Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
• • 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
  • A61K39/095—Neisseria
• • 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
  • 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
  • A61K2039/55555—Liposomes; Vesicles, e.g. nanoparticles; Spheres, e.g. nanospheres; Polymers

Definitions

• This invention relates to broad-spectrum vaccines for the prevention of diseases caused by Neisseria meningitidis, especially serogroup B.
• Neisseria meningitidis is a Gram-negative bacteria which colonizes the human upper respiratory tract and is responsible for worldwide sporadic and cyclical epidemic outbreaks of, most notably, meningitis and sepsis. The attack and morbidity rates are highest in children under 2 years of age.
• Neisseria meningitidis typically possess a cytoplasmic membrane, a peptidoglycan layer, an outer membrane which together with the capsular polysaccharide constitute the bacterial wall, and pili which project into the outside environment. These surface structures mediate infection and interact with the host immune system. For example, a first step in infection with Neisseria is adherence to target cells, which is thought to be mediated by the pili and, possibly, other adhesins such as Ope.
• Protein, phospholipid and polysaccharide components of the outer membrane have been reported to elicit an immune response.
• Neisseria meningitidis spp. can be divided into serologic groups, types and subtypes on the basis of reactions with polyclonal (Frasch, C. E. and Chapman, 1973, J. Infect. Dis.
• Serogrouping is based on immunologically detectable variations in the capsular polysaccharide. About 12 serogroups are known: A, B, C, X, Y, Z, 29-E, W-135, H, I, K and L (Ashton, F. E. et al., 1938, J. Clin. Microbiol. 17: 722-727; Branham, S. E., 1956, Can. J. Microbiol. 2: 175-188; Evans, A. C, 1920, Lab. Bull. 1245: 43-87; Shao-Qing, et al., 1972, J. Biol. Stand.
• Serotyping is based on monoclonal antibody defined antigenic differences in an outer membrane protein called Porin B (PorB). Antibodies defining about 21 serotypes are currently known (Sacchi et al, 1998, Clin. Diag. Lab. Immunol. 5:348). Serosubtyping is based on antibody defined antigenic variations on an outer membrane protein called Porin A (PorA). Antibodies defining about 18 serosubtypes are currently known. Serosubtyping is especially important in Neisseria meningitidis strains where immunity may be serosubtype specific. Most variability between PorA proteins occurs in two (loops I and IV) of eight putative, surface exposed loops. The variable loops I and IV have been designated VRl and VR2, respectively.
• Neisseria meningitidis also may be divided into clonal groups or subgroups, using various techniques that directly or indirectly characterize the bacterial genome. These techniques include multilocus enzyme electrophoresis (MLEE), based on electrophoretic mobility variation of an enzyme, which reflects the underlying polymorphisms at a particular genetic locus. By characterizing the variants of a number of such proteins, genetic "distance" between two strains can be inferred from the proportion of mismatches. Similarly, clonality between two isolates can be inferred if the two have identical patterns of electrophoretic variants at number of loci.
• MLEE multilocus enzyme electrophoresis
• MLST multilocus sequence typing
• the polysaccharide capsule is one of the outermost structures of pathogenic Neisseria meningitidis, it has been a primary focus of attempts to develop vaccines.
• Different preparations of capsular polysaccharides have been used to control the outbreaks and epidemics of the serogroups A, C, Y and W-135, as mono-, di-, tri- or tetravalent vaccines (Gold et al., 1969-1970, Bull. WHO 45: 272-282; Gotschlich et al., 1969, J. Exp. Meal. 129: 134-136; Hankins, 1982, Proc. Soc. Biol. Med. 169: 54-57; U.S. Pat. No. 6,080,589).
• capsular polysaccharide vaccines suffer from: poor or no-response to polysaccharide C in children under 2 years of age; thermolability of polysaccharide A; difficulties regarding the induction of immunologic tolerance after vaccination or re-vaccination with polysaccharide C (Granoff et al., 1998, J. Infect. Dis. 160: 5028-5030; MacDonald et al., 1998, JAMA 280:1685-1689; MacDonald et al., 2000, JAMA 283: 1826- 1827). To circumvent these immunologic properties, polysaccharides from serogroups A and C have been covalently coupled to protein carriers to make "conjugate" vaccines.
• conjugate vaccines are highly immunogenic in infants, upon re-injection elicit boostable increases in serum anticapsular antibody concentrations, and prime for the ability to generate memory antibody responses to a subsequent injection of plain polysaccharide (Campagne et al. 2000, Pediat. Infect. Dis. J. 19: 144-150; Maclennan et al., 2000, JAMA 283: 2795-2801).
• Conjugate vaccines with similar properties have been highly effective in preventing invasive diseases caused by other encapsulated bacteria, such as Haemophilus influenzae type b or Streptococcus pneumoniae.
• the capsular polysaccharide (PS) of serogroup B Neisseria meningitidis is a very poor immunogen in humans (Wyle et al., 1972, J. Infect. Dis. 126: 514-522; Zollinger, et al., 1979, J. Clin. Invest. 63: 836-834; Jennings et al., 1981, J. Immunol. 127: 104-108). Further attempts to improve the polysaccharide' s immunogenicity through conjugation to protein have been unsuccessful (Jennings et al., 1981, J. Immunol. 127: 104-108).
• the meningococcal serogroup B capsule polysaccharide (MenB PS) has been chemically modified (N-propionylated group was substituted for the N-acetyl group of B polysaccharide) and coupled covalently to a protein carrier (N-Pr-MenB PS-protein) conjugate.
• the vaccine induces in mice high titers of IgG antibodies which are bactericidal and protective (this concept is described and claimed in U.S. Patent No. 4,727,136, issued Feb. 23, 1988 to Jennings et al.).
• This vaccine also is immunogenic in sub-human primates, inducing serum antibodies that activate complement-mediated bacteriolysis (Fusco et al., 1997, J.
• NspA Neisserial surface protein A
• host polysialic acid i.e. serogroup B
• high antigenic mutability for the immunodominant noncapsular epitopes i.e. epitopes of antigens that are present at the surface in relatively large quantities, are accessible to antibodies, and elicit a strong antibody response.
• the present invention generally provides methods and vaccines for the prevention of diseases caused by Neisseria meningitidis bacteria, particularly serogroup B strains.
• the method of the invention comprises: administering to a mammal a first preparation of i) outer membrane vesicles (OMV) of a first Neisseria meningitidis spp., and/or ii) microvesicles (MV) released into a culture medium during culture of a first Neisseria meningitidis spp., said administering of OMV and/or MV being in a sufficient amount to immunologically prime and/or elicit an immune response to epitopes present in said first preparation; administering at least a second preparation of i) OMNs of a second Neisseria meningitidis spp., and/or ii) MNs released into a culture medium during culture of a second Neisseria mei ⁇ ingitidis spp., said administering of
• third preparation results in induction of an immune response to epitopes present in the preparations, wherein said response confers protective immunity against a disease caused by Neisseria meningitidis spp.
• the first, second, and third Neisseria strains are genetically diverse to one another, e.g., the first strain is genetically diverse to the second strain, the third strain, or both the second and third strain.
• administration of the preparations is serial.
• Serial administration of the preparations can be conducted in any order.
• the following orders of administration are within the scope of the invention (from left to right, with the third administration being optional): OMN-OMN-OMV; OMN-OMN-MN; OMN- MV-MV; MV-MV-MV; MN-MN-OMV; MV-OMV-OMV; OMV-MV-OMV; and MV- OMV-MV.
• the order of administration is MV-MV-OMV.
• the preparations are administered as a mixture, where the initial administration of the mixture can be followed by one or more additional administrations of the same or different mixture to serve as boosters.
• the invention involves serially administering microvesicles (MN) that bleb naturally during growth of Neisseria meningitidis and are released in the culture medium (collected by separating the larger cells from the smaller blebs and then pelleting the blebs) and/or outer membrane vesicles (OMN, prepared directly from isolated outer membrane fractions).
• MN microvesicles
• OMN outer membrane vesicles
• Neisseria meningitidis for example, strains that differ from one another in at least one of serotype or serosubtype, and may be diverse at multiple genetic loci, e.g., differ in both serotype and serosubtype, e.g., having different outer membrane Porin, PorA and PorB proteins.
• the OMN and/or MN preparations can be given sequentially in at least two, and preferably at least three administrations (e.g., injections) of OMNs or MNs from genetically diverse strains; four, five, six or more administrations are also contemplated.
• the second Neisseria meningitidis spp. is a member of a second serosubtype, which second subserotype are different from the subserotype of the first Neisseria meningitidis spp, and, where used, the third Neisseria meningitidis spp. is a member of a third serosubtype, which third subserotype is different from the subserotype of at least the first, and preferably both the first and the second, Neisseria meningitidis spp.
• the first Neisseria meningitidis spp. is a member of a first serotype and of a first serosubtype;
• the second Neisseria meningitidis spp. is a member of a second serotype and of a second serosubtype, which second serotype and second subserotype are different from the serotype and subserotype of the first Neisseria meningitidis spp, and, where used, the third Neisseria meningitidis spp.
• spp is a member of a third serotype and of a third serosubtype, which third serotype and third subserotype are different from the serotype and subserotype of at least the first, and preferably both the first and the second, Neisseria meningitidis spp.
• a first administration is with microvesicles (MNs) prepared from a serogroup C strain (e.g. RM1090 (C:2a:P1.5,2:L3,7)).
• the second administration is with MNs prepared from a second strain (e.g. BZ198 (B: ⁇ T:P1.4)), and the third administration is with outer membrane vesicles (OMNs) prepared from a third strain (e.g. Z1092 (A: 4,21 :P1.10)).
• CHORI vaccine Sequential immunization with vesicles and/or microvesicles prepared from genetically diverse Neisseria meningitidis strains is referred to hereafter as the "CHORI vaccine” or "CHORI antigen.” Immunization with a mixture of the first, second, and third preparations of the CHOR vaccine is referred to as "CHORI mix”.
• the invention features a composition
• a composition comprising a first preparation selected from the group consisting of outer membrane vesicle (OMV), microvesicles (MV), or both OMN and MN from a first from a first Neisseria meningitidis species; a second preparation selected from the group consisting of outer membrane vesicle (OMV), microvesicles (MN), or both OMN and MV from a second Neisseria meningitidis species, wherein the second Neisseria meningitidis spp is genetically diverse to the first Neisseria meningitidis species; and a pharmaceutically acceptable carrier.
• a first preparation selected from the group consisting of outer membrane vesicle (OMV), microvesicles (MV), or both OMN and MN from a first from a first Neisseria meningitidis species
• a second preparation selected from the group consisting of outer membrane vesicle (OMV), micro
• the composition further comprises a third preparation selected from the group consisting of outer membrane vesicle (OMV), microvesicles (MN), or both OMV and MN from a third Neisseria meningitidis species, wherein the third Neisseria meningitidis species is genetically diverse to the first Neisseria meningitidis species.
• OMV outer membrane vesicle
• MN microvesicles
• the third preparation comprises OMV.
• the first and second Neisseria meningitidis species are genetically diverse in that they differ in at least one of serotype or serosubtype, and, where included, the third and the first Neisseria meningitidis species are genetically diverse in that they differ in at least one of serotype or serosubtype.
• the invention features a composition
• a composition comprising at least one isolated Neisseria meningitidis antigen, the isolated antigen being present in the composition in an amount effective to elicit an immune response in a mammalian host, and being characterized as a protein immunoprecipitated with anti-sera produced following vaccination with the CHORI-vaccine, and having an apparent molecular mass selected from the group consisting of about 80 kDa, about 59.5 kDa, about 40.7 kDa. about 39.6 kDa, about 33 kDa, about 27.9 kDa, and 14.5 kDa; and a pharmaceutically acceptable excipient.
• the invention features a composition
• a composition comprising at least one isolated Neisseria meningitidis antigen, the isolated antigen being present in the composition in an amount effective to elicit an immune response in a mammalian host, and being characterized as a protein detected by Western blot with anti-sera produced following vaccination of a mammal with the CHORI vaccine, and having an apparent molecular mass selected from the group consisting of about 53 kDa to 57 kDa; about 46-47 kDa, about 33 kDa, about 20 kDa to 21 kDa; and about 18 kDa; and a pharmaceutically acceptable excipient.
• the invention features a composition
• a composition comprising at least one isolated Neisseria meningitidis antigen, the isolated antigen being present in the composition in an amount effective to elicit an immune response in a mammalian host, wherein the antigen is from a protein that specifically binds a monoclonal antibody selected from the group consisting of 1D9, 4B11, 9B8, and 14C7 (which antibodies are described herein and deposited with the ATCC); and a pharmaceutically acceptable excipient.
• the compositions having isolated antigens comprise at least two isolated Neisseria meningitidis antigens.
• the invention features methods for eliciting broad spectrum protective immunity against a disease caused by a Neisseria meningitidis species, said method comprising administering to a mammal at least one of the compositions comprising isolated antigens as described above.
• the antigen compositions may be administered to mammals, especially humans, that are immunologically na ⁇ ve with respect to Neisseria meningitidis (i.e., have not been exposed to antigens from Neisseria meningitidis, or have not been exposed insufficient amounts to elicit a protective immune response).
• a specific embodiment of the invention involves administration to human infants that are about five years old or younger, especially two years old or younger.
• the individuals prior to administration of antigen compositions from Neisseria meningitidis, the individuals may have been primed by exposure (through natural infection or administration) to a Neisserial species other than Neisseria meningitidis (or an antigen composition prepared from a Neisserial species).
• Antisera obtained from mice immunized as described above bind to the bacterial cell surface of a group of genetically diverse Neisseria meningitidis serogroup B strains, as determined by flow cytometric detection of indirect immunofluorescence.
• sera from immunized mice were positive for eleven of 12 strains tested. These 11 included 3 meningococcal B strains with respective PorA and PorB proteins that were heterologous to those of the meningococcal strains used to prepare the immunogens used for vaccination.
• antisera from animals immunized with two injections of the above- described "Norwegian OMV vaccine" reacted by flow cytometry with only 5 of 11 strains.
• Antisera from mice immunized in a second example using the CHORI vaccine were bactericidal against 14 of 14 strains tested including eight strains with serosubtypes that were heterologous from those used in the vaccine preparations.
• antisera prepared from guinea pigs immunized with the CHORI vaccine were bactericidal against 9 of 10 strains tested including 5 strains with serosubtypes that were heterologous to those expressed by the vaccine strains.
• Antisera to the CHORI vaccine prepared in mice in the first example and in guinea pigs in the third example also were highly protective against bacteremia in the infant rats challenged with serogroup B bacteria.
• the immunization protocol used herein generally induces the immune system to converge on non-capsular antigens that are common to the strains from which the MNs and OMNs are obtained.
• the CHORI vaccine elicits antibodies against multiple cell surface epitopes, including, PorA, possibly PorB, and conserved proteins such as Neisserial surface protein A (NspA), the class 4 protein, (reduction modifiable protein, Rmp) and other noncapsular antigens as yet unidentified.
• NspA Neisserial surface protein A
• Rmp reduction modifiable protein
• the vaccines of the present invention that employ sequential immunization with antigenic material prepared from different strains (genetically diverse) have the potential to confer protection against the majority of eisseria meningitidis serogroup B strains. This approach also has broad applicability for vaccination against Neisseria meningitidis strains representative of other serogroups such as A, C, Y, or W-135, and also against other members
• Figure 1 summarizes the results of meningococcal outer membrane vesicle vaccine efficacy trials.
• Figure 2 is a photograph of a 15% SDS-PAGE gel of microvesicle (MV), deoxycholate extracted microvesicle (DOC MV), outermembrane vesicle (OMV), and deoxycholate extracted outermembrane vesicle (DOC OMV) vaccine preparations from meningococcal strains Z1092 (A:4,21:P1.10), BZ198 (B:NT:P.1.4), and RM1090 (C:2a:P1.2), respectively.
• Lane 1 molecular mass standards.
• Lane 2 Z1092 MV.
• Lane 3 Z1092 DOC MV.
• Lane 4 Z 1092 OMV.
• FIG. 3 is a series of graphs showing binding of anti-CHORI vaccine, anti- Norwegian vaccine and control antisera and mAb to live encapsulated meningococcal B strains MC58 (B:15:P1.7,16) and S3446 (B:19,14:P1.23,14), as determined by indirect fluorescence flow cytometry. All antisera were tested at dilutions of 1 :20.
• the control mAb is an anti-capsule-specific murine mAB (Granoff et al., 1998, J. Immunol. 160: 5028-5036).
• the control antisera were pooled sera from mice immunized with proteins from the supernatant culture of E. coli strain BL21 or guinea pigs immunized with the adjuvant, aluminum hydroxide, alone.
• the strain MC58 has the same serotype and serosubtype as the strain used to prepare OMV for the Norwegian vaccine.
• the serotype and serosubtype of strain S3446 is heterologous to the strains used to prepare both vaccines.
• Figure 4 presents data regarding the bacterial cell surface binding of antisera determined by indirect fluorescence flow cytometry
• Figure 5 presents data illustrating the reactivity of CHORI antisera against N. meningitidis serogroup A and C strains.
• Figure 6 summarizes the results of a bactericidal assay testing anti-CHORI vaccine, anti-rNspA, and anti-Norwegian vaccine antisera against meningococcal B strain 2996.
• Figure 7 provides data showing the complement-mediated bactericidal activity of antisera and antibodies.
• Figure 8 provides data showing the complement-mediated bactericidal activity of antisera from mice immunized with the indicated vaccines.
• Figure 9 provides data showing the bactericidal activity of antisera from guinea pigs immunized with the indicated vaccines.
• Figure 10 provides data showing the passive protection in infant rats against meningococcal B strain 8047 bacteremia by antisera and antibodies.
• Figure 11 provides data showing the passive protection in infant rats against meningococcal B strain 8047 bacteremia by guinea pig antisera.
• Figure 12 is a photograph of a silver stained 15% SDS-PAGE gel of surface-exposed proteins precipitated by anti-CHORI antigen antisera from non-encapsulated meningococcal B strain M7. Lane 1, total protein from M7. Lane 2, proteins precipitated by murine anti- CHORI antisera. Lane 3, proteins precipitated by murine negative control antisera. The numbers on the left of the figure indicate apparent molecular mass in kDa.
• Figure 13 is a photograph of a Western blot of a 15% SDS-PAGE gel of surface- exposed proteins precipitated by anti-CHORI antigen antisera from non-encapsulated meningococcal B strain M7. Lanes 1 and 4, total protein from M7. Lanes 2 and 5, proteins precipitated by murine anti-CHORI antigen antisera. Lanes 3 and 6, proteins precipitated by murine negative control antisera.
• Anti-CHORI antigen antisera were used as the primary detecting antibody in lanes 1 to 3 and an anti-PorA mAb MN16C13F4 (Rijksinstituut Voor Herbstgezondeid en Mileu, Biltoven, The Netherlands) that is specific for serosubtype PI .2 was used as the primary detecting antibody in lanes 4 to 5.
• Figure 14 provides data showing the bacterial surface accessible proteins precipitated by pooled antisera from mice sequentially immunized with MenC strain RMI 090 MV, MenB strain BZ198 MV, and MenA strain Z1092 OMV.
• Figure 14A provides additional examples of data showing the bacterial surface accessible proteins precipiated by pooled anitsera from mice sequentially immunized with MenC strain RM1090 MV, MenB strain BZ198 MV, and MenA strain Z1092 OMV.
• Figure 15 is a photograph of a Western blot of a 15% SDS-PAGE gel of MV or OMV preparations.
• Primary detecting antisera is pooled mouse anti-CHORI/CFA vaccine antisera in lanes 1 to 3, pooled mouse anti-CHORI/ Al 2 (OPO 3 ) 3 in lanes 4 and 5, and pooled guinea pig anti-CHORI/Al 2 (OPO 3 )3 in lanes 6 to 8.
• Lanes 1 and 6 MV proteins prepared from strain RM1090.
• the numbers on the left of the figure indicate apparent molecular mass in kDa.
• Figure 16 provides data showing the apparent molecular masses of proteins from the indicated MN or OMV preparations that are reactive with antisera from mice and guinea pigs that were sequentially immunized with MN from MenC strain RMI 090 and MenB strain BZ198, and OMN from MenA strain Z1092.
• Figure 17 provides data from ELISA showing the absorption of anti-LOS antibodies from pooled antisera obtained from mice and guinea pigs sequentially immunized with MV from MenC strain RM1090 and MenB strain BZ198, and OMV from MenA strain Z1092, or three injections of a mixture of the three vesicle preparations.
• Figure 18 provides data from complement-mediated bactericidal assay showing that the absorption of anti-LOS antibodies from pooled antisera obtained from mice and guinea pigs sequentially immunized with MV from MenC strain RMI 090 and MenB strain BZ198, and OMV from MenA strain Z1092, or three injections of a mixture of the three vesicle preparations does not significantly change the bactericidal activity of the antisera against MenB strains that are homologous or heterologous to the vaccine strains.
• Figure 19 provides data from a whole cell ELISA showing examples of mAbs produced from mice sequentially immunized with MV from MenC strain RMI 090 and MenB strain BZ198, and OMV from MenA strain Z1092.
• Figure 20 summarizes the complement-mediated bactericidal activity of mAbs prepared from mice immunized with anti-CHORI antigen and tested against several MenB strains.
• Figure 21 summarizes the meningococcal serotype and serosubtype defining monoclonal antibodies available from RIVM
• Figure 22 summarizes the serogroup, serotype, and serosubtype defining monoclonal antibodies available from NDBSC
• dates of publication provided may be different from the actual publication dates which may need to be independently confirmed.
• OMV meningococcal outer membrane vesicle
• the serum bactericidal antibody response to OMV vaccines tends to be strain specific (Tappero et al., 1999, JAMA 281 : 1520; and Rouupe van der Voort ER, 2000, Vaccine, 18:1334-1343).
• PorA is immunodominant, and the immunity induced is predominantly specific to the strains from which the membrane vesicles were obtained (Tappero et al., 1999, JAMA 281:1520; Martin SL et al, 2000, Vaccine, 18:2476-2481). This limitation is primarily because of antigenic variability of the PorA protein and is particularly true in infants who are immunologically naive (Tappero et al.) with respect to prior exposure to neisserial antigens.
• the present invention involves eliciting an immune response that is broadly reactive with diverse disease-producing N. meningitidis strains.
• the invention circumvents the problem of immunodominance of antigenically variable domains of PorA in vesicle-or PorA-based vaccines by focusing the antibody response on common antigens in the vaccine strains.
• the methods of the invention elicit serum bactericidal antibody, the only proven serologic correlate of protection in humans (Goldschneider et al. 1969, supra), against strains of Neisseria expressing serosubtype epitopes that were not used in the vaccine preparations.
• the method elicits serum bactericidal antibody against strains that are not killed by antibody to a conserved protein such as Neisserial surface protein A, a candidate meningococcal vaccine (Martin et al., 2000. J. Biotechnol. 83:27-31; Moe et al. (1999 Infect. Immun. 67: 5664; Moe et al. Infect Immun. 2001 69:3762).
• a conserved protein such as Neisserial surface protein A
• Moe et al. (1999 Infect. Immun. 67: 5664; Moe et al. Infect Immun. 2001 69:3762 elicits serum bactericidal antibody against strains that are not killed by antibody to a conserved protein such as Neisserial surface protein A, a candidate meningococcal vaccine (Martin et al., 2000. J. Biotechnol. 83:27-31; Moe et al. (1999 Infect. Immun. 67: 5664;
• protective immunity means that a vaccine or immunization schedule that is administered to a mammal induces an immune response that prevents, retards the development of, or reduces the severity of a disease that is caused by Neisseria me? ⁇ ingitidis, or diminishes or altogether eliminates the symptoms of the disease.
• a disease caused by a strain of serogroup B of Neisseria meningitidis encompasses any clinical symptom or combination of clinical symptoms that are present in an infection with a member of serogroup B of Neisseria meningitidis. These symptoms include but are not limited to: colonization of the upper respiratory tract (e.g.
• mucosa of the nasopharynx and tonsils by a pathogenic strain of serogroup B of Neisseria meningitidis, penetration of the bacteria into the mucosa and the submucosal vascular bed, septicemia, septic shock, inflammation, haemmorrhagic skin lesions, activation of fibrinolysis and of blood coagulation, organ dysfunction such as kidney, lung, and cardiac failure, adrenal hemorrhaging and muscular infarction, capillary leakage, edema, peripheral limb ischaemia, respiratory distress syndrome, pericarditis and meningitis.
• the phrase "broad spectrum protective immunity” means that a vaccine or immunization schedule elicits "protective immunity” against at least one or more (or against at least two, at least three, at least four, at least five, against at least eight, or at least against more than eight) strains of Neisseria meningitidis, wherein each of the strains belongs to a different serosubtype as the strains used to prepare the vaccine.
• the invention specifically contemplates and encompasses a vaccine or vaccination regimen that confers protection against a disease caused by a member of serogroup B of Neisseria meningitidis and also against other serogroups, particularly serogroups A, C, Y and W-135.
• an antigen such as a polysaccharide, phospholipid, protein or peptide
• the specified antibody or antibodies bind(s) to a particular antigen or antigens in a sample and do not bind in a significant amount to other molecules present in the sample.
• Specific binding to an antibody under such conditions may require an antibody or antiserum that is selected for its specificity for a particular antigen or antigens.
• Immune response indicators include but are not limited to: antibody titer or specificity, as detected by an assay such as enzyme-linked immunoassay (ELIS A), bactericidal assay, flow cytometry, immunoprecipitation, Ouchter-Lowny immunodifrusion; binding detection assays of, for example, spot, Western blot or antigen arrays; cytotoxicity assays, etc.
• a "surface antigen” is an antigen that is present in a surface structure of Neisseria meningitidis (e.g. the outer membrane, inner membrane, periplasmic space, capsule, pili, etc.).
• genetically diverse refers to strains that differ from one another in the amino acid sequence of at least one, and usually at least two, more usually at least three polypeptides, particularly antigenic polypeptides. Genetic diversity of strains can be accomplished by selecting strains that differ in at least one or more, preferably at least two or more, of serogroup, serotype, or serosubtype (e.g., two strains that differ in at least one of the proteins selected from outer membrane, PorA and PorB proteins, are said to genetically diverse with respect to one another).
• Genetic diversity can also be defined by, for example, multi-locus sequence typing and/or multi-locus enzyme typing (see, e.g., Maiden et al., 1998, Proc. Natl. Acad Sci. USA 95:3140; Pizza et al. 2000 Science287:1816), multi-locus enzyme electrophoresis, and other methods known in the art.
• "Serogroup” as used herein refers to classification of Neisseria meningitides by virtue of immunologically detectable variations in the capsular polysaccharide. About 12 serogroups are known: A, B, C, X, Y, Z, 29-E, W-135, H, I, K and L.
• serogroup can encompass multiple serotypes and multiple serosubtypes.
• serotype refers to classification of Neisseria meningitides strains based on monoclonal antibody defined antigenic differences in the outer membrane protein Porin B. A single serotype can be found in multiple serogroups and multiple serosubtypes.
• serosubtype refers classification of Neisseria meningitides strains based on antibody defined antigenic variations on an outer membrane protein called Porin A, or upon VR typing of amino acid sequences deduced from DNA sequencing (Sacchi et al., 2000, J. Infect. Dis. 182: 1169; see also the Multi Locus Sequence Typing web site).
• PorA proteins Most variability between PorA proteins occurs in two (loops I and IV) of eight putative, surface exposed loops.
• the variable loops I and IV have been designated VRl and VR2, respectively.
• a single serosubtype can be found in multiple serogroups and multiple serotypes.
• Enriched means that an antigen in an antigen composition is manipulated by an experimentalist or a clinician so that it is present in at least a three-fold greater concentration by total weight, preferably at least 10-fold greater concentration, more preferably at least 100-fold greater concentration, and most preferably at least 1, 000-fold greater concentration than the concentration of that antigen in the strain from which the antigen composition was obtained.
• concentration of a particular antigen is 1 microgram per gram of total bacterial preparation (or of total bacterial protein)
• an enriched preparation would contain at least 3 micrograms per gram of total bacterial preparation (or of total bacterial protein).
• Neisseria meningitidis denotes an individual (e.g., a mammal such as a human patient) that has never been exposed (through infection or administration) to Neisseria meningitidis or to an antigen composition derived from Neisseria meningitidis in sufficient amounts to elicit protective immunity, or if exposed, failed to mount a protective immune response. (An example of the latter would be an individual exposed at a too young age when protective immune responses may not occur. Molages et al., 1994, Infect. Immun. 62: 4419-4424).
• the "immunologically na ⁇ ve" individual has also not been exposed to a Neisserial species other than Neisseria meningitidis (or an antigen composition prepared from a Neisserial species), particularly not to a cross-reacting strain of Neisserial species (or antigen composition). Individuals that have been exposed (through infection or administration) to a Neisserial species or to an antigen composition derived from that
• the various antigenic compositions e.g. lysed cells, subcellular fractions, MNs and OMVs, or individual antigens and combinations of antigens detected and isolated as described above and below
• an animal especially a human patient
• the antigen preparations used to elicit an immune response are prepared by culturing Neisseria meningitidis spp. using well-known bacterial culture techniques and preparing a fraction that contains antigens that induce protective immunity.
• MNs may be obtained by culturing a strain of Neisseria meningitidis in broth culture medium, separating whole cells from the broth culture medium (e.g. by filtration, or by a low-speed centrifugation that pellets only the cells and not the smaller blebs, or the like), and then collecting the MNs that are present in the cell-free culture medium (e.g. by filtration, differential precipitation or aggregation of MVs, or by a high-speed centrifugation that pellets the blebs, or the like).
• Strains for use in production of MNs can generally be selected on the basis of the amount of blebs produced in culture (e.g., bacteria can be cultured in a reasonable number to provide for production of blebs suitable for isolation and administration in the methods described herein).
• An exemplary strain that produces high levels of blebs is described in PCT Publication No. WO 01/34642.
• strains for use in MV production may also be selected on the basis of NspA production, where strains that produce higher levels of NspA may be preferable (for examples of N. meningitides strains having different NspA production levels, see, e.g., Moe et al. (1999 Infect. Immun. 67: 5664).
• a second preferred fraction comprises outer membrane vesicles (OMV) prepared from the outer membrane of a cultured strain of Neisseria meningitidis spp.
• OMNs may be obtained from a Neisseria meningitidis grown in broth or solid medium culture, preferably by separating the bacterial cells from the culture medium (e.g. by filtration or by a low-speed centrifugation that pellets the cells, or the like), lysing the cells (e.g. by addition of detergent, osmotic shock, sonication, cavitation, homogenization, or the like) and separating an outer membrane fraction from cytoplasmic molecules (e.g.
• outer membrane fractions may be used to produce OMNs.
• MNs or OMNs it may be preferable to use strains that are relatively low producers of endotoxin (lipopolysaccharide, LPS) so as to decrease the need to remove endotoxin from the final preparation prior to use in humans.
• LPS lipopolysaccharide
• the OMN and/or MN can be prepared from mutants of these Neisseria strains in which lipooligosaccharide or other antigens that may be undesirable in a vaccine (e.g. Rmp) is reduced or eliminated.
• a vaccine e.g. Rmp
• the MVs or OMVs are optionally treated to reduce endotoxin, e.g., to reduce toxicity following administration.
• Reduction of endotoxin can be accomplished by extraction with a suitable detergent (for example, BRIJ- 96, sodium deoxycholate, sodium lauoylsarcosinate, Empigen BB, Triton X- 100, TWEEN 20 (sorbitan monolaurate polyoxyethylene), TWEEN 80, at a concentration of 0.1-10%, preferably 0.5-2%).
• a suitable detergent for example, BRIJ- 96, sodium deoxycholate, sodium lauoylsarcosinate, Empigen BB, Triton X- 100, TWEEN 20 (sorbitan monolaurate polyoxyethylene), TWEEN 80, at a concentration of 0.1-10%, preferably 0.5-2%.
• a detergent other than deoxycholate Extraction of OMV and MN preparations with deoxycholate resulted in removal of some non-capsular protein antigens (see Figure 2). Vaccination of animals with OMV or MV preparations subjected to deoxycholate extraction elicit
• Immunogenic compositions used as vaccines comprise an immunologically effective amount of antigen, as well as any other compatible components, as needed.
• immunologically effective amount is meant that the administration of that amount to an individual, either in a single dose or as part of a series, is effective for treatment or prevention.
• Dosage treatment may be a single dose schedule or a multiple dose schedule (e.g., including booster doses).
• the vaccine may be administered in conjunction with other immunoregulatory agents.
• the antigen compositions or individual antigens to be administered are provided in a pharmaceutically acceptable solution such as an aqueous solution, often a saline solution, or they can be provided in powder form.
• the compositions may also include an adjuvant.
• suitable adjuvants that can be used in humans include, but are not necessarily limited to, alum, aluminum phosphate, aluminum hydroxide, MF59 (4.3% w/v squalene, 0.5% w/v Tween 80, 0.5% w/v Span 85), CpG-containing nucleic acid (where the cytosine is unmethylated), QS21, MPL, 3DMPL, extracts from Aquilla, ISCOMS, LT/CT mutants, poly(D,L-lactide-co-glycolide) (PLG) microparticles, Quil A, interleukins, and the like.
• thr-MDP N-acetyl-muramyl-L-threonyl-D- isoglutamine
• CGP 11637 N-acetyl-nor-muramyl-L-alanyl-D-isoglutamine
• nor-MDP N-acetylmuramyl-L-alanyl-D-isoglutaminyl-L-alanine-2-( -2'- dipalmitoyl-sn-glycero-3-hydroxyphosphoryloxy)-ethylamine
• P BI which contains three components extracted from bacteria, monophosphoryl lipid A, trehalose dimycolate and cell wall skeleton (MPL+TDM+CWS) in a 2% squalene/Tween 80 emulsion.
• the effectiveness of an adjuvant may be determined by measuring the amount of antibodies directed against the immuno
• adjuvants to enhance effectiveness of thecomposition include, but are not limited to: (1) oil-in-water emulsion formulations (with or without other specific immunostimulating agents such as muramyl peptides (see below) or bacterial cell wall components), such as for example (a) MF59TM (W090/14837; Chapter 10 in Vaccine design: the subunit and adjuvant approach, eds.
• cytokines such as interleukins (e.g. IL-1, IL-2, IL-4, IL-5, IL-6, JL-7, IL-12 (WO99/44636), etc.), interferons (e.g. gamma interferon), macrophage colony stimulating factor (M-CSF), tumor necrosis factor (TNF), etc.; (5) monophosphoryl lipid A (MPL) or 3-O-deacylated MPL (3dMPL) e.g.
• MPL monophosphoryl lipid A
• 3dMPL 3-O-deacylated MPL
• GB-2220221, EP-A-0689454 optionally in the substantial absence of alum when used with pneumococcal saccharides e.g. WO00/56358; (6) combinations of 3dMPL with, for example, QS21 and/oroil-in-water emulsions e.g.
• WO98/55495, WO98/37919 and WO98/52581] i.e. containing at least one CG dinucleotide, where the cytosine is unmethylated; (8) a polyoxyethylene ether or a polyoxyethylene ester e.g. WO99/52549; (9) a polyoxyethylene sorbitan ester surfactant in combination with an octoxynol (WOO 1/21207) or a polyoxyethylene alkyl ether or ester surfactant in combination with at least one additional non-ionic surfactant such as an octoxynol (WOOl/21152); (10) a saponin and an immunostimulatory oligonucleotide (e.g.
• a CpG oligonucleotide (WO00/62800); (11) an immunostimulant and a particle of metal salt e.g. WO00/23105; (12) a saponin and an oil-in-water emulsion e.g. WO99/11241; (13) a saponin (e.g. QS21) + 3dMPL + IM2 (optionally + a sterol) e.g. WO98/57659; (14) other substances that act as immunostimulating agents to enhance the efficacy of the composition.
• Muramyl peptides include N-acetyl-muramyl-L-threonyl-D- isoglutarnine (thr-MDP), N-25 acelyl-normuramyl-L-alanyl-D-isoglutamine (nor-MDP), N- acetylmuramyl-llr-alanyl-D-isoglutaminyl-I ⁇ alanh hydroxyphosphoryloxy)-emylarnine MTP-PE), etc.
• the antigens may be combined with conventional excipients, such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharin, talcum, cellulose, glucose, sucrose, magnesium, carbonate, and the like.
• the compositions may contain pharmaceutically acceptable auxiliary substances as required to approximate physiological conditions such as pH adjusting and buffering agents, toxicity adjusting agents and the like, for example, sodium acetate, sodium chloride, potassium chloride, calcium chloride, sodium lactate and the like.
• the concentration of antigen in these formulations can vary widely, and will be selected primarily based on fluid volumes, viscosities, body weight and the like in accordance with the particular mode of administration selected and the patient's needs.
• the resulting compositions may be in the form of a solution, suspension, tablet, pill, capsule, powder, gel, cream, lotion, ointment, aerosol or the like.
• the concentration of immunogenic antigens of the invention in the pharmaceutical formulations can vary widely, i.e. from less than about 0.1%, usually at or at least about 2% to as much as 20% to 50% or more by weight, and will be selected primarily by fluid volumes, viscosities, etc., in accordance with the particular mode of administration selected.
• the MVs, OMVs, isolated antigens, or combinations of antigens of the present invention are administered orally, nasally, nasopharyngeally, parenterally, enterically, gastrically, topically, transdermally, subcutaneously, intramuscularly, in tablet, solid, powdered, liquid, aerosol form, locally or systemically, with or without added excipients.
• parenterally administrable compositions will be known or apparent to those skilled in the art and are described in more detail in such publications as Remington's Pharmaceutical Science, 15th ed., Mack Publishing Company, Easton, Pennsylvania (1980).
• Administration of the MVs, OMVs, isolated antigens, or combinations of antigens can be performed serially or as a mixture, as described in more detail below.
• polypeptides and related compounds described above when administered orally, must be protected from digestion. This is typically accomplished either by complexing the protein with a composition to render it resistant to acidic and enzymatic hydrolysis or by packaging the protein in an appropriately resistant carrier such as a liposome. Means of protecting proteins from digestion are well known in the art.
• the antigenic preparations that are injected may also be encapsulated, introduced into the lumen of liposomes, prepared as a colloid, or other conventional techniques may be employed which provide an extended serum half-life of the peptides.
• liposomes A variety of methods are available for preparing liposomes, as described in, e.g., Szoka et al., Ann. Rev. Biophys. Bioeng. 9:467 (1980), U.S. Patents Nos. 4, 235,871, 4,501,728 and 4,837,028.
• the preparations may also be provided in controlled release or slow-release forms for release and administration of the antigen preparations as a mixture or in serial fashion.
• compositions are administered to an animal that is at risk from acquiring a Neisserial disease to prevent or at least partially arrest the development of disease and its complications.
• An amount adequate to accomplish this is defined as a "therapeutically effective dose.” Amounts effective for therapeutic use will depend on, e.g., the antigen composition, the manner of administration, the weight and general state of health of the patient, and the judgment of the prescribing physician. Single or multiple doses of the antigen compositions may be administered depending on the dosage and frequency required and tolerated by the patient, and route of administration.
• the antigen compositions described herein are administered serially.
• a therapeutically effective dose of a first antigen composition e.g. MV, OMV, isolated antigen, or combinations of antigens, with or without excipients
• the first antigenic composition is generally administered in an amount effective to elicit a immune response (e.g., activation of B and/or T cells).
• Amounts for the initial immunization generally range from about 0.001 mg to about 1.0 mg per 70 kilogram patient, more commonly from about 0.001 mg to about 0.2 mg per 70 kilogram patient.
• Dosages from 0.001 up to about 10 mg per patient per day may be used, particularly when the antigen is administered to a secluded site and not into the blood stream, such as into a body cavity or into a lumen of an organ. Substantially higher dosages (e.g. 10 to 100 mg or more) are possible in oral, nasal, or topical administration.
• a therapeutically effective dose of a second antigen composition (e.g. MN, OMN, isolated antigen, or combinations of antigens, with or without excipients) prepared from a second Neisserial strain is administered to an individual after the individual has been immunologically primed by exposure to the first antigen composition.
• the booster may be administered days, weeks or months after the initial immunization, depending upon the patient's response and condition.
• the existence of an immune response to the first antigen composition may be determined by known methods (e.g.
• Immunologic priming and/or the existence of an immune response to the first antigen composition may also be assumed by waiting for a period of time after the first immunization that, based on previous experience, is a sufficient time for an immune response and/or priming to have taken place — e.g. 2, 4, 6, 10 or 14 weeks.
• Boosting dosages of the second antigen composition are typically from about 0.001 mg to about 1.0 mg of antigen, depending on the nature of the immunogen and route of immunization.
• a therapeutically effective dose of a third antigen composition prepared from a third Neisserial strain is administered to an individual after the individual has been primed and/or mounted an immune response to the second antigen composition.
• the third booster may be administered days, weeks or months after the second immunization, depending upon the patient's response and condition.
• the existence of priming and/or an immune response to the second antigen composition may be determined by the same methods used to detect an immune response to the second antigen composition.
• the existence of priming and/or an immune response to the second antigen composition may also be assumed by waiting for a period of time after the second immunization that, based on previous experience, is a sufficient time for an immune response to have taken place — e.g. 2, 4, 6, 10 or 14 weeks.
• Boosting dosages of the second antigen composition are typically from about 0.001 mg to about 1.0 mg of antigen, depending on the nature of the immunogen and route of immunization.
• the present invention further contemplates the use of a fourth, fifth, sixth or greater booster immunization, using either a fourth, fifth or sixth strain of Neisseria meningitidis or any of the first, second, or third strains, or other strain that is genetically diverse with respect to at least one of the first, second, and third strains.
• admimstration of antigenic compositions prepared from the first, second, and (optionally, but preferably) third strains is serial, the order of administration of the compositions can be varied.
• the order of administration of OMV and/or MV within these serial administration steps can be varied.
• the following orders of administration are within the scope of the invention (from left to right, with the third administration being optional): OMV-OMV-OMV; OMV-OMV-MV; OMV-MV-MV; MV- MV-MV; MV-MV-OMV; MN-OMN-OMN; OMV-MV-OMV; and MV-OMV-MV.
• the order of administration is MV-MV-OMV.
• first, second, and (optionally) third antigen compositions are administered as a mixture.
• first and second antigen compositions are administered as a mixture, and the third antigen composition is administered subsequently.
• the mixtures is administered in an amount effective to elicit an immune response, particularly a humoral immune response, in the host.
• Amounts for the immunization of the mixture generally range from about 0.001 mg to about 1.0 mg per 70 kilogram patient, more commonly from about 0.001 mg to about 0.2 mg per 70 kilogram patient. Dosages from 0.001 up to about 10 mg per patient per day may be used, particularly when the antigen is administered to a secluded site and not into the blood stream, such as into a body cavity or into a lumen of an organ. Substantially higher dosages (e.g. 10 to 100 mg or more) are possible in oral, nasal, or topical administration.
• the initial administration of the mixture can be followed by booster immunization of the same of different mixture, with at least one booster, more usually two boosters, being preferred.
• the first and second Neisserial strains are genetically diverse to one another, e.g., the strains belong to different PorB serotypes and/or PorA serosubtypes; and may also optionally belong to different capsular serogroups.
• the second and third Neisserial strains are genetically diverse to one antoher, e.g., the strains belong to different serotypes and/or serosubtypes; may also optionally belong to different serogroups.
• the third Neisserial strain is preferably genetically diverse with respect to the first and second strains, but may, in some embodiments, not be genetically diverse with respect to the first strain.
• the serotype and/or serosubtype of the third Neisserial strain should preferably be different from the first and second strain but it may be the same as the first strain.
• the present invention also specifically contemplates that antigen compositions from other members of the genus Neisseria may be administered as described herein to generate protective immunity against Neisseria meningitidis.
• Neisseria lactamica a nonpathogenic non-encapsulated commensal member of the genus Neisseria that is commonly found in the human nasopharynx, encompasses strains which have many antigens present on N. meningitidis and, therefore, also may be used to prepare one of the immunogens envisioned in this invention.
• MNs and OMNs from the nonpathogenic Neisseria lactamica may be used to prime or elicit a protective immune response against Neisseria meningitidis (or against other pathogenic Neisseria such as Neisseria gonorrhea).
• an antigen composition e.g., MN or OMV
• Neisseria lactamica an antigen composition from Neisseria lactamica
• a second and optionally a third antigen composition from Neisseria meningitidis or Neisseria gonorrhea
• the invention specifically contemplates also that antigen compositions from Neisseria lactamica strains be used for the initial, second and any subsequent administrations, wherein each lactamica strain has a different serotype and/or serosubtype as the others.
• the antigen compositions used at any step in the immunization protocol may be obtained from one or more strains of bacteria (especially Neisseria lactamica or Neisseria meningitidis) that are genetically engineered by known methods (see, e.g. U.S. Pat. No. 6,013,267) to express one or more nucleic acids that encode one or more molecules of interest, particularly molecules that elicit or enhance a protective immune response.
• the nucleic acids may, for example, encode Porin A, Porin B, NspA, pilin, or other Neisserial proteins.
• nucleic acids include those that encode Neisserial proteins immunoprecipitated with anti-sera produced following vaccination with the CHORI vaccine, particularly those proteins having apparent molecular masses of about 80 kDa, about 59.5 kDa, about 40.7 kDa. about 39.6 kDa, about 33 kDa, about 27.9 kDa, and 14.5 kDa, or antigenic fragments thereof.
• nucleic acids include those that encode Neisserial proteins detected by Western blot with anti-sera produced following vaccination with the CHORI vaccine, particularly those proteins having apparent molecular masses of about 53 kDa-57 kDa; about 46-47 kDa, about 33 kDa, about 20 kDa to 21 kDa; and about 18 kDa.
• the nucleic acids may encode any of the above proteins that is truncated, or altered to include or delete a glycosylation site, or to include or delete any epitope, or to increase the expression of any of the above proteins. Of particular interest are antigenic fragments of such proteins.
• the antigen compositions of the invention can comprise additional antigens of N.
• meningiditis such as those exemplified in PCT Publication Nos. WO 99/24578, WO 99/36544; WO 99/57280, WO 00/22430, and WO 00/66791, as well as antigenic fragments of such proteins.
• the antigen compositions used to prime and boost a broad protective immunity against Neisseria meningitidis are prepared from strains of Neisseria that possess variant immunodominant antigens (the main antigens that are routinely detected by antisera from different host animals that have been infected with Neisseria; representative examples include Porin A, Porin B, pilin, NspA etc.).
• the strains vary with respect to either PorA or PorB, as evinced by their serotype or serosubtype.
• the strains also may vary with respect to the capsule molecule, as reflected by their serogroup.
• Serotype and serosubtype classification is currently determined by detecting which of a panel of known monoclonals, which are known to recognize specific Porin molecules, bind to an unknown strain (Sacchi et al., 1998, Clin. Diag. Lab. Immunol. 5:348, see Tables 8 and 9 for partial lists of monoclonals). It is probable that other such monoclonals will be identified.
• the use of any novel serotypes and serosubtypes which may be defined by any new monoclonals are specifically contemplated by the invention.
• serotypes and serosubtypes may be defined, not only by interaction with monoclonal antibodies, but also structurally by the absence and/or presence of defined peptide residues and peptide epitopes (Sacchi et al., 2000, J. Infect. Dis. 182: 1169). Serotype and serosubtype classification schemes that are based on structural features of the Porins (known or that may be discovered at a later date) are specifically encompassed by the invention.
• One purpose and effect of serial administration of antigen compositions from different strains is to potentiate an immune response to antigens and epitopes that are typically not immunodominant, particularly non-immunodominant epitopes that exhibit less genetic variability than the known immunodominant epitopes.
• the invention specifically encompasses the serial administration of antigen compositions from Neisserial strains that differ with respect to immunodominant antigens other than the Porins (e.g., phospholipids, polysaccharides, lipopolysaccharides, pilins, OmpA, Opa, Ope, etc.).
• the antigen compositions are typically administered to a mammal that is immunologically na ⁇ ve with respect to Neisseria meningitidis.
• the mammal is a human child about five years or younger, and preferably about two years old or younger, and the antigen compositions are administered at any one or more of the following times: two weeks, one month, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11 months, or one year or 15, 18, or 21 months after birth, or at 2, 3, 4, or 5 years of age.
• administration to any mammal is preferably initiated prior to the first sign of disease symptoms, or at the first sign of possible or actual exposure to Neisseria.
• these antigens may be directly administered instead of MVs or OMVs.
• the DNA encoding one or more of the peptides of the invention can also be administered to the patient. This approach is described, for instance, in Wolff et al., Science 247: 1465-1468 (1990), as well as U.S. Patents Nos. 5,580,859 and 5,589,466.
• Subcellular fractions such as MVs and OMVs contain many antigens that may give rise to an immune response (see, e.g., Figure 2 which depicts an electrophoretic gel of several such fractions).
• the present invention also relates to individual antigens and/or combinations of antigens that induce protective immunity. Another objective is to use the identified antigens to formulate antigen compositions that may be used to elicit protective immunity against a Neisserial disease.
• Antisera or mAbs are obtained or produced from mammals that are induced by the methods of the present invention to exhibit protective immunity against a disease caused by a Neisseria meningitidis spp..
• the antisera or mAbs are used to detect their corresponding Neisserial antigens, and the these antigens identified and isolated based on their physicochemical properties (class of molecule: peptide, nucleic acid, etc.; molecular mass, charge, chemical composition, etc.) or amino acid sequence.
• the isolated antigens (or immunologically effective portions thereof) can then be administered to mammals, singly and/or in combination, as described above, or as recombinant proteins (or immunologically effective fragments thereof) to assess the extent to which they induce protective immunity.
• the present invention specifically contemplates serially administering antigens isolated from one strain or different strains of Neisseria, or administering such antigens in a mixture comprising one or more, usually two or more, more usually three or more, still more usually four to six or more antigens.
• Exemplary Neisserial antigens suitable for administration as described may include, but are not necessarily limited to those proteins immunoprecipitated with anti-sera produced following vaccination with the CHORI vaccine, particularly those proteins having apparent molecular masses of about 80 kDa, about 59.5 kDa, about 40.7 kDa. about 39.6 kDa, about 33 kDa, about 27.9 kDa, and 14.5 kDa, or antigenic fragments thereof.
• the antigens administered may include at least one of these antigens, or may include a combination of these antigens (e.g., at least two, at least three, at least four, or more).
• Neisserial antigens suitable for administration as described may include, but are not necessarily limited to those proteins detected by Western blot with anti- sera produced following vaccination with the CHORI vaccine, particularly those proteins having apparent molecular masses of about 53 kDa-57 kDa; about 46-47 kDa, about 33 kDa, about 20 kDa to 21 kDa; and about 18 kDa, or antigenic fragments thereof.
• the antigens administered may include at least one of these antigens, or may include a combination of these antigens (e.g., at least two, at least three, at least four, or more).
• references made to molecular masses of proteins refer to apparent molecular mass as determined using SDS-PAGE under the conditions described. It will be readily apparent to the ordinarily skilled artisan upon reading the present specification that these apparent molecular masses may vary for the same protein between two different experiments (e.g., using different gels or different preparations, when isolated from two different strains (e.g., due to polymorphisms between strains due to amino acid substitutions, deletions, and/or insertions, post-translational modifications, and the like)), and further that different proteins may appear to have the same apparent molecular mass.
• Antigens that elicit protective immunity are detected by known methods: for example, immunoassay, immunoprecipitation, affinity chromatography, Western blots, etc. Examples of such methods are described below.
• the first step is generally producing antiserum or an antibody preparation that binds to the antigen or antigenic composition.
• the animal's immune response to the immunogen preparation is monitored by taking test bleeds and determining the titer of reactivity of serially diluted aliquots of serum to serially diluted aliquots of the antigenic composition.
• Polyclonal antisera with a titer of 10 4 or greater are selected and tested for their cross reactivity against non-immunogenic controls, using a competitive binding immunoassay.
• Specific monoclonal and polyclonal antibodies and antisera will usually bind with a dissociation constant (K D ) of at least about 0.1 mM, more usually at least about 1 ⁇ M, preferably at least about 0.1 ⁇ M or better, and most preferably, .01 ⁇ M or better.
• K D dissociation constant
• monoclonal antibodies from various mammalian hosts, such as mice, rodents, primates, humans, etc.
• Description of techniques for preparing such monoclonal antibodies are found in, e.g., Stites et al. Supra, and references cited therein; Harlow and Lane, Supra; Goding Supra; and Kohler and Milstein. Supra. Summarized briefly, this method proceeds by injecting an animal with an immunogenic preparation. The animal is then sacrificed and cells taken from its spleen, which are fused with myeloma cells. The result is a hybrid cell or "hybridoma" that is capable of reproducing in vitro.
• the population of hybridomas is then screened to isolate individual clones, each of which secrete a single antibody species to the immunogen.
• the individual antibody species obtained are the products of immortalized and cloned single B cells from the immune animal generated in response to a specific site recognized on the immunogenic substance.
• an immune serum or a monoclonal antibody that recognizes one or more Neisserial antigens may be used to perform immunoassays.
• immunoassays For a review of immunological and immunoassay procedures in general, see D. Stites and A. Terr, (eds.), Supra.
• the immunoassays of the present invention can be performed in any of several configurations, which are reviewed extensively in ENZYME IMMUNOASSAY, E.T. Maggio, ed., CRC Press, Boca Raton, Florida (1980); "Practice and Theory of Enzyme Immunoassays," P.
• solid-phase ELISA immunoassays are routinely used to select monoclonal antibodies specifically immunoreactive with an antigen. See Harlow and Lane, Supra. Immunoabsorbed and/or pooled antisera (or monoclonal antibodies) are also used in a direct or competitive binding immunoassay. The latter compares the binding of a second antigen composition (e.g. MVs, OMVs, isolated antigens or antigen compositions from an unknown or a known different Neisserial strain) to that of the reference antigen composition used to elicit protective immunity.
• a second antigen composition e.g. MVs, OMVs, isolated antigens or antigen compositions from an unknown or a known different Neisserial strain
• the two antigen preparations are each assayed at a wide range of concentrations and the amount of each molecule required to inhibit 50% of the binding of the antisera to the immobilized reference antigen preparation is determined. If the amount of the second protein required is less than 10 times the amount of the reference peptide used to make the antibody, then the second protein is said to specifically bind to an antibody generated to the reference antigen preparation.
• Western blot analysis generally comprises separating sample products by gel electrophoresis on the basis of molecular weight, transferring the separated proteins to a suitable solid support (such as a nitrocellulose filter, a nylon filter, or derivatized nylon filter), and incubating the sample with labeling antibodies that specifically bind to the analyte protein.
• the labeling antibodies specifically bind to analyte on the solid support.
• labeling agents such as antibodies (e.g. labeled sheep anti-mouse antibodies where the antibody to an analyte is a murine antibody) that specifically bind to the labeling antibody.
• the antigens can be isolated (separated from one or more molecules with which the antigen is associated in vivo) and purified (a purified antigen, e.g. a protein, preferably exhibits essentially a single band on an electrophoretic gel for each dissociable subunit of the antigen) and used to elicit protective immunity.
• a purified antigen e.g. a protein, preferably exhibits essentially a single band on an electrophoretic gel for each dissociable subunit of the antigen
• antigens can be purified by any of a variety of known techniques, including, for example, reverse phase high-performance liquid chromatography (HPLC), ion-exchange or immunoaffinity chromatography, separation by size, or electrophoresis (see, generally, Scopes, R. Protein Purification, Springer-Nerlag, ⁇ .Y. (1982)).
• HPLC reverse phase high-performance liquid chromatography
• ion-exchange or immunoaffinity chromatography separation by size
• electrophoresis see, generally, Scopes, R. Protein Purification, Springer-Nerlag, ⁇ .Y. (1982)
• antigens from Neisseria meningitidis spp. that are recognized by broad spectrum antisera obtained after serial injections of OMNs and/or MVs obtained from different Neisseria meningitidis spp. are obtained by using broad spectrum antisera to generate enriched antigen preparations.
• Isolated antigens may also be prepared by immunoprecipitating a fraction obtained from Neisseria meningitidis spp.
• the antigens may also be isolated by conjugating immune antisera or monoclonal antibodies to a column and performing affinity chromatography.
• the source of the antigens may be a whole cell lysate obtained by known methods, for example by sonication, or alternatively by exposure to an ionic or nonionic detergent, or the source may be MVs or OMNs from a Neisserial strain.
• antigen preparations from Neisseria meningitidis spp. suitable for inducing protective immunity in the present invention can be generated by synthesizing peptides by conventional techniques, and injecting synthetic peptide preparations into a mammal.
• Techniques for peptide synthesis are well known in the art. See, e.g., Stewart and Young, Solid Phase Peptide Synthesis (Rockford, 111., Pierce), 2d Ed. (1984) and Kent, 1988, Annu. Rev. Biochem. 57:957.
• nucleic acid sequences which encode the particular polypeptide may be cloned and expressed to provide the peptide.
• Standard techniques can be used to obtain and screen nucleic acid libraries to identify sequences encoding the desired sequences (see Sambrook et al., Molecular Cloning - A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, 1989), or nucleic acids that encode desired peptides may be synthesized by known methods. Fusion proteins (those consisting of all or part of the amino acid sequences of two or more proteins) can be recombinantly produced.
• unrelated proteins can be mutated to comprise the appropriate sequences.
• the immunogenic antigens of the present invention may be modified to provide a variety of desired attributes, e.g. improved pharmacological characteristics, while increasing or at least retaining substantially all of the biological activity of the unmodified peptide.
• the peptides can be modified by extending, decreasing the amino acid sequence of the peptide. Substitutions with different amino acids or amino acid mimetics can also be made.
• the peptides employed in the subject invention need not be identical to those disclosed in the Examples section below (e.g., with respect to molecular weight), so long as the subject peptides are able to induce an immune response against the desired antigen molecule.
• a number of conservative substitutions can be made without substantially affecting the activity of the peptide.
• Single amino acid substitutions, deletions, or insertions can be used to determine which residues are relatively insensitive to modification. Substitutions are preferably made with small, relatively neutral moieties such as Ala, Gly, Pro, or similar residues. The effect of single amino acid substitutions may also be probed using D-amino acids. The numbers and types of residues which are substituted or added depend on the spacing necessary between essential contact points and certain functional attributes which are sought (e.g. hydrophobicity versus hydrophilicity). Increased immunogenicity may also be achieved by such substitutions, compared to the parent peptide. In any event, such substitutions should employ amino acid residues or other molecular fragments chosen to avoid, for example, steric and charge interference which might disrupt binding.
• the substituting amino acids need not be limited to those naturally occurring in proteins, such as L- ⁇ -amino acids, or their D-isomers.
• the peptides may be substituted with a variety of moieties such as amino acid mimetics well known to those of skill in the art. (See, e.g., U.S. Pat. No. 6,030,619)
• a peptide bond mimetic of the invention includes peptide backbone modifications well known to those skilled in the art. Such modifications include modifications of the amide nitrogen, the ⁇ - carbon, amide carbonyl, complete replacement of the amide bond, extensions, deletions or backbone crosslinks. See, generally, Spatola, Chemistry and Biochemistry of Amino Acids, Peptides and Proteins, Vol. Nil (Weinstein ed., 1983). Several peptide backbone modifications are known.
• Amino acid mimetics may also be incorporated in the peptides.
• An "amino acid mimetic" as used here is a moiety other than a naturally occurring amino acid that conformationally and functionally serves as a substitute for an amino acid in a polypeptide of the present invention. Such a moiety serves as a substitute for an amino acid residue if it does not interfere with the ability of the peptide to illicit an immune response against the appropriate antigen.
• Amino acid mimetics may include non-protein amino acids, such as ⁇ y- ⁇ -amino acids, ⁇ - ⁇ - ⁇ -imino acids (such as piperidine-4-carboxylic acid), as well as many derivatives of L- ⁇ -amino acids.
• amino acid mimetics include cyclohexylalanine, 3-cyclohexylpropionic acid, L- adamantyl alanine, adamantylacetic acid and the like.
• Peptide mimetics suitable for peptides of the present invention are discussed by Morgan and Gainor, (1989) Ann. Repts. Med. Chem. 24: 243-2526.
• the peptides employed in the subject invention need not be identical, but may be substantially identical, to the corresponding sequence of the target antigen.
• the peptides may be subject to various changes, such as insertions, deletions, and substitutions, either conservative or non-conservative, where such changes might provide for certain advantages in their use.
• the polypeptides of the invention can be modified in a number of ways so long as they comprise a sequence substantially identical (as defined below) to a sequence in the target region of the antigen. Alignment and comparison of relatively short amino acid sequences (less than about
• Optimal alignment of sequences for aligning a comparison window may be conducted by the local homology algorithm of Smith and Waterman (1981) Adv. Appl. Math. 2:482, by the homology alignment algorithm of Needleman and Wunsch (1970) J. Mol Biol 48:443, by the search for similarity method of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. (USA) 85:2444, by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package Release 7.0, Genetics Computer Group, 575 Science Dr., Madison, WI), or by inspection, and the best alignment (i.e. resulting in the highest percentage of sequence similarity over the comparison window) generated by the various methods is selected.
• nucleic acids or polypeptide sequences refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or nucleotides that are the same, when compared and aligned for maximum correspondence, as measured using one of the following sequence comparison algorithms or by visual inspection.
• substantially identical in the context of two nucleic acids or polypeptides, refers to two or more sequences or subsequences that have at least 60%, preferably 80%, most preferably 90-95% nucleotide or amino acid residue identity, when compared and aligned for maximum correspondence, as measured using one of the following sequence comparison algorithms or by visual inspection.
• the substantial identity exists over a region of the sequences that is at least about 50 residues in length, more preferably over a region of at least about 100 residues, and most preferably the sequences are substantially identical over at least about 150 residues.
• the sequences are substantially identical over the entire length of the coding regions.
• sequence comparison typically one sequence acts as a reference sequence, to which test sequences are compared.
• test and reference sequences are input into a computer, subsequence coordinates are designated, if necessary, and sequence algorithm program parameters are designated.
• sequence comparison algorithm then calculates the percent sequence identity for the test sequence(s) relative to the reference sequence, based on the designated program parameters.
• Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Natl. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, WI), or by visual inspection (see generally, Current Protocols in Molecular Biology, F.M. Ausubel et al., eds., Current Protocols, a joint venture between Greene Publishing Associates, Inc. and John Wiley & Sons, Inc., (1995 Supplement) (Ausubel)).
• BLAST and BLAST 2.0 algorithms are described in Altschul et al. (1990) J. Mol. Biol. 215: 403-410 and Altschuel et al. (1977) Nucleic Acids Res. 25: 3389-3402, respectively.
• Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov/).
• This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et al, supra).
• initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them.
• the word hits are then extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always > 0) and N (penalty score for mismatching residues; always ⁇ 0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached.
• the BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment.
• the BLASTP program uses as defaults a wordlength (W) of 3, an expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff & Henikoff, Proc. Natl. Acad. Sci. USA 89:10915 (1989)).
• the BLAST algorithm In addition to calculating percent sequence identity, the BLAST algorithm also performs a statistical analysis of the similarity between two sequences (see, e.g., Karlin & Altschul, Proc. Natl. Acad. Sci. USA 90:5873-5787 (1993)).
• One measure of similarity provided by the BLAST algorithm is the smallest sum" probability (P(N)), which provides an indication of the probability by which a match between two nucleotide or amino acid sequences would occur by chance.
• P(N) the smallest sum probability
• a nucleic acid is considered similar to a reference sequence if the smallest sum probability in a comparison of the test nucleic acid to the reference nucleic acid is less than about 0.1, more preferably less than about 0.01, and most preferably less than about 0.001.
• a further indication that two nucleic acid sequences or polypeptides are substantially identical is that the polypeptide encoded by the first nucleic acid is immunologically cross reactive with the polypeptide encoded by the second nucleic acid, as described below.
• a polypeptide is typically substantially identical to a second polypeptide, for example, where the two peptides differ only by conservative substitutions.
• Another indication that two nucleic acid sequences are substantially identical is that the two molecules hybridize to each other under stringent conditions, as described below.
• residue positions which are not identical differ by conservative amino acid substitutions.
• Conservative amino acid substitutions refer to the interchangeability of residues having similar side chains.
• a group of amino acids having aliphatic side chains is glycine, alanine, valine, leucine, and isoleucine
• a group of amino acids having aliphatic-hydroxyl side chains is serine and threonine
• a group of amino acids having amide- containing side chains is asparagine and glutamine
• a group of amino acids having aromatic side chains is phenylalanine, tyrosine, and tryptophan
• a group of amino acids having basic side chains is lysine, arginine, and histidine
• a group of amino acids having sulfur- containing side chains is cysteine and methionine.
• Preferred conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine-valine, and asparagine-glutamine.
• Polypeptides encompassed by the invention typically comprise at least about 10 residues and more preferably at least about 15 residues, preferably from a domain of the antigen that is exposed to the immune system. In certain embodiments the peptides will not exceed about 50 residues and typically will not exceed about 30 residues.
• the immunogenic peptides are conformationally constrained.
• a preferred means for preparing conformationally constrained peptides is through cyclization. Any method commonly used to produce cyclized oligopeptides can be used to produce the peptides of the invention.
• the peptides will include cysteine residues at both termini, which allow the production of cyclic peptides through disulfide linkages.
• cyclic peptides Treatment of such a peptide with an oxidizing agent such as oxygen, iodine or similar agent will produce a cyclic peptide which may be further purified using chromatographic or other methods of chemical purification.
• Construction of cyclic peptides can also be accomplished through thioether linkages. For instance, N- bromoacetyl-derivatized peptides can be reacted with sulfhydryl-containing residues, such as cysteine. Cyclization occurs by reaction of the free sulfhydryl of cysteine in the peptide with the bromoacetyl group to form a thioether linkage (Robey et al., Anal. Biochem. Ill: 313-1 (1989) and U.S. Patent No. 5,066,716). Other methods of constructing cyclic peptides are known to those skilled in the art.
• linkers can be used to join the amino and carboxyl termini of a peptide.
• the linker is capable of forming covalent bonds to both the amino and carboxyl terminus.
• Suitable linkers are well known to those of skill in the art and include, but are not limited to, straight or branched-chain carbon linkers, heterocyclic carbon linkers, or peptide linkers.
• the linkers may be joined to the carboxyl and amino terminal amino acids through their side groups (e.g. through a disulfide linkage to cysteine) or through the alpha carbon amino and carboxyl groups of the terminal amino acids.
• cyclizations may include formation of carba analogs and thioethers (Lebl et al. in Peptides 1986 Proceedings of the 19th European Peptide Symposium pp. 341-344; Robey et al., Anal. Biochem. Ill: 373-7 (1989) and U.S. Patent No. 5,066,716), bis-thioethers (Mosberg et al.
• Bridging is a special type of cyclization in which distant sites in a peptide are brought together using separate bridging molecules or fragments.
• Bridging molecules may include, for example, succinic anhydride molecules (Charpentier, B., et al., supra), and carboxymethylene fragments (Thaisrivongs, S., et al., supra). Bridging by metals can also be used (Ozeki, E., et al., supra).
• the peptides include two or more cystine residues.
• the cystines can be substituted or added within the peptide or at either terminus.
• the position of the cystines is not critical so long as disulfide linkages can form between them which allow the production of cyclic peptides.
• treatment of such a peptide with an oxidizing agent such as oxygen, iodine or similar agent will produce a cyclic peptide which may be further purified using chromatographic or other methods of chemical purification.
• Additional embodiments include peptides containing antigenic sequences of protein sequences that have been incorporated into independently folding peptides (Regan & DeGrado, 1988, Science 241 :976; Mutter, 1988, TLBS 13 :260; Kamtekar et al., 1993, Science 262:1680; Sieber & Moe, 1996, Biochemistry 35:181; Butcher & Moe, 1996, Proc. Natl Acad. Sci. USA 93:1135; FitzGerald et al., 1998, Biochemistry 273:9951).
• the independently folding peptides may be naturally occurring or of de novo design.
• Peptides capable of eliciting protective immunity similar to that of the CHORI vaccine might also be obtained by using monoclonal antibodies produced by immunization with CHORI antigen or the like to select molecular mimetics from phage display peptide libraries or other combinatorial libraries such as small molecules or nucleic acids.
• antibodies raised against peptides of the invention can be used to inhibit inflammatory responses.
• Antibodies can be raised to the peptides of the present invention using techniques well known to those of skill in the art. Anti-idiotypic antibodies can also be generated. The following discussion is presented as a general overview of the techniques available; however, one of skill will recognize that many variations upon the following methods are known.
• the peptides and antibodies of the invention will be labeled by joining, either covalently or non-covalently, a substance which provides for a detectable signal. A wide variety of labels and conjugation techniques are known and are reported extensively in both the scientific and patent literature.
• Suitable labels include radionucleotides, enzymes, substrates, cofactors, inhibitors, fluorescent moieties, chemiluminescent moieties, magnetic particles, and the like. Patents teaching the use of such labels include U.S. Patents Nos. 3,817,837, 3,850,752, 3,939,350, 3,996,345, 4,277,437, 4,275,149 and 4,366,241. Also, recombinant immunoglobulins may be produced. See Cabilly, U.S. Patent No. 4,816,567; and Queen et al. (1989) Proc. Natl Acad. Sci. USA 86: 10029-10033. 6. Passive immunity
• Immunoprotective antibodies that recognize Neisserial epitopes can also be administered to an organism (e.g. a human patient) to induce passive immunity against a Neisserial disease, either to prevent infection or disease from occurring, or as a therapy to improve the clinical outcome in patients with established disease (e.g. decreased complication rate such as shock, decreased mortality rate, or decreased morbidity, such as deafness).
• an organism e.g. a human patient
• a therapy e.g. decreased complication rate such as shock, decreased mortality rate, or decreased morbidity, such as deafness.
• Antibodies administered to an organism other than the species in which they are raised are often immunogenic.
• murine or porcine antibodies administered to a human often induce an immunologic response against the antibody.
• the immunogenic properties of the antibody are reduced by altering portions, or all, of the antibody into characteristically human sequences thereby producing chimeric or human antibodies, respectively.
• Chimeric antibodies are immunoglobulin molecules comprising a human and non- human portion. More specifically, the antigen combining region (or variable region) of a humanized chimeric antibody is derived from a non-human source (e.g. murine), and the constant region of the chimeric antibody (which confers biological effector function to the immunoglobulin) is derived from a human source.
• the chimeric antibody should have the antigen binding specificity of the non-human antibody molecule and the effector function conferred by the human antibody molecule.
• a large number of methods of generating chimeric antibodies are well known to those of skill in the art (see, e.g., U.S. Patents Nos.
• recombinant DNA vector is used to transfect a cell line that produces an antibody against a peptide of the invention.
• the novel recombinant DNA vector contains a "replacement gene" to replace all or a portion of the gene encoding the immunoglobulin constant region in the cell line (e.g. a replacement gene may encode all or a portion of a constant region of a human immunoglobulin, or a specific immunoglobulin class), and a "target sequence” which allows for targeted homologous recombination with immunoglobulin sequences within the antibody producing cell.
• a recombinant DNA vector is used to transfect a cell line that produces an antibody having a desired effector function (e.g.
• the replacement gene contained in the recombinant vector may encode all or a portion of a region of an antibody and the target sequence contained in the recombinant vector allows for homologous recombination and targeted gene modification within the antibody producing cell.
• the resulting chimeric antibody may define the same antigen and/or have the same effector function yet be altered or improved so that the chimeric antibody may demonstrate a greater antigen specificity, greater affinity binding constant, increased effector function, or increased secretion and production by the transfected antibody producing cell line, etc.
• this invention provides for fully human antibodies.
• Human antibodies consist entirely of characteristically human polypeptide sequences.
• the human antibodies of this invention can be produced by a wide variety of methods (see, e.g., Larrick et al., U.S. Patent No. 5,001,065).
• the human antibodies of the present invention are produced initially in trioma cells (descended from three cells, two human and one mouse). Genes encoding the antibodies are then cloned and expressed in other cells, particularly non-human mammalian cells.
• trioma technology has been described by Ostberg et al. (1983), Hybridoma 2: 361-367, Ostberg, U.S. Patent No. 4,634,664, and Engelman et al., U.S. Patent No. 4,634,666.
• Triomas have been found to produce antibody more stably than ordinary hybridomas made from human cells.
• antibodies can be provided in a pharmaceutical composition comprising an effective amount of an antibody and a pharmaceutical excipients (e.g., saline).
• the pharmaceutical composition may optionally include other additives (e.g., buffers, stabilizers, preservatives, and the like).
• An effective amount of antibody is generally an amount effective to provide for protection against Neisserial disease or symptoms for a desired period, e.g., a period of at least about 2 days to 10 days or 1 month to 2 months).
• the antigens or antibodies of the invention can also be used for diagnostic purposes. For instance, peptides can be used to screen pre-immune and immune sera to ensure that the vaccination has been effective. Antibodies can also be used in immunoassays to detect the presence of particular antigen molecules associated with Neisserial disease.
• Strains for preparation of OMVS and MVs were selected on the basis of sergroup, serotype, and serosubtype. Strains to be used in the preparation of MVs were selected for relatively high levels of blebbing and expression of NspA (see Moe et al. (1999 Infect. Immun. 67: 5664). Exemplary strains used in preparation of OMVs and MVs have been deposited with the American Type Culture Collection (ATCC; see below). Strains that produce high levels of blebs, which strains are particularly useful in the MV production, can be selected or are known in the art (see, e.g., WO 01/34642).
• the meningococcal strain frozen at -80°C in aqueous -2% skim milk (w/v) was subcultured on a commercial chocolate agar plate (Remel, Laztakas, KS). After overnight growth at 37°C in 4% CO2, several colonies were selected to inoculate ⁇ 7 ml of sterile Mueller-Hinton broth to an OD 620nm of 0.1. The culture was incubated at 37°C, 4% CO2 with rocking until the OD620nm reaches 0.6-0.8 (two to three hours). Two to three 7 ml starter cultures were then used to inoculate 500 ml of Mueller-Hinton broth.
• the larger culture was grown to an OD 6 20nm of 0.9-1.0 at 37°C with vigorous shaking. Phenol is added to the culture to a final concentration of 0.5% (w/v) and the mixture is left at 4°C overnight to inactivate the bacteria. The cells were then pelleted by centrifugation (11,000 x g) for 30 min. at 4°C. The cell pellets were frozen at -20°C until used for preparation of outer membrane protein vesicles (OMV).
• OMV outer membrane protein vesicles
• Microvesicles were harvested from the phenol-treated cell culture supernatant by adding solid ammonium sulfate (390 g/1 final concentration) slowly with stirring. After the ammonium sulfate was added and completely dissolved, the mixture was left at 4°C overnight. The precipitated MNs were then collected by centrifugation at 11,000 x g for 30 min. The precipitated MN pellet was resuspended in 0.04 volume of PBS and centrifuged again at 16,000 x g for 15 min. at 4°C. The pellet was discarded and the MNs, which remain in the supernatant, were collected by centrifugation at 100,000 x g for 2 hrs. at 4°C.
• the final pellet was resuspended in 0.01 volume (i.e. 5 ml per 500 ml of culture) of water ("MV" vaccine preparation).
• the pellet was resuspended in 0.1M TrisrHCl, pH 8.6, containing 10 mM EDTA and 0.5% (w/v) sodium deoxycholate ( ⁇ 3 ml/500 ml cell culture). After stirring (30 min), the mixture was centrifuged (125,000 x g, 2 hrs, 4°C). The supernatant was discarded and the pellet resuspended.in 1 ml of 3% sucrose ("DOC MV" vaccine preparation).
• the protein concentration of the MN and DOC MN preparations was determined by BCA assay (Pierce Chemical Co., Rockford, JL). The MN and DOC MN suspensions were then frozen on dry ice and stored at -20°C until used for immunization. Outer membrane vesicles (OMN) were prepared by the method of Zollinger et al. (1979 J. Clin. Invest. 63: 836-848). The frozen cell pellet was resuspended in 10 ml of 0.05 M Tris ⁇ Cl buffer, pH 7.4 containing 0.15 M ⁇ aCl and 0.01 M EDTA then heated to 56°C for 30 min. followed by cooling on ice.
• the cell suspension was then sonicated on ice with several 15-second bursts using a microprobe sonifier (Branson, Danbury, CT). Cell debris was removed by centrifugation at 16,000 x g for 15 min., and the outer membrane vesicles (OMNs) in the supernatant were obtained by ultracentrifugation at 100,000 x g for 2 hrs. at 4°C.
• the OMN pellet was resuspended in 2 ml of water ("OMV" vaccine preparation).
• the frozen cell pellet was resuspended in 0.1M Tris»HCl, pH 8.6, containing 10 mM EDTA and 0.5% (w/v) sodium deoxycholate.. After stirring for 30 min.
• the mixture was centrifuged (20,000 x g, 30 min., 4°C). The supernatant was retained and the pellet was reextracted and centrifuged again with one third volume of the same buffer. The supernatants from both extractions were combined and centrifuged (125,000 x g, 2 hrs, 4°C). The supernatant was discarded and the pellet was resuspended in 5 ml of 3% sucrose ("DOC OMN" vaccine preparation). The OMV and DOC OMV vaccine preparations were frozen on dry ice, and stored at -20°C until used for immunization. The protein concentration of the OMV and DOC OMV preparations was determined by BCA (Pierce Chemical Co., Rockford, EL).
• MV or OMN preparations were diluted in PBS and either mixed with an equal volume of complete Freund's adjuvant (CFA; Sigma Chemical Company, St. Louis, MO) or aluminum hydroxide (Alhydrogel 1.3% from Superfos Biosector, Frederikssund, Denmark), or aluminum phosphate (Alhydrogel that had been incubated with PBS buffer for at least 3 hrs).
• CFA complete Freund's adjuvant
• Alhydrogel 1.3% from Superfos Biosector, Frederikssund, Denmark
• aluminum phosphate Alhydrogel that had been incubated with PBS buffer for at least 3 hrs.
• CpG nucleotides 5'-TCCATGACGTTCCTGACGTT- 3' (SEQ ID ⁇ O.l) Chiron Corp., Emeryville, CA) were added to the aluminum phosphate/antigen mixture to a final concentration of 100 ⁇ g/ml as a second adjuvant.
• mice were immunized by the IP (CFA) or SC (aluminum phosphate, aluminum hydroxide) routes with 100 ⁇ l containing between 5 to 25 micrograms of total protein of the MN prepared from the meningococcal strain RMI 090.
• CFA IP
• SC aluminum phosphate, aluminum hydroxide
• CHORI vaccine The sequential immunization with three different meningococcal strains, which were genetically different with respect to their serogroup, serotype, and serosubtype and other antigens constitutes what is hereafter designated "CHORI vaccine".
• CHORI vaccine Another group of mice were immunized with CHORI vaccine as described above except that CpG oligonucleotides were not used as a second adjuvant and the experiment included mice that were given the CHORI vaccine combined with aluminum hydroxide adjuvant and mice that were given three injections of a mixture of the MV/OMV described above together with aluminum phosphate.
• groups of guinea pigs were given either sequential immunizations with CHORI vaccine antigens or three injections of a mixture of CHORI vaccine antigens combined with aluminum phosphate.
• Protein preparations were analyzed using 15% SDS-PAGE as described by Laemmli (1970 Nature 227: 680-685) employing a Mini-Protean II electrophoresis apparatus (Bio- Rad, Richmond, CA). Samples were suspended in SDS sample buffer (0.06 M Tris»HCl, pH 6.8, 10% (v/v) glycerol, 2% (w/v) SDS, 5% (v/v) 2-mercaptoethanol, 10 micrograms /ml bromophenol blue) and optionally heated to 100°C for 1 min. before loading directly onto the gel.
• SDS sample buffer (0.06 M Tris»HCl, pH 6.8, 10% (v/v) glycerol, 2% (w/v) SDS, 5% (v/v) 2-mercaptoethanol, 10 micrograms /ml bromophenol blue
• Figure 2 shows a Coomassie-stained 15% SDS-PAGE gel of the proteins present in the MN of strain Z1092 (lane 2) or OMN preparations from strain Z1092 (lane 4), or the respective preparations after having been extracted with 0.5% (w/v) sodium deoxycholate (i.e. DOC MN [lane 3] and DOC OMN [lane 5]) as described by Fredricksen et al. (1991, NIPHAnn. 14: 67-79).
• the four corresponding preparations made from meningococcal strains BZ198 and RM1090 are shown in lanes 6 to 13, respectively).
• PorA, PorB, Rmp, Opa, and Ope Five proteins, PorA, PorB, Rmp, Opa, and Ope, are known to constitute the major outer membrane proteins of Neisseria meningitidis. All of the preparations appear to contain the major outer membrane proteins PorA and PorB (-39-42 kDa) and the opacity proteins, Opa and Ope (-28-31 kDa), although the apparent mass of the particular proteins and relative amounts were different in each preparation. The less distinct protein having an apparent mass of -31-34 kDa in the DOC OMN preparations may be reduction modifiable protein (Rmp). In addition to these major outer membrane proteins, each MN and OMN preparation contains various other proteins in lesser amounts. In general, the minor proteins are more variable between strains and between MN compared to OMV preparations. D. Antibody binding to the cell surface
• Binding of antibodies to the surface of live bacteria was determined by indirect fluorescence flow cytometry (Granoff et al., 1998, J. Immunol. 160: 5028-5036).
• Bacterial cells were grown to mid-log phase in Mueller-Hinton broth, harvested by centrifugation, and resuspended in blocking buffer (PBS containing 1% (w/v) bovine serum albumin (BSA) and 0.4% (w/v) sodium azide) at a density of -10 8 cells per ml.
• Dilutions of test or control antiserum typically 1 :20, 1 :200, 1 :2000
• test or control antiserum typically 1 :20, 1 :200, 1 :2000
• Positive control antibodies included meningococcal-specific serotyping or serosubtyping monoclonal antibodies (M ⁇ 2C3B, MN16C13F4, Rijksinstituut Voor Herbstgezondheid en Mileu, Bilthoven, The Netherlands) and SEAM 12, an anti- polysaccharide monoclonal antibody that is specific for encapsulated serogroup B strains (Granoff et al., 1998, J. Immunol. 160:5028).
• the negative control consisted of a mouse IgG monoclonal antibody (VIGIO) of irrelevant specificity and polyclonal sera from mice immunized with membrane proteins from E. coli.
• Antibodies used to define serogroup, serotype, and serosubtype are provided in Figures 20 and 21.
• Figure 3 shows the results of a typical experiment examining antibody binding to two test strains: MC58 and S3446. Both strains express PorA and PorB proteins that are heterologous with the respective porin protein s from the three strains used to prepare the CHORI vaccine.
• the antisera from mice immunized with CHORI antigen show an increase in fluorescence intensity with both strains when the antisera were tested at dilutions of 1 :20 to 1:200.
• polyclonal antisera prepared to proteins precipitated from culture supernatant of the ?. coli show only low intensity background fluorescence (1:20 dilution), and were considered negative.
• bactericidal assay was adapted from the method previously described by Mandrell et al. (1995 J. Infect. Dis. 172: 1279-1289). Finding that a vaccine produces bactericidal antibodies against Neisseria meningitidis is accepted in the field as predictive of the vaccine's protective effect in humans (Goldschneider et al., 1969, J. Exp. Med. 129: 1307; Borrow et al. 2001 Infect Immun. 69:1568). After overnight growth on chocolate agar, several colonies were inoculated into Mueller-Hinton broth (starting A62Qnm of -0.1) and the test organism was grown for approximately 2 hrs.
• CFUs colony forming units
• the final reaction mixture of 60 microliters contained 20% (v/v) complement, and serial 2-fold dilutions of test sera or control monoclonal antibodies in Gey's buffer.
• the complement source was human serum from a healthy adult with no detectable anticapsular antibody to serogroup B polysaccharide when tested by ELISA (Granoff et al., 1998, J. Immunol. 160: 5028-5036), and no detectable intrinsic bactericidal activity against the test strain at a final concentration of 20 or 40%.
• this complement source gave comparable bactericidal titers as those obtained with agammaglobulinemic serum as the complement source.
• Serum bactericidal titers were defined as the serum dilution (or antibody concentration) resulting in a 50% decrease in CFUs per ml after 60 min. incubation of bacteria in the reaction mixture, compared to the control CFU per ml at time 0.
• bacteria incubated with the negative control antibody end complement showed a 150 to 200% increase in CFU/mL during the 60 min. of incubation.
• Figure 6 shows data from a typical experiment with meningococcal B strain 2996 tested with an anti-meningococcal B capsular mAb (SEAM 12, Granoff et al., 1998, J. Immunol. 160: 5028-5036), mouse and guinea pig control antisera, mouse anti-recombinant NspA and anti-CHORI antigen antisera, and guinea pig anti-Norwegian vaccine antisera.
• Figure 7 summarizes the results of measurement of complement-mediated bactericidal activity of the anti-CHORI antigen antisera to each of the menigococcal B strains tested.
• Figure 8 summarizes the results of testing complement-mediated bactericidal activity of anti-CHORI antisera prepared in a second experiment in mice. Data are shown for antisera prepared with CHORI vaccine given with CFA or aluminum phosphate (without CpG). The results are shown for the 14 meningococcal B strains tested in this experiment (8 with serosubtypes heterologous to those of the vaccine strains). Results also are shown for one additional MenB strain in which the gene encoding NspA has been inactivated (BZ198 ⁇ Ns ⁇ A). All 15 strains were killed by anti-CHORI antisera (14/15 with CHORI vaccine given with CFA; and 13/15 with CHORI vaccine given with aluminum phosphate; for the heterologous strains, 6/7 and5/7, respectively).
• mice in the second experiment received three injections, each consisting of a mixture of the same MV, MV and OMV used in the sequential immunization.
• the resulting antisera were bactericidal against 12 of the 15 strains (4 of 7 of the heterologous strains). Immunization with the mixture of antigens elicited broader bactericidal activity than expected but the titers measured against the some strains tended to be much lower than those obtained in animals given the sequential CHORI vaccine immunization (e.g. strains CU385 and 1000, titers of 1:128 and 1:128 after CHORI vaccine/alumunium phosphate vs. titers of ⁇ 1:4 and 1:6 in antisera prepared against three injections of the mixed CHORI vaccine immunization (e.g. strains CU385 and 1000, titers of 1:128 and 1:128 after CHORI vaccine/alumunium phosphate vs. titers of ⁇ 1:4 and 1:6 in
• the meningococcal B strain 8047 which was positive by the flow cytometric assay for CHORI antigen-surface accessible epitopes and susceptible to anti-CHORI antigen bactericidal activity, was selected for this study.
• Infant pups (6- to 7-day old) from six litters of outbred Wistar rats (Charles River, Hollister, CA) were randomly redistributed to the nursing mothers. Groups of five to six animals were challenged D? with 100 ⁇ l of approximately 5 x 10 3 CFU of the group B strain 8047.
• the strain used ' had been passaged three times in infant rats.
• the bacteria isolated from blood cultures after the third pass was grown on chocolate agar overnight and stored frozen at -70°C in vials containing sterile skim milk. On the day of the experiment, the bacteria were grown, washed and resuspended in PBS buffer containing 1% BSA, as described above for the bactericidal assay.
• the animals were given antisera or antibodies diluted in PBS containing 1% BSA by IP injection 2 hrs. prior to bacterial challenge.
• blood specimens were obtained by puncturing the heart with a syringe and needle containing one to two drops of 25 Units/ml of heparin without preservative (Fujisawa USA, Deerfield, IL).
• Aliquots of 1, 10 and 100 microliters of blood were plated onto chocolate agar.
• the CFU per ml of blood was determined after overnight incubation of the plates at 37°C in 5% CO 2 .
• Figure 10 summarizes the results of quantitative bacterial cultures performed on blood specimens obtained 18 hrs. after challenge.
• the guinea pig anti- Norwegian vaccine antisera (1 :20) and the two control sera were not able to protect against bacteremia caused by strain 8047.
• anti- CHORI vaccine antisera prepared in guinea pigs were also shown to protect infant rats from meningococcal B bacteremia after D? challenge (Figure 11). Protection was observed in animals treated with antisera prepared to vaccine administered with aluminum phosphate or aluminum hydroxide, and was superior to the protection observed in control animals treated with 20 ⁇ g of a murine anticapsular monoclonal antibody (SEAM 3).
• the method used for immunoprecipitation of surface-accessible antigens was based on those described by Hansen et al. (1981 Infect. Immun. 33: 950-953) and Gulig et al. (1982 Infect. Immun. 37: 82-88). In our studies, the method was used with either unlabeled cells, or with cells in which the surface proteins had had been radioiodinated. Cells were grown in Mueller-Hinton broth (-7 ml) to an OD of 0.6 and harvested by centrifugation at 5000 x g at 4°C. The cell pellet was washed two times in cold PBS containing 1% BSA or, for the radioimmunoprecipitation assay, PBS alone.
• the cells were resuspended in PBS (2 ml) containing 1% BSA.
• the antisera were added to 0.5 ml aliquots of cell suspension.
• the mixture was incubated with rocking for 90 min. at 4°C.
• the cells were then collected by centrifugation (1 min. spin in microfuge), washed two times with PBS/1% BSA, and resuspended in 1 ml of solubilization buffer (50 mM Tris buffer, pH 7.8, containing 150 mMNaCl, 1 mMEDTA, 1% Triton X-100, 0.2 % sodium deoxycholate, and 0.1 % sodium dodecyl sulfate. After incubation for 60 min.
• solubilization buffer 50 mM Tris buffer, pH 7.8, containing 150 mMNaCl, 1 mMEDTA, 1% Triton X-100, 0.2 % sodium deoxycholate, and 0.1 % sodium do
• the insoluble material was removed by centrifugation (45,000 x g for 60 min. at 20°C).
• the superaatants were then transferred to tubes containing 3-4 milligrams of protein A Sepharose beads (Sigma) pre-equilibrated with 50 ⁇ l of PBS.
• the samples were incubated overnight at 4°C with rocking.
• the beads were washed five times with solubilization buffer. Bound proteins were released from the beads by adding 75 ⁇ l of SDS sample buffer and heated to 100°C for 1 min. After removing the supernatant, 1 ⁇ l of 2-mercapto ethanol was added to each sample and then heated again to 100°C for 1 min.
• the samples were then run on a 15%» SDS-PAGE gel and stained using silver stain (Pierce Chemical Co., Rockford, IL).
• the gel was equilibrated with buffer (48 mM TrisrHCl, 39 mM glycine, pH 9.0, 20% (v/v) methanol) and the proteins were transferred to a nitrocellulose membrane (Bio-Rad) using a Trans-Blot ⁇ M (Bio-Rad) semi-dry electrophoretic transfer cell.
• the nitrocellulose membranes were blocked with 2% (w/v) skim milk in PBS containing 0.2% (w/v) sodium azide. Antisera were diluted in the same blocking buffer containing 0.1% Tween-20.
• Bound antibody was detected using rabbit anti-mouse IgG,A,M-alkaline phosphatase conjugate polyclonal antibody (Zymed, South San Francisco, CA) diluted in PBS containing 1% (w/v) BSA, 1% (w/v) Tween-20, and 0.2% (w/v) sodium azide and Sigma FastTM BCIP/NBT substrate (Sigma).
• Figure 12 is a silver-stained SDS gel demonstrating cell surface proteins precipitated with the anti-CHORI antisera (Lane 2) from M7, a non-encapsulated mutant of serogroup B strain, NMB (Stephens et al. 1991, Infect. Immun. 59- 4097-4107).
• six proteins having apparent masses of 59.5, 40.7. 39.6, 33, 27.9, and 14.5 kDa were precipitated by the antisera prepared to the CHORI antigen (Lane 2) but not by control anti-£. coli protein antisera (Lane 3).
• the same results were obtained when the anti-CHORI antigen antisera were used to precipitate surface proteins from the encapsulated parent strain, NMB (data not shown). Except for the 59.5 and 27.9 kDa heavy and light chain Ig proteins (see below), the same surface proteins detected by silver staining were observed also in ⁇ I-labeled cells (data not shown).
• FIG. 13 shows a Western blot of the same samples as resolved on the SDS gel in Figure 12. Samples in lanes 1 to 3 were detected by anti-CHORI vaccine antisera. Samples in Lanes 4 to 6 were detected by an anti-PorA PI .2-specific mAb.
• the proteins having apparent masses of 59.5 and 27.9 kDa in Figure 13, correspond to antibody heavy and light chains, respectively, as they were detected with the rabbit anti- mouse Ig alkaline phosphatase conjugate secondary antibody.
• the 40.7 kDa protein precipitated by the anti-CHORI antigen antisera (Figure 12, Lane 2) was reactive with the anti-PorA PI.2-specific antibody in the Western ( Figure 13, Lane 5) and is, therefore, PorA PI .2.
• PorA PI .2 also was detected in the total protein from M7 ( Figure 13, Lane 4).
• the anti-CHORI vaccine antisera detected only the 33 kDa protein (Lane 2) and not PorA.
• the antisera prepared to the CHORI antigen reacts with both native and denatured 33 kDa protein but only native forms of the 40.7. 39.6, and 14.5 kDa proteins present on the cell surface of strain M7 ( Figure 12, lane 2).
• proteins having an apparent mass of 25.7 kDa were precipitated from strains NG3/88 and S3446 but not from any other strains.
• the 32 to 33 kDa protein may be a conserved antigen.
• Figure 15 shows a Western blot of MVs from strains RM1090 (C:2a:P1.5,2:L3,7), and BZ198 (B.NT.P1.4) and OMV from strain Z 1092 (A:4:P1.10).
• the blot shows that the CHORI vaccine elicits antibodies that are reactive with several proteins having similar apparent molecular mass in each of the MV or OMV preparations independent of the animal species or adjuvant used in the vaccine.
• the apparent molecular masses of all proteins in the MV or OMV preparations that are reactive with antibodies produced by immunization with CHORI vaccine are summarized in Figure 16.
• LOS lipooligosaccharide
• LOS (1 mg) was combined with BSA (2 mg) in 100 mM MES buffer, pH 5.0: EDC (l-ethyl-3- (3- dimehtylaminopropyl) carbodiimide HCl; 100 ⁇ l of a 10 mg/ml solution in water) was added with stirring followed by incubation at ambient temperature for 2 hrs.
• An equal mixture of the three LOS-BSA conjugates (1 mg LOS-BSA conjugate per ml of hydrated gel) was coupled to CNBr-activated agarose beads (Sigma Chemical Co., St. Louis, MO) in sodium carbonate buffer (0.1 M, pH 8.0) overnight at ambient temperature.
• the antisera After removal of anti-LOS antibodies by passing the anti-CHORI vaccine and anti- CHORI mixed antigen antisera through the LOS affinity column, the antisera were concentrated to their original volume by ultrafiltration and tested for the presence of anti- LOS antibody by ELISA and complement-mediated bactericidal activity against two MenB strains (BZ198 and S3032). As summarized in Figure 17, the presence of anti-LOS antibody was greatly reduced or eliminated by absorption with the LOS-BSA conjugate affinity column.
• mice prepared from meningococcal strain RM1090 (C:2a:P1.5,2), BZ198 (B:NT:7,4), and OMV from strain Z1092 (A:4,21:P1.10).
• the mice were given three 100 microliters injections, each separated by three weeks, containing 5 micrograms of protein.
• the first two doses were given subcutaneously together with aluminum phosphate (0.5% wt/vol) and the final dose was given without adjuvant and administered intraperitoneally (i.p.).
• the animals were sacrificed and their spleen cells were fused with myeloma cells (P3X63-AG8.653) at a ratio of 1 spleen cell to 1.7 myeloma cell.
• hybridoma superaatants were screened for antibody binding activity by whole cell ELISA using encapsulated MenB strains 1000 and CU385 as the target antigen.
• Hybridomas secreting antibody that was reactive with both 1000 and CU385 strains in a whole cell ELISA and were positive for binding by flow cytometry were cloned by limiting dilution and then expanded and frozen for subsequent use in tissue culture.
• Antibodies from eight cell lines were characterized in detail.
• the subclasses of the monoclonal antibodies were determined using an antibody capture ELISA and alkaline phosphatase-conjugated polyclonal antibody specific for each of the mouse IgG subclasses, IgM, IgA, and K and ⁇ light chains (Southern Biotechnology Associates, Inc. Birmingham, Ala.).
• the monoclonal antibodies produced by the hybridoma clones were harvested from tissue culture media by ammonium sulfate precipitation (55% wt/vol). The concentration of the purified mAb was determined by capture ELISA using Ig standards as recommended by the manufacturer (Southern Biotechnology Associates, Inc. Birmingham, Ala.).
• This mAb also is reactive with strains 8047 and BZ198 but is not reactive with the corresponding strains in which the NspA gene has been inactivated.
• antigens recognized by the mAbs 4B11 and 9B6 are limited to certain strains.
• MAb 4B11 is reactive with strain 8047 but not with the corresponding 8047 mutant in which the NspA gene has been inactivated.
• mAb 4B11 does not bind to rNspA expressed in E. coli vesicles, and also does not bind to strain BZ198, which is known to naturally overexpress (see Moe et al. (1999 Infect. Immun. 67: 5664; Moe et al.
• mAb 4B11 may recognize a NspA epitope that is specific to strain 8047, or an epitope on another membrane protein that is not present in strain BZ198 but is present and associated with NspA expression in strain 8047.
• the results with the different mAbs show that the anti-CHORI antigen vaccine elicits antibodies against both highly conserved and non-conserved proteins.
• the complement-mediated bactericidal activity of mAbs prepared from mice immunized with anti-CHORI antigen and tested against several MenB strains is summarized in Figure 20.
• the monoclonal antibody 1D9 which reacts by ELISA with all N. meningitides strains tested, was not bactericidal.
• the monoclonal antibody 14C7 which appears to recognize ⁇ spA, was bactericidal or bacteriostatic against all strains tested except BZ198 ⁇ spA (a knockout of NspA).
• the activity of the 14C7 monoclonal antibody was superior to that of the control monoclonal antibody AL12 (produced in mice immunized with recombinant NspA (see Moe et al. Infect Immun.
• the monoclonal antibody 4B11 (an IgM antibody) was bactericidal against strains 1000 and CU385. Note that the 4B11 monoclonal antibody did not react with these same strains by whole-cell ELISA at the highest concentration tested (see Figure 19).
• the bactericidal assays measures functional antibody activity using live bacteria whereas the bacterial cell ELISA measures antibody binding to heat-killed bacteria, which in these strains may have denatured the antigenic target of mAb 4B11.
• the designated deposits will be maintained for a period of thirty (30) years from the date of deposit, or for five (5) years after the last request for the deposit; or for the enforceable life of the U.S. patent, whichever is longer. Should a culture become nonviable or be inadvertently destroyed, or, in the case of plasmid-containing strains, lose its plasmid, it will be replaced with a viable culture(s) of the same taxonomic description.

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