC3b) (Altieri and Edgington, 1988; Beller et al., 1982; Diamond et al., 1990; Wright et al., 1988).
  • EP1188446 (Institut Pasteur) describes proteinaceous vectors comprising recombinant Bordetella species adenylate cyclase for targeting a molecule of interest, and especially an antigen to dendritic cells.
  • the present invention is now based on the discovery that one or several regions of the Bordetella pertussis adenylate cyclase comprised within the amino acid sequence extending from amino acid 1166 to amino acid 1281 (SEQ ID NO:2) are critical for the interaction of the toxin with CD11b/CD18. This region, necessary to provide binding capacity of CyaA to CD11b/CD18 can further be combined with other regions of CyaA acting as accessory regions.
  • the invention also provides the use of the identified CD11b/CD18 interaction domain to generate neutralizing antibodies, capable of blocking the interaction of native adenylate cyclase produced by infectious bacteria with cell receptors.
  • the protein of the invention can be used, as the active principle, in a vaccine against whooping cough.
  • the mutation(s) within the CD11b/CD18 interaction domain thus preserves immune cells from potentially negative effects, such as signalling upon the integrin engagement by the toxoid and/or some functional interference due to competition for binding to CD11b with the CyaA toxoid, which also serves as the complement receptor CR3.
  • polypeptide refers to a single chain of amino acids linked by peptide bonds, comprising at least 6 amino acids, preferably at least 10 amino acids, and more preferably at least 50 amino acids.
  • protein refers to a macromolecule which essentially consists of one or more polypeptides.
  • Bordetella adenylate cyclase encompasses, within the present invention, the calmodulin-dependent adenylate cyclase which is naturally synthesized in Bordetella species, and which is a major virulence factor mandatory for the initial phases of bacterial colonization in the lung.
  • the protein of the invention is obtained by modification of the Bordetella pertussis adenylate cyclase, the agent of whooping cough in human.
  • the adenylate cyclase is synthesized and secreted in the form of a polypeptide of 1706 amino acids (SEQ ID NO:1):
  • the calmodulin-dependent catalytic activity is localized in the first 400 amino acids, this domain being hereafter referred to as “the N-terminal catalytic domain”.
  • said adenylate cyclase toxin is rendered invasive and hemolytic when post-translationally modified by the coexpression of the cyaC gene product.
  • CD11b/CD18 interaction domain refers either to
  • the CD11b/CD18 interaction domain of Bordetella bronchiseptica is represented by SEQ ID NO: 4.
  • the expression “deficient for CD11b/CD18 binding” means that the protein of the invention does not compete with the wild-type Bordetella adenylate cyclase for binding to CD11b/CD18 ⁇ m ⁇ 2 expressing cells.
  • the “CD11b/CD18 ⁇ m ⁇ 2 ” or “CD11b/CD18” refers to the cellular receptor of the Bordetella adenylate cyclase (Guermonprez et al., 2001). Examples of binding assays to evaluate specific binding of a recombinant toxin to CD11b/CD18 ⁇ m ⁇ 2 expressing cells are described in the following experimental part.
  • the protein of the invention preferably has less than 50% of binding affinity to CD11b/CD18 ⁇ m ⁇ 2 as compared to wild-type Bordetella adenylate cyclase. Most preferably, the protein of the invention has less than 10% and more preferably less than 5% of the assayed binding affinity.
  • CD11b expressing cells relates to the cells that express the CD11b/CD18 ⁇ m ⁇ 2 on their surface.
  • these cells are granulocytes/neutrophils, macrophages, NK cells, subsets of T CD8+ and B cells and myeloid dendritic cells.
  • the CD11b/CD18 interaction domain of a Bordetella adenylate cyclase is modified by insertion, deletion or substitution of one or more amino acid, the resulting protein being deficient for CD11b/CD18 binding.
  • the CD11b/CD18 interaction domain is modified by insertion of a peptide therein.
  • a sequence consisting of between 6 to 12 residues is inserted in the CD11b/CD18 interaction domain.
  • Specific embodiments include Bordetella pertussis adenylate cyclase modified by insertion between residues 1166 and 1167 or between residues 1281 and 1282 (the number indicates the position of the amino acids in the wild type Bordetella pertussis adenylate cyclase), of a peptide containing between 6 to 12 amino acids.
  • Examples of epitope insertions of the FLAG sequence at these positions are described in the following Experimental Part, hereafter referred to as CyaA1166/FLAG and CyaA1281/FLAG.
  • residues which are shown to be involved in the binding to CD11b/CD18 can be deleted or replaced by non-functional residues.
  • the Bordetella adenylate cyclase is modified by insertion, deletion or substitution of one or more amino acid in the region extending from residue 1208 to 1243 in Bordetella pertussis adenylate cyclase or in corresponding regions of other Bordetella adenylate cyclases.
  • Preferred embodiments of the protein of the invention include a Bordetella pertussis adenylate cyclase containing deletions of one or more of the amino acids or their replacement by non-functional amino acids.
  • the Bordetella adenylate cyclase is modified by the complete deletion of the CD11b/CD18 interaction domain.
  • the Bordetella pertussis adenylate cyclase is modified by deletion of the amino acids extending from position 1245 to position 1273, these amino acids being optionally replaced by non functional amino acids, for example an octapeptide as exemplified in the Experimental Part, hereafter referred to as the CyaA ⁇ 1245-1273.
  • the Bordetella adenylate cyclase is modified such that the catalytic activity is ablated.
  • the Bordetella adenylate cyclase is further modified by insertion, deletion or substitution of one or more amino acids in the N-terminal catalytic domain, wherein said modified Bordetella adenylate cyclase has a catalytic activity which is decreased as compared to the wild-type Bordetella adenylate cyclase catalytic activity.
  • the catalytic activity represents less than 10% of the catalytic activity of the wild-type Bordetella adenylate cyclase and is more preferably non significant.
  • mutants in the N-terminal catalytic domain are described in the Art (for example in WO 93/21324, Institut Pasteur).
  • Embodiments of the protein of the invention include modified Bordetella species adenylate cyclase lacking at least the amino acids 1 to 300 of the N-terminal catalytic domain and preferably lacking amino acids 1 to 373.
  • dipeptide insertions can be done into the ATP-binding site between residues 188 and 190 of adenylate cyclase of Bordetella pertussis , or the corresponding residues in adenylate cyclase from other Bordetella species.
  • acylation of the Bordetella adenylate cyclase is involved in CD11b/CD18 binding and subsequent translocation of the toxin into the cell. Accordingly, in one preferred embodiment of the protein of the invention, the protein is not acylated.
  • the Bordetella adenylate cyclase is further modified in the amino acids which are acylated post-translationally. These amino acids correspond to Lys-983 and Lys-860 of the Bordetella pertussis adenylate cyclase.
  • the protein is not acylated in position 983 and/or 860 of the adenylate cyclase sequence.
  • the protein of the invention is acylated.
  • the protein of the invention is preferably immunogenic, yet substantially non toxic protein, i.e. a protein that is at least deficient for cell receptor binding, and optionally in adenylate cyclase activity, but which is still specifically recognized by anti-adenylate cyclase toxin antibodies.
  • the invention also relates to the pharmaceutical composition comprising the protein defined above, in combination with a pharmaceutically acceptable vehicle.
  • said composition is a vaccine suitable for administration in a human or an animal.
  • the vaccine is preferably capable of inducing immunity against whooping cough.
  • Such vaccine comprises an immunoprotective and non-toxic amount of the protein of the invention.
  • Said composition may further comprise one or several suitable priming adjuvants accordingly.
  • Other antigens which are known to be desirably administered in conjugation with the protein of the invention may also be included in the vaccine of the invention.
  • additional components include other known protective antigen of Bordetella , tetanus toxoid and/or diphteria toxoid.
  • the invention further relates to a method for immunizing a human or an animal against Bordetella infection and/or symptoms associated to disease caused by Bordetella infection, which comprises administering the vaccine of the subject invention to such human or animal.
  • the route of administration of the vaccine of the invention may be any suitable route which delivers an immunoprotective amount of the protein of the invention to the host.
  • the vaccine is preferably administered parenterally via the intramuscular or subcutaneous routes.
  • Other routes of administration may also be employed, where desired, such as oral administration or via other parenteral routes, i.e., intradermally, intranasally or intravenously.
  • Another aspect of the present invention relates to the use of the protein of the invention, in the preparation of a medicament for the treatment, in human or in an animal, of disease symptoms associated with whooping cough and/or for protecting a human or an animal against the disease symptoms associated with Bordetella infection.
  • the invention further relates to a method for treating a human or an animal against Bordetella infection and/or symptoms associated to disease caused by Bordetella infection, which comprises administering the medicament of the subject invention to such human or animal.
  • Another aspect of the invention is a polypeptide capable of binding to CD11b/CD18 integrin, said polypeptide being either
  • the Bordetella adenylate cyclase is preferably selected among Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica , and more preferably Bordetella pertussis.
  • polypeptides of the invention will be selected among those which adopt an appropriate conformation to bind to the CD11b/CD 18.
  • the polypeptides of the invention may comprise other accessory regions of the Bordetella adenylate cyclase, which are involved in optimal binding to CD11b/CD18.
  • the regions include more specifically, amino acid sequences comprised in the region extending from 1416 to 1648.
  • the polypeptide of the invention is a variant as defined above in b., consisting of one or more fragments from 10 to 50 amino acids of the CD11b/CD18 interaction domain.
  • said polypeptide comprises at least fragments from 10 to 50 amino acids of the region of B. pertussis adenylate extending from amino acid 1208 to amino acid 1243 of B. pertussis adenylate cyclase.
  • Percentage identity corresponds to the percentage of amino acids of the variant sequence which are identical to the wild-type sequence when both sequences are aligned using the BLAST algorithm.
  • the expression “retains the capacity to bind to CD11b/CD18” means that the variant retains at least 80% of the binding affinity to CD11b/CD18 as compared to the wild-type corresponding fragment from which it can be aligned, and preferably, at least 90% of the binding affinity to CD11b/CD18.
  • said polypeptide is specifically reactive with antisera recognizing Bordetella wild-type adenylate cyclase, preferably Bordetella pertussis adenylate cyclase. More preferably, said polypeptide is capable, when administered to a mammal, of raising antibodies recognizing specifically Bordetella adenylate cyclase.
  • said polypeptide is a fragment of the Bordetella pertussis adenylate cyclase.
  • said polypeptide essentially consists of the CD11b/CD18 interaction domain, and more specifically to CD11b/CD18 interaction domain of B. pertussis , extending from amino acid 1166 to amino acid 1281 of B. pertussis adenylate cyclase (SEQ ID NO:2).
  • said polypeptide further comprises an acylation domain of the Bordetella adenylate cyclase and/or the hydrophobic domain.
  • Said acylation domains are included in the corresponding regions extending from residue 700 to residue 1000 of SEQ ID NO: 1, as described in WO 93/21324 and comprise Lys 983 and/or Lys 860.
  • the hydrophobic domain corresponds to the region extending from residue 500 to residue 700 of SEQ ID NO: 1.
  • said polypeptide is not toxic when administered in vivo to a mammal.
  • polypeptides of the invention compete for the binding of the CD11b/CD18 integrin with wild-type adenylate cyclase.
  • the invention thus relates to the use of the polypeptide as defined above, in the preparation of a vaccine or a medicament for the prevention or treatment, in human or in an animal, of disease symptoms associated with whooping cough and/or for protecting a human or an animal against the disease associated with Bordetella infection.
  • the invention concerns the use of said polypeptide of the invention to generate protective antibodies against Bordetella infection.
  • adenylate cyclase is an efficient molecule delivery vector capable of targeting different antigens to dendritic cells leading especially to the generation of potent CD4+ as well as CD8+ T cell responses (EP1188446, Institut Pasteur).
  • the present invention now relates to the use of the polypeptides of the invention, in the preparation of a vector for targeting a molecule of interest, specifically to CD11b expressing cells.
  • polypeptide when used as a vector for a molecule of interest, is directed preferentially to CD11b expressing cells according to the high binding affinity of the CD11b/CD18 interaction domain with the CD11b/CD18, thereby offering means to target the molecule of interest at the surface of said cells or within said cells in a selective way with respect to other cells.
  • the targeting of said molecule or peptide is effective in vivo.
  • the targeting of said molecule is effective in vitro or ex vivo.
  • in vitro it is meant that the target cells are cells, which are cultured in vitro.
  • ex vivo it is meant that the target cells are cells, which have been extracted from a living organism, are cultured in vitro and are intended to be readministered in a living organism.
  • the invention thereby provides means appropriate for the design of compositions suitable for administration to animal or human hosts requiring targeting of certain leukocytes and in particular myeloid dendritic cells, neutrophils or macrophages.
  • the invention more specifically relates to a vector for targeting a molecule of interest to CD11b expressing cells, characterized in that said vector comprises the polypeptide capable of binding to CD11b/CD18, as defined above, coupled to said molecule of interest.
  • the invention also relates to a method for in vitro targeting a molecule of interest to CD11b expressing cells, said method comprising:
  • the invention also provides CD11b-expressing cells comprising a molecule of interest as obtainable by the above-defined method.
  • the expression “molecule of interest” refers to any molecule, preferably a molecule which is not a fragment of a Bordetella species adenylate cyclase.
  • the molecules of interest can also be selected among the nucleic acids, such as DNA, RNA, oligonucleotides, antisense DNA, plasmids and cosmids. They can also be selected among the peptides or polypeptides, and especially, the enzymes, co-enzymes, receptor ligands, haptens, antigens, antibodies and fragments thereof. Naturally, the person skilled in the Art will select the appropriate molecule depending upon the desired use.
  • Molecules of interest can be selected among the active principle of the medicament, the immunotoxins, the antioxidants, the antibiotics, the growth factors, the intracellular hormones, the cytokines, the toxins, the neuromediators, the antimicrobial agents, especially, antiviral, antibacterial, antiparasital or antitumoral and more generally, any therapeutical or prophylactic agent of interest.
  • a molecule of interest is selected among the group consisting of: peptides, glycopeptides, lipopeptides, polysaccharides, oligosaccharides, nucleic acids, lipids and chemicals.
  • a molecule of interest is a heterologous antigen or epitope, the term “heterologous” referring to an antigen or epitope other than the adenylate cyclase antigenic determinant comprised in the vector itself.
  • the molecule of interest is coupled to the polypeptide of the invention to provide the vector of the invention.
  • the term “coupled” means any interaction allowing physical association of the molecule of interest and the polypeptide.
  • the coupling is covalent. It can be direct covalent coupling or indirect coupling by the use of a linkage agent to form a conjugate.
  • Chemical linkage methods are well known in the Art. Chemical linkage can be selected for example among maleimide, peptidic, disulfide or thioether linkage. For example, disulfide linkage using N-pyridyl sulfonyl-activated sulfhydryl can be used.
  • One specific method consists in adding a linker to the polypeptide, said linker consisting of at least one cysteine which can be easily used for disulfide linkage.
  • Another approach consists of coupling chemically a biotinyl moiety, which enables the coupling of other molecules associated to streptavidin.
  • Multiple molecules can be chemically coupled to the polypeptide of the invention by means of a disulfide bond to different cysteine residues, provided that the coupling does not prevent interaction with the CD11b/CD18.
  • the functional properties of the CD11b expressing cells define furthermore a use of said polypeptides of the invention in the manufacturing of a proteinaceous vector for drug targeting to these specific cells.
  • the so-called molecule of interest is an active principle of a medicament. Said active principle may be chemically or genetically coupled to the polypeptide of the invention.
  • a molecule of interest is an anti-inflammatory drug which is, when coupled to the adenylate cyclase toxin, specifically targeted to the surface of the cells involved of the inflammatory response, such as neutrophils.
  • the vector of the invention is more specifically designed to prime CD4+ and CD8+ cells response, said response following the targeting of the molecule of interest to CD11b expressing cells, in particular myeloid dendritic cells.
  • the molecule of interest is or comprises preferably an epitope or an antigen. More specifically, the molecule of interest can be especially an antigen selected from the group consisting of: a poliovirus antigen, an HIV virus antigen, an influenza virus antigen, a lymphocytic choromeningitidis virus, eptitope, a human papillomavirus (HPV) antigen, a bacterial antigen, a mycobacterium tuberculosis antigen for instance.
  • a poliovirus antigen an HIV virus antigen
  • influenza virus antigen an influenza virus antigen
  • eptitope eptitope
  • HPV human papillomavirus
  • the invention thus provides means to prime CD4+ and CD8+ cells response in a patient, either by in vivo targeting antigen or epitope to CD11b expressing cells or by ex vivo targeting antigen or epitope to extracted CD11b expressing cells and re-administering the resulting cells to said patient.
  • the invention relates to a method for in vitro targeting an antigen or an epitope to CD11b expressing cells, said method comprising
  • CD11b-expressing cells extracted from a living organism are myeloid dendritic cells.
  • the invention also provides CD11b-expressing cells comprising a heterologous antigen or epitope obtainable by the above-defined method.
  • the invention thus relates to a cell therapy product for immunizing a human or an animal against an antigen, characterized in that it comprises an efficient amount of CD11b expressing cells comprising a heterologous antigen or epitope obtainable by the above-defined method, in combination with a pharmaceutically acceptable vehicle.
  • the invention further relates to a use of CD11b-expressing cells comprising said antigen or epitope as obtainable by the above-defined method, in the preparation of a cell therapy product for immunizing a human or an animal against an antigen.
  • the invention provides a method for immunizing a patient against an antigen, said method comprising:
  • said CD11b-expressing cells are myeloid dendritic cells.
  • the invention thus also relates to the pharmaceutical composition
  • the pharmaceutical composition comprising the vector of the invention carrying an epitope or an antigen as the molecule of interest, in combination with a pharmaceutically acceptable vehicle.
  • said composition is a vaccine suitable for administration in a human or an animal.
  • the vaccine is capable of inducing immunity against poliovirus, HIV or a lymphocytic choromeningitidis virus.
  • the type of immunity induced will depend upon the selected antigen which is carried by the vector.
  • the vaccine is capable of inducing immunity against whooping cough.
  • Such vaccines comprise an immunoprotective and non-toxic amount of the vector of the invention.
  • Said composition may further comprise suitable priming adjuvants accordingly.
  • the invention further relates to a method for immunizing a human or an animal against a pathogen infection, which comprises administering the vaccine comprising an immunoprotective and non toxic amount of the vector of the subject invention to such human or animal.
  • the invention is also directed to the means for preparing the polypeptides, proteins or the vector of the invention.
  • those means comprise a nucleic acid encoding one of the following polypeptides:
  • Modifications of the wild-type DNA encoding Bordetella adenylate cyclase can be obtained by genetic engineering of the wild-type DNA using conventional molecular biology technologies.
  • Another object of the invention concerns a recombinant nucleic acid constituted by the nucleic acid encoding the polypeptide, the protein or the vector of the invention, cloned into an expression vector appropriate for the expression of the encoded polypeptide or protein in a host cell.
  • the recombinant DNA molecule comprise additional coding sequence of a carrier polypeptide which has immunostimulating properties, such as an adjuvant, or which is useful in expressing, purifying and/or formulating the polypeptides of the invention.
  • This coding sequence can be placed in frame with the coding sequence of the polypeptide, protein or vector for targeting molecule of the invention.
  • the selection of the expression vector will, of course, depend upon the host cell employed.
  • said expression vector is a plasmid, a cosmid, a phagemid or a viral DNA.
  • the invention is also directed to a method for preparing the protein of the invention deficient for CD11b/CD18 binding; the polypeptide capable of binding CD11b/CD18 as defined above; or the vector for targeting a molecule of interest to CD11b expressing cells, said method comprising the steps of incorporating the recombinant nucleic acid as defined above in an appropriate host cell for the expression of the corresponding polypeptide, protein or vector of interest; culturing the transformed recombinant cells and recovering the synthesized recombinant polypeptide, protein or vector of the invention.
  • Another aspect of the invention is a host cell transformed with the recombinant nucleic acid of this invention and thus comprising the nucleic acid or the recombinant nucleic acid as defined above.
  • the recombinant nucleic acid can be integrated into the host cell's genome by conventional techniques, including homologous recombination.
  • Preferred host cells of the invention include those belonging to the species E. coli and the genus Bordetella .
  • Other host cells which may be suitable include, but are not limited to, mammalian cells, insect cells, yeast and other bacterial cells.
  • the invention also encompasses the polyclonal serum obtainable by the immunization of an animal or a human with the polypeptide, the protein, the vector or with the composition of the invention.
  • the polyclonal serum is obtainable by the immunization of an animal or a human with the polypeptide consisting of the CD11b/CD18 interaction domain of Bordetella adenylate cyclase, preferably the CD11b/CD18 interaction domain of Bordetella pertussis adenylate cyclase, extending from amino acid 1166 to amino acid 1281.
  • the invention also relates to monoclonal antibody directed specifically against the polypeptides of the invention comprising the CD11b/CD18 interaction domain.
  • the monoclonal antibody is directed against an epitope located in the CD11b/CD18 interaction domain, preferably against an epitope located in the CD11b/CD18 interaction domain of Bordetella pertussis adenylate cyclase, extending from amino acid 1166 to amino acid 1281.
  • said polyclonal serum, or monoclonal antibody is capable of blocking the binding of wild-type adenylate cyclase to CD11b/CD18.
  • the blocking can be assayed by evaluating the capacity of a mixture of said polyclonal serum or monoclonal antibody with a wild-type adenylate cyclase to bind to CD11b/CD18 as compared to the capacity of wild-type adenylate cyclase alone.
  • said medicament provides passive immunization against Bordetella infection.
  • the antibodies of the invention can be humanized for instance by the replacement of the hypervariable part of a human immunoglobulin, which has no antibody function, by a hypervariable region of a monoclonal immunoglobulin obtained from the technique described above.
  • the invention also concerns a pharmaceutical composition, comprising the polyclonal serum or the monoclonal serum, in combination with a pharmaceutically acceptable vehicle.
  • the invention also relates to the use of a polyclonal serum or a monoclonal antibody of the invention, in the preparation of a medicament for the treatment, in human or in animal, of disease symptoms associated with whooping cough and/or for protecting a human or an animal against the disease symptoms associated with Bordetella infection.
  • the following experimental part shows the results identifying (i) the role of post-translational acylation in CyaA interaction with CD11b and (ii) the CD11b interaction domain in Bordetella pertussis adenylate cyclase.
  • FIG. 1 CyaA binds specifically to CD11b cells and inhibits both CyaA-biotin and anti-CD11b monoclonal antibody binding to these cells
  • CHO-CD11b cells were preincubated with the indicated concentrations of CyaA. Then, CyaA-biotin (30 nM) or anti-CD11b Mab (2 ⁇ g/ml) was added separately in the continuous presence of the toxin and their binding was measured by FACS.
  • FIG. 2 Direct binding of CyaA or proCyaA to CHO tranfectants.
  • CHO-CD11b cells (A) or CHO cells (B) were incubated with the indicated concentrations of CyaA or proCyaA.
  • Surface-bound CyaA was detected with anti-CyaA Mab (5G12).
  • FIG. 3 CyaA acylation is required for stable association with CHO-CD11b cells
  • CHO-CD11b cells were preincubated with the indicated concentrations of CyaA or proCyaA.
  • CyaA-biotin (A) or anti-CD11 b Mab (B) was then added, in the continuous presence of CyaA or proCyaA.
  • FIG. 4 CyaA acylation is required for CyaA induced-cAMP accumulation and cytotoxicity
  • CHO-CD11b cells were incubated with either CyaA or proCyaA at the indicated concentrations for 20 min at 37° C. Then, cells were lysed and cAMP was measured (A). In parallel, toxicity was determined by measuring the amount of lactate dehydrogenase released in the medium after incubation of CHO-CD11b cells for 4 hours at 37° C. in the presence of the indicated concentrations of either CyaA or proCyaA (B). Results are representative of at least 2 independent experiments.
  • FIG. 5 The catalytic domain is not required for CyaA interaction with CD11b cells
  • FIG. 6 Direct binding of CyaA fragments to CD11b cells
  • CHO-CD11b cells A, C
  • CHO cells B, D
  • CHO-CD11b cells A, C
  • CHO cells B, D
  • surface-bound CyaA was detected with anti-CyaA 5G12 Mab that recognizes the catalytic domain (A, B) or with anti-CyaA 6D7 Mab that recognizes the repeat domain (C, D).
  • FIG. 7 CyaA-biotin binding to CHO-CD11b cells in the presence of CyaA-FLAG mutants
  • FIG. 8 SDS-Page analysis of the purified CyaA preparations and their invasive activity on erythrocytes
  • CyaA/FLAG molecules together with the wild type CyaA were purified from urea extracts by DEAE- and Phenyl sepharose chromatographies as previously described (Karimova et al., 1998). About 3 ⁇ g of each protein was analyzed on a 7.5% acrylamide gel stained with Coomassie blue.
  • FIG. 9 CyaA binding to CHO-CD11b cells in the presence of selected CyaA-FLAG mutants
  • DNA manipulations were performed according to standard protocols (Sambrook et al., 1989) in the Escherichia coli strain XL1-Blue (Stratagene, Amsterdam, Netherlands) as host cells.
  • the plasmids coding for a non-acylated wild type proCyaA (pACT7), acylated wild type CyaA (pT7CACT1) and a recombinant detoxified CyaA-E5-CysOVA harbouring a unique cysteine residue and the OVA epitope in its catalytic domain (pCACT-E5-CysOva) were already described (Gmira et al., 2001; Guermonprez et al., 2001; Osicka et al., 2000; Sebo et al., 1991).
  • the plasmid encoding CyaA 373-1706 (pTRCyaA ⁇ 1-373) is a derivative of pTRCAG (Gmira et al., 2001) in which the DNA sequence coding for the catalytic domain of the toxin (comprised between the NdeI and BstBI sites) was deleted and replaced by an appropriate synthetic double stranded oligonucleotide encoding the amino acid sequence: Met-Gly-Cys-Gly-Asn.
  • CyaA-E5-CysOVA protein was labeled on its unique cysteine residue with the sulfhydryl reagent N-(6-(Biotinamido)hexyl)-3′-(2′-pyridyidithio)propiamide (Biotin-HPDP) (Pierce, Bezons, France) according to the manufacturer's instructions.
  • Biotin-HPDP sulfhydryl reagent N-(6-(Biotinamido)hexyl)-3′-(2′-pyridyidithio)propiamide
  • Biotin-HPDP Biotin-HPDP
  • Toxin concentrations were determined spectrophotometrically from the adsorption at 278 nm using a molecular extinction coefficient of 141 mM ⁇ 1 cm ⁇ 1 for the full length CyaA toxins, 113 mM 1 cm ⁇ 1 for the CyaA 373-1706 and 28 mM ⁇ 1 cm ⁇ 1 for CyaA 1-384.
  • CyaA-FLAG molecules were constructed using the previously defined permissive insertion sites along the CyaA molecule (Osicka et al., 2000). We generated a set of 17 CyaA constructs, which carried at the individual permissive positions a synthetic octapeptide insert Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys for the FLAG epitope (Sigma, Saint Quentin Fallavier, France).
  • mice were initially immunized intraperitoneally with CyaA toxin (20 ⁇ g in alum). At approximately two weeks interval, mice were boosted with 10 ⁇ g CyaA in alum for 3 times. Throughout the immunization protocol, mice were bled and their sera tested for the presence of anti-CyaA antibodies by ELISA. When significant sera titers were detected, a last boost was given to these mice and their splenocytes were fused with P3X63 myeloma cells (ATCC, Manassas, USA) 3 days later. The generated hybridomas were screened for the production of CyaA specific monoclonal antibodies by ELISA.
  • the monoclonal antibodies were purified from ascites using T-GelTM purification kit (Pierce, Bezons, France) according to manufacturer instructions. The antibody concentration was measured with Bio-Rad protein assay (Bio-Rad, Marnes la Coquette, France). Two of these monoclonal antibodies were used in this study: antibody 5G12 that reacts with an epitope localized within amino acid 1 to 190, and antibody 6D7 that reacts with an epitope localized within amino acids 1006 to 1706.
  • CHO-CD11b cells Chinese Hamster Ovary cells transfected with human CD11b/CD18 (CHO-CD11b cells), human CD11c/CD18 (CHO-CD11c cells) or transfected with the vector alone (CHO cells) were a kind gift of D. Golenbock (Boston University School of Medicine, Boston, Mass.) and were cultured in the presence of neomycin as described previously (Ingalls et al., 1998).
  • Monoclonal antibodies specific for human CD11b (ICRF44, mouse IgG1, ⁇ ) and human CD11c (B-Ly6, mouse IgG1, ⁇ ) were purchased from BD Pharmingen (Le Pont de Claix, France).
  • the assays were performed as described in Guermonprez et al., 2001. Briefly, 2 ⁇ 10 5 cells were incubated with the indicated concentrations of CyaA molecules in DMEM medium containing 4.5 mg/ml glucose (Life Technologies, Cergy Pontoise, France), without serum, in 96-well culture plates for 30 min on ice. After washing, ant-CyaA catalytic domain Mab (5G12) or anti-CyaA repeat domain Mab (6D7) was added at 25 ⁇ g/ml. In some experiments, cells were preincubated with the indicated concentrations of CyaA molecules for 30 min on ice.
  • CyaA-biotin (30 nM), anti-CD11b Mab (2 ⁇ g/ml) or anti-CD11c Mab (2 ⁇ g/ml) (BD Pharmingen) were added separately in the continuous presence of the toxins.
  • cells were stained with goat anti-mouse IgG-PE (Caltag, Le Perray en Yvelines, France) or with streptavidin-PE (BD Pharmingen) at 1:300 dilution. After the last wash, cells were analyzed by flow cytometry on a FACStarTM (Becton Dickinson, Le Pont de Claix, France) in the presence of 5 ⁇ g/ml propidium iodide. Aggregated and dead cells were substracted by gatings based on propidium idiode exclusion.
  • FACStarTM Becton Dickinson, Le Pont de Claix, France
  • the maximum binding corresponds to (MFI value of cells incubated with CyaA or anti-CD11b in the absence of competitor) ⁇ (MFI value of cells incubated with medium alone).
  • the sample binding corresponds to (MFI value of cells incubated with CyaA or anti-CD11b in the presence of competitor) ⁇ (MFI value of cells incubated with medium alone).
  • Cyclic AMP accumulated in cells exposed to the CyaA toxin was performed essentially as described in Guermonprez et al., 2001. Briefly, 5 ⁇ 10 5 cells were incubated with the indicated concentrations of CyaA in DMEM+glucose for 20 min at 37° C. After washing, cAMP accumulated in cell cytosol was released by lysis with 0.1 N HCl and boiling for 5 min at 120° C. After neutralization with 0.1 N NaOH, the samples were then added to microtiter plates previously coated with a cAMP-BSA conjugate and, then incubated with an appropriate dilution of anti-cAMP rabbit antiserum. After washing, anti-cAMP antibodies were revealed with anti-rabbit antibodies coupled to Alkaline phosphatase. The cAMP content of each sample was determined from comparison with a standard curve obtained by adding known cAMP concentration.
  • Invasive activity of CyaA molecules was determined as described previously in Osicka et al., 2000. Briefly, sheep erythrocytes were incubated with toxin for 30 min and the invasive activity was measured as the AC activity translocated into erythrocytes and protected against digestion by extracellularly added trypsin.
  • CyaA binding assay was specifically detected on CD11b + cells.
  • CyaA molecules can be tested for their ability to compete with CyaA-biotin, or anti-CD11b monoclonal antibody (Mab) binding to CD11b + cells.
  • CyaA-biotin or anti-CD11b monoclonal antibody (Mab) binding to CD11b + cells.
  • CyaA-biotin (30 nM) or anti-CD11b Mab (2 ⁇ g/ml) were added and their binding to the cells was evaluated by FACS.
  • CyaA efficiently inhibited both CyaA-biotin and anti-CD11b binding to CHO-CD11b cells in a dose dependent manner. This inhibitory effect was specific for CD11b since CyaA was completely unable to compete with another ligand (anti-CD11c Mab) for its specific receptor (CD11c) expressed by CHO cells ( FIG. 1C ).
  • CyaA needs a postranslational palmitoylation to perform its invasive activity and to form hemolytic membrane channels.
  • CyaA needs a postranslational palmitoylation to perform its invasive activity and to form hemolytic membrane channels.
  • a binding assay CHO cells or CHO-CD11b cells were incubated with either CyaA or non acylated proCyaA. The binding was evaluated using anti-CyaA catalytic domain Mab (5G12). As shown in FIG. 2A , at low concentrations, binding of both CyaA and proCyaA molecules to CD11b + cells was rather comparable, with a slightly more efficient binding of the acylated CyaA.
  • CyaA is composed of two main domains harboring independent activities.
  • the N-terminal domain harbors the adenylate cyclase activity (aminoacids 1-400), whereas the carboxy-terminal hemolysin moiety (aminoacids 400-1706) is responsible for the delivery of the AC domain into target cells and the hemolytic activity of B. pertussis .
  • the 17 FLAG-tagged CyaA molecules were expressed and purified to homogeneity and tested for the capacity to inhibit binding of CyaA-biotin to CHO-CD11 b cells (note that in two cases, CyaA ⁇ 510-515/FLAG and CyaA ⁇ 1245-1273/FLAG, the amino acids 510 to 515 or 1245 to 1273 of CyaA, respectively were deleted and replaced by the inserted FLAG epitope).
  • insertion of the FLAG epitope at 3 different sites located between residues 1166-1281 totally abrogated the interaction with CD11b.
  • the corresponding modified CyaA were essentially unable to compete with CyaA-biotin for CD11b binding, when tested at 30 nM concentrations.
  • CyaA domain that interacts with CD11b
  • These CyaA molecules were again expressed and purified close to homogeneity ( FIG. 8A ) and their cell-invasive activity was examined by analyzing their capacity to penetrate sheep erythrocyte membranes (RBC) and to deliver the catalytic domain into a compartment inaccessible to externally added trypsin. As shown in FIG.
  • CyaA1387/FLAG the invasive activity of all other tested CyaA/FLAG molecules was affected to some extent by insertion of the FLAG peptide.
  • the invasive activity of CyaA524/FLAG which reflects the capacity of CyaA to translocate the catalytic domain into erythrocytes, was completely ablated by the insertion of the FLAG peptide at residue 524.
  • the capacities of the other proteins, CyaA424/FLAG, CyaA722/FLAG and CyaA1166/FLAG and, to a lesser extent, of CyaA ⁇ 1245-1273/FLAG and CyaA1281/FLAG proteins to penetrate into RBC were, however, comparable.
  • CyaA-biotin binding to CD11b + cells was tested in a dose dependent manner, as shown in FIG. 9 .
  • the CyaA1166/FLAG, CyaA ⁇ 1245-1273/FLAG, and CyaA1281/FLAG proteins were unable to inhibit CyaA-biotin binding to CD11b + cells, even at concentrations as high as 240 nM.
  • all other CyaA/FLAG constructs inhibited the CyaA-biotin binding in a dose dependent manner, similarly to intact CyaA.
  • ACT adenylate cyclase toxin
  • CyaA cannot deliver its catalytic domain into erythrocyte cytosol and is unable to form hemolytic channels (Barry et al., 1991; Basar et al., 2001;hackett et al., 1994). CyaA was shown to penetrate with detectable efficiency a large variety of eukaryotic cells.
  • CyaA acylation plays a major role in its interaction with CD11b + cells. Indeed, albeit non-acylated proCyaA was able to bind CD11b + cells as efficiently as CyaA, it was inefficient in competing with acylated CyaA for binding to CHO-CD11b + cells and was completely unable to block anti-CD11b Mab binding to these cells. This suggests that while still interacting with CD11b, the nature of interaction and in particular the affinity and/or stability of the proCyaA-CD11b complex differs significantly from that involved in CD11b interaction of the mature CyaA.
  • proCyaA is still able to bind the CD11b receptor, this interaction does not allow membrane penetration of the protoxin.
  • the acylation may be needed to confer a translocation-competent conformation of CyaA that is required for the delivery of the catalytic domain to the cell cytosol where it can catalyze the conversion of ATP to cAMP.
  • CyaA can be divided in two main domains; one endowed with adenylate cyclase activity domain located between residues 1 to 400, and one responsible for hemolytic activity located within residues 400 to 1706 (Ladant and Ullmann, 1999).
  • the catalytic domain can be directly translocated across the plasma membrane of erythrocytes.
  • the present data show that albeit the catalytic domain plays a key role in the cytotoxic activity of CyaA by catalyzing conversion of ATP to cAMP, this domain is not required for binding of CyaA to its receptor.
  • CyaA has been used in several passive and active protection protocols in mouse models of pertussis. Immunization with anti-CyaA specific antibodies or with purified CyaA reduced the time course of the respiratory tract colonization by B. pertussis and protected the mice against a lethal intranasal infection (Guiso et al., 1989; Guiso et al., 1991). Moreover, antibodies specific for CyaA were detected in the sera of human infants infected with B. pertussis (Arciniega et al., 1991; Guiso et al., 1993). The present results suggest that a CyaA molecule lacking CyaA/CD11b interaction domain can be designed for the production as a safe acellular vaccine for protection against B.
  • the catalytic activity of such a molecule can be easily inactivated by dipeptide insertions within the ATP-binding site, located between residues 188 and 189 of CyaA (Fayolle et al., 1996), while the deletion within the CD11 b interaction domain could preserve immune cells from potentially negative effects, such as signaling upon the integrin engagement by the toxoid and/or some functional interference due to competition for binding to CD11b with the CyaA toxoid, which also serves as the complement receptor CR3.
  • the present data provide important new insights into the role of acylation and of different domains of the adenylate cyclase of B. pertussis in its interaction with CD11b + cells as well as in the subsequent biological activities triggered by this interaction.

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EP1489092A1 (en) 2003-06-18 2004-12-22 Institut Pasteur Modified Bordetella adenylate cyclase comprising or lacking CD11b/CD18 interaction domain and uses thereof

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US7906123B1 (en) 2003-06-18 2011-03-15 Institut Pasteur Modified Bordetella adenylate cyclase comprising or lacking CD11b/CD18 interaction domain and uses thereof
US20100063099A1 (en) * 2007-01-12 2010-03-11 Lonny Levin Adenylyl cyclases as novel targets for the treatment of infection by eukaryotic pathogens
US20100168203A1 (en) * 2007-01-12 2010-07-01 Lonny Levin Adenylyl cyclases as novel targets for antibactrial interventions
US9017681B2 (en) * 2007-01-12 2015-04-28 Cornell Research Foundation, Inc. Adenylyl cyclases as novel targets for antibactrial interventions
US9095578B2 (en) 2007-01-12 2015-08-04 Cornell Research Foundation, Inc. Adenylyl cyclases as novel targets for the treatment of infection by eukaryotic pathogens
US10494407B2 (en) 2010-09-20 2019-12-03 Wisconsin Alumni Research Foundation Mosquitocidal xenorhabdus, lipopeptide and methods
WO2016094438A1 (en) * 2014-12-08 2016-06-16 Board Of Regents, The University Of Texas System Bordetella adenylate cyclase toxin vaccines and neutralizing antibodies

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JP2007527697A (ja) 2007-10-04
EP1633776A1 (en) 2006-03-15
AU2004249431A1 (en) 2004-12-29
RU2421241C2 (ru) 2011-06-20
BRPI0411510A (pt) 2006-07-25
EP1633776B1 (en) 2017-08-09
AU2004249431B2 (en) 2009-11-05
RU2006101326A (ru) 2006-07-27
CA2529565A1 (en) 2004-12-29
JP4824550B2 (ja) 2011-11-30
EP1489092A1 (en) 2004-12-22
US7906123B1 (en) 2011-03-15
WO2004113372A1 (en) 2004-12-29
KR20060034645A (ko) 2006-04-24

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