US20030180316A1 - Multivalent vaccine composition - Google Patents

Multivalent vaccine composition Download PDF

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Publication number
US20030180316A1
US20030180316A1 US10/312,090 US31209003A US2003180316A1 US 20030180316 A1 US20030180316 A1 US 20030180316A1 US 31209003 A US31209003 A US 31209003A US 2003180316 A1 US2003180316 A1 US 2003180316A1
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capsular polysaccharide
immunogenic composition
pneumoniae serotype
group
meningitidis
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Dominique Boutriau
Carine Capiau
Pierre Desmons
Dominique Lemoine
Jan Poolman
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GlaxoSmithKline Biologicals SA
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GlaxoSmithKline Biologicals SA
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Priority claimed from GBGB0015999.6A external-priority patent/GB0015999D0/en
Priority claimed from GBGB0108364.1A external-priority patent/GB0108364D0/en
Priority claimed from GB0108363A external-priority patent/GB0108363D0/en
Application filed by GlaxoSmithKline Biologicals SA filed Critical GlaxoSmithKline Biologicals SA
Assigned to GLAXOSMITHKLINE BIOLOGICALS S.A. (FORMERLY SMITHKLINE BEECHAM BIOLOGICALS S.A.) reassignment GLAXOSMITHKLINE BIOLOGICALS S.A. (FORMERLY SMITHKLINE BEECHAM BIOLOGICALS S.A.) ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DESMONS, PIERRE MICHEL, POOLMAN, JAN, BOUTRIAU, DOMINIQUE, LEMOINE, DOMINIQUE, CAPIAU, CARINE
Publication of US20030180316A1 publication Critical patent/US20030180316A1/en
Priority to US13/439,829 priority Critical patent/US9233151B2/en
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    • A61K39/0016—Combination vaccines based on diphtheria-tetanus-pertussis
    • A61K39/0018—Combination vaccines based on acellular diphtheria-tetanus-pertussis
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    • A61K2039/60—Medicinal preparations containing antigens or antibodies characteristics by the carrier linked to the antigen
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    • A61K2039/70—Multivalent vaccine
    • C—CHEMISTRY; METALLURGY
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    • C12N2730/00—Reverse transcribing DNA viruses
    • C12N2730/00011—Details
    • C12N2730/10011—Hepadnaviridae
    • C12N2730/10111—Orthohepadnavirus, e.g. hepatitis B virus
    • C12N2730/10134—Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention relates to new combination vaccine formulations.
  • Combination vaccines which provide protection against multiple pathogens
  • the well-documented phenomenon of antigenic competition (or interference) complicates the development of multi-component vaccines.
  • Antigenic interference refers to the observation that administering multiple antigens often results in a diminished response to certain antigens relative to the immune response observed when such antigens are administered individually.
  • Combination vaccines are known which can prevent Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae , and optionally Hepatitis B virus and/or Haemophilus influenzae type b (see, for instance, WO 93/24148 and WO 97/00697).
  • the present invention concerns the manufacture of the most ambitious multi-valent vaccines to date, the administration of which can prevent or treat infection by Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae , Hepatitis B virus, Haemophilus influenzae and N. meningitidis , and preferably also Hepatitis A virus and/or Polio virus, wherein the components of the vaccine do not significantly interfere with the immunological performance of any one component of the vaccine.
  • the present invention provides a multi-valent immunogenic composition for conferring protection in a host against disease caused by Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae , Hepatitis B virus, Haemophilus influenzae and N. meningitidis comprising:
  • Hepatitis B surface antigen HepB
  • a carrier protein selected from the group N. meningitidis type A (MenA) and N. meningitidis type C (MenC).
  • TT tetanus toxoid
  • TT is preferably produced by purification of the toxin from a culture of Clostridium tetani followed by chemical detoxification, but is alternatively made by purification of a recombinant, or genetically detoxified analogue of the toxin (for example, as described in EP 209281).
  • Tetanus toxoid also encompasses immunogenic fragments of the fill-length protein (for instance Fragment C—see EP 478602).
  • DT diphtheria toxoid
  • DT is preferably produced by purification of the toxin from a culture of Corynebacterium diphtheriae followed by chemical detoxification, but is alternatively made by purification of a recombinant, or genetically detoxified analogue of the toxin (for example, CRM197, or other mutants as described in U.S. Pat. Nos. 4,709,017, 5,843,711, 5,601,827, and 5,917,017).
  • Acellular pertussis components are well known in the art. Examples include pertussis toxoid (PT), filamentous haemagluttinin (FHA), pertactin (PRN) and agglutinogens 2 and 3. These antigens are partially or highly purified. Preferably 2 or more acellular pertussis components are used in the vaccine. More preferably 2, 3, 4 or all 5 of the above example acellular pertussis components are incorporated in the vaccine. Most preferably PT, FHA and PRN are included. PT may be produced by a variety of manners, for instance by purification of the toxin from a culture of B. pertussis followed by chemical detoxification, or alternatively by purification of a genetically detoxified analogue of PT (for example, as described in U.S. Pat. No. 5,085,862).
  • the bacterial capsular polysaccharide conjugates may comprise any carrier peptide, polypeptide or protein comprising at least one T-helper epitope.
  • the carrier protein(s) used is selected from the group comprising: tetanus toxoid, diphtheria toxoid, CRM197, recombinant diphtheria toxin (as described in any of U.S. Pat. No. 4,709,017, WO 93/25210, WO 95/33481, or WO 00/48638), pneumolysin (preferably chemically detoxified, or a detoxified mutant) from S. pneumoniae , OMPC from N. meningitidis , and protein D (PD) from H.
  • the polysaccharide antigens contained therein are conjugated to more than one carrier.
  • (n ⁇ 1) of the polysaccharides could be carried (separately) on one type of carrier, and 1 on a different carrier, or (n ⁇ 2) on one, and 2 on two different carriers, etc.
  • 1, 2 or all four could be conjugated to different carriers).
  • Protein D is advantageously used as a carrier in the compositions of the invention as it may be used for various (2, 3, 4 or more) polysaccharides in a composition without a marked carrier suppression effect. Most preferably Hib is present as a TT conjugate, and MenA, MenC, MenY and MenW are either TT or PD conjugates. Protein D is also a useful carrier as it provides a further antigen which can provide protection against H influenzae.
  • the polysaccharide may be linked to the carrier protein by any known method (for example, by Likhite, U.S. Pat. No. 4,372,945 and by Armor et al., U.S. Pat. No. 4,474,757).
  • CDAP conjugation is carried out (WO 95/08348).
  • the cyanylating reagent 1-cyano-dimethylaminopyridinium tetrafluoroborate (CDAP) is preferably used for the synthesis of polysaccharide-protein conjugates.
  • the cyanilation reaction can be performed under relatively mild conditions, which avoids hydrolysis of the alkaline sensitive polysaceharides. This synthesis allows direct coupling to a carrier protein.
  • the above immunogenic composition may further comprise one, two, three, four, five, six or seven components selected from the following list: N. meningitidis type Y polysaccharide [MenY] (preferably conjugated), N. meningitidis type W polysaccharide [MenW] (preferably conjugated), the Vi polysaccharide of Salmonella typhi, N. meningitidis (preferably serotype B) outer membrane vesicles, one or more N.
  • N. meningitidis type Y polysaccharide [MenY] preferably conjugated
  • N. meningitidis type W polysaccharide [MenW] preferably conjugated
  • the Vi polysaccharide of Salmonella typhi preferably serotype B
  • N. meningitidis preferably serotype B
  • meningitidis preferably serotype B
  • outer membrane surface-exposed proteins
  • killed attenuated Hepatitis A virus (HepA—preferably the product known as ‘HavrixTM’ [SmithKline Beecham Biologicals]
  • IPV inactivated polio virus
  • types 1, 2 and 3 as is standard in the vaccine art, most preferably the Salk polio vaccine
  • the immunogenic compositions of the invention are preferably formulated as a vaccine for in vivo administration to the host in such a way that the individual components of the composition are formulated such that the immunogenicity of individual components is not substantially impaired by other individual components of the composition.
  • substantially impaired it is meant that upon immunisation, an antibody titre against each component is obtained which is more than 60%, preferably more than 70%, more preferably more than 80%, still more preferably more than 90%, and most preferably more than 95-100% of the titre obtained when the antigen is administered in isolation.
  • the immunogenic compositions of the invention are preferably formulated as a vaccine for in vivo administration to the host, such that they confer an antibody titre superior to the criterion for seroprotection for each antigenic component for an acceptable percentage of human subjects. This is an important test in the assessment of a vaccine's efficacy throughout the population. Antigens with an associated antibody titre above which a host is considered to be seroconverted against the antigen are well known, and such titres are published by organisations such as WHO. Preferably more than 80% of a statistically significant sample of subjects is seroconverted, more preferably more than 90%, still more preferably more than 93% and most preferably 96-100%.
  • the immunogenic composition of the invention are preferably adjuvanted.
  • Suitable adjuvants include an aluminium salt such as aluminium hydroxide gel (alum) or aluminium phosphate, but may also be a salt of calcium, iron or zinc, or may be an insoluble suspension of acylated tyrosine, or acylated sugars, cationically or anionically derivatised polysaccharides, or polyphosphazenes.
  • the adjuvant may also be selected to be a preferential inducer of a TH1 type of response to aid the cell mediated branch of the immune response.
  • Th1-type cytokines tend to favour the induction of cell mediated immune responses to a given antigen, whilst high levels of Th2-type cytokines tend to favour the induction of humoral immune responses to the antigen.
  • Suitable adjuvant systems which promote a predominantly Th1 response include, Monophosphoryl lipid A or a derivative thereof, particularly 3-de-O-acylated monophosphoryl lipid A, and a combination of monophosphoryl lipid A, preferably 3-de-O-acylated monophosphoryl lipid A (3D-MPL) together with an aluminium salt.
  • An enhanced system involves the combination of a monophosphoryl lipid A and a saponin derivative, particularly the combination of QS21 and 3D-MPL as disclosed in WO 94/00153, or a less reactogenic composition where the QS21 is quenched with cholesterol as disclosed in WO 96/33739.
  • a particularly potent adjuvant formulation involving QS21, 3D-MPL and tocopherol in an oil in water emulsion is described in WO 95/17210.
  • the vaccine may additionally comprise a saponin, more preferably QS21.
  • the formulation may also comprises an oil in water emulsion and tocopherol (WO 95/17210).
  • Unmethylated CpG containing oligonucleotides (WO 96/02555) are also preferential inducers of a TH1 response and are suitable for use in the present invention.
  • Aluminium salts are preferred adjuvants in the above immunogenic compositions.
  • HepB should preferably be adsorbed onto aluminium phosphate before admixing with the other components.
  • the polysaccharide conjugates may be unadjuvanted.
  • the present invention also provides a method for producing a vaccine formulation comprising the step of mixing the components of the vaccine together with a pharmaceutically acceptable excipient.
  • a particularly preferred DTPw composition of the invention comprises: TT, DT, Pw, HepB (preferably adsorbed onto aluminium phosphate), Hib (preferably conjugated onto TT and/or unadsorbed), MenA (preferably conjugated onto protein D), and MenC (preferably conjugated onto protein D).
  • the vaccine may be supplied in 2 containers, the first containing DTPw-HepB in a liquid form, and a second containing Hib-MenA-MenC in a lyophilised form. The contents of the containers may be mixed extemporaneously before administering to a host in a single injection.
  • an immunogenic composition or vaccine as herein described for use in a medicament.
  • a method of immunising a human host against disease caused by Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae , Hepatitis B virus, Haemophilus influenzae and N. meningitidis which method comprises administering to the host an immunoprotective dose of the immunogenic composition of the invention is also provided.
  • the vaccine preparations of the present invention may be used to protect or treat a mammal susceptible to infection, by means of administering said vaccine via systemic or mucosal route.
  • These administrations may include injection via the intramuscular, intraperitoneal, intradermal or subcutaneous routes; or via mucosal administration to the oral/alimentary, respiratory, genitourinary tracts.
  • each vaccine dose is selected as an amount which induces an immunoprotective response without significant, adverse side effects in typical vaccines. Such amount will vary depending upon which specific immunogen is employed and how it is presented. Generally, it is expected that each dose will comprise 0.1-100 ⁇ g of polysaccharide, preferably 0.1-50 ⁇ g, preferably 0.1-10 ⁇ g, of which 1 to 5 ⁇ g is the most preferable range.
  • the content of protein antigens in the vaccine will typically be in the range 1-100 ⁇ g, preferably 5-50 ⁇ g, most typically in the range 5 -25 ⁇ g.
  • subjects may receive one or several booster immunisations adequately spaced.
  • Vaccine preparation is generally described in Vaccine Design (“The subunit and adjuvant approach” (eds Powell M. F. & Newman M. J.) (1995) Plenum Press New York). Encapsulation within liposomes is described by Fullerton, U.S. Pat. No. 4,235,877.
  • the inventors have also found that for vaccines comprising TT, DT, Pw and Hib, surprisingly a substantially lower dose of Hib can be used in the combination vaccine (compared with the standard dose of 10 ⁇ g per 0.5 mL dose) to obtain at least equivalent antibody titres against the H. influenzae type b capsular polysaccharide antigen. This is contrary to what would have been expected.
  • a multi-valent immunogenic composition comprising killed whole-cell Bordetella pertussis (Pw), tetanus toxoid (TT), diphtheria toxoid (DT), and a conjugate of a carrier protein and the capsular polysaccharide of H. influenzae type B (Hib—preferably conjugated to TT, DT or CRM197), wherein the amount of conjugate per 0.5 mL dose of bulk vaccine is 1-8 ⁇ g, and the immunogenicity of the conjugate is equivalent or improved over such compositions comprising larger amounts of conjugate.
  • Hepatitis B surface antigen may also be included.
  • the amount of conjugate per 0.5 mL dose of bulk vaccine is less than 10 ⁇ g (of polysaccharide in the conjugate), more preferably 1-7 or 2-6 ⁇ g, and most preferably about 2.5, 3, 4 or 5 ⁇ g.
  • the Hib conjugate is not adsorbed onto aluminium adjuvant salt before being mixed with the DTPw vaccine.
  • combination vaccines comprising a Hib conjugate elicits significantly higher anti-Hib antibody titres in a host (compared with a monovalent, unadsorbed Hib conjugate vaccine) if the Hib conjugate is administered in a vaccine additionally comprising 1, but particularly 2 or more additional bacterial polysaccharides and the Hib polysaccharide (and preferably all the polysaccharides) of the vaccine are not adsorbed onto an adjuvant (particularly aluminium salts).
  • a further, independent, aspect of the invention therefore is the provision of a multi-valent immunogenic composition
  • a multi-valent immunogenic composition comprising a conjugate of a carrier protein and the capsular polysaccharide of H. influenzae type B (Hib), wherein said composition additionally comprises 1, but particularly 2 or more further bacterial polysaccharides (preferably more than 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13) capable of conferring protection to a host against infection by the bacteria from which they are derived, and wherein the Hib polysaccharide (and preferably none of said polysaccharides) in the composition are adsorbed onto an aluminium adjuvant salt. Most preferably there is no aluminium adjuvant salt present in the composition.
  • an antigen not being ‘adsorbed onto an aluminium adjuvant salt’ it is meant that an express or dedicated adsorption step for the antigen on fresh aluminium adjuvant salt is not involved in the process of formulating the composition.
  • Hib may be conjugated to any carrier which can provide at least one T-helper epitope (examples of which are described above), and preferably tetanus toxoid.
  • the further bacterial polysaccharides are also conjugated to a carrier protein (examples of which are described above).
  • the capsular polysaccharide of H. influenzae type B and the further polysaccharides are not conjugated to the same carrier (Hib and none of the further polysaccharides share the same carrier), particularly where the carrier is CRM197.
  • at least one of the polysaccharides of the composition is conjugated onto protein D, however this is not essential for the performance of the invention—indeed neither the Hib nor any of the further polysaccharides need be conjugated onto protein D.
  • Hib and further bacterial polysaccharides (and conjugates thereof) are the only antigens present in the composition.
  • the further bacterial polysaccharides are selected from a group consisting of: N. meningitidis serogroup A capsular polysaccharide (MenA), N. meningitidis serogroup C capsular polysaccharide (MenC), N. meningitidis serogroup Y capsular polysaccharide (MenY), N.
  • meningitidis serogroup W capsular polysaccharide MenW
  • Group B Streptococcus group I capsular polysaccharide Group B Streptococcus group II capsular polysaccharide
  • Group B Streptococcus group III capsular polysaccharide Group B Streptococcus group IV capsular polysaccharide
  • Group B Streptococcus group V capsular polysaccharide Staphylococcus aureus type 5 capsular polysaccharide
  • Staphylococcus aureus type 8 capsular polysaccharide Vi polysaccharide from Salmonella typhi, N. meningitidis LPS, M. catarrhalis LPS, and H.
  • LPS lipo-polysaccharide
  • lipo-oligosaccharide lipo-polysaccharide where the lipid A portion has been detoxified by any of a number of known methods (see for example WO 97/18837 or WO 98/33923), or any molecule comprising the O-polysaccharide derived from said LPS.
  • N. meningitidis LPS it is meant one or more of the 12 known immunotypes (L1, L2, L3, L4, L5, L6, L7, L8, L9, L10, L11 or L12).
  • the amount of PS in each of the above conjugates may be 5 or 10 ⁇ g each per 0.5 mL human dose.
  • the above compositions may also include N. meningitidis serotype B outer membrane vesicles, or one or more N. meningitidis serotype B outer membrane (surface-exposed) proteins, or one or more N. meningitidis LPS (as defined above) to make a global meningitis vaccine.
  • MenA, MenC and MenY are either TT or PD conjugates.
  • the further bacterial polysaccharides may also be selected from any of the capsular pneumococcal polysaccharides (preferably more than 7, more preferably 11 or more, and most preferably 13 or more) such as from serotype: 1, 2, 3, 4, 5, 6A, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F or 33F.
  • the pneumococcal polysaccharides are conjugated (most preferably PD conjugates).
  • pneumococcal polysaccharides derived from at least four serotypes may be selected from the above list. More preferably polysaccharides from more than 7 serotypes are included in the composition, for instance at least 11 serotypes.
  • the composition in one embodiment includes 11 capsular polysaccharides derived from serotypes 1, 3, 4, 5, 6B, 7F, 9V, 14, 18C, 19F and 23F (preferably conjugated).
  • polysaccharide antigens preferably conjugated
  • further polysaccharide antigens for example 23 valent (such as serotypes 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F and 33F), are also contemplated by the invention.
  • serotypes 8 and 12F are advantageously included to form a 13/15 valent vaccine.
  • serotypes 6A and 19A are advantageously included to form a 13 valent vaccine.
  • the pneumococcal polysaccharides may or may not be adsorbed onto aluminium adjuvant salts.
  • GMC post-primary geometric mean concentrations
  • Another indication that no detrimental effect has occurred is if the % of subjects with antibody concentrations of no less than 0.5 ⁇ g/ml differs by no more than 10% (preferably less than 9, 7, 5, 3 or 1%) when comparing 1 month post-primary administrations of the vaccine of the invention versus the vaccine without Hib conjugate.
  • Hib and further bacterial ‘polysaccharides’ the preferred embodiment
  • the invention may be extended to Hib and further bacterial ‘oligosaccharides’ (which naturally have a low number of repeat units, or which are polysaccharides reduced in size for manageability, but are still capable of inducing a protective immune response in a host) which are well known in the vaccine art.
  • the multi-valent immunogenic composition of this aspect of the invention is formulated as a vaccine for in vivo administration to the host wherein the individual components of the composition are formulated such that the immunogenicity of individual components is not impaired by other individual components of the composition (see above definition).
  • the individual components of the composition are formulated such that the immunogenicity of individual components is not impaired by other individual components of the composition (see above definition).
  • no (significantly) detrimental effect occurs to the further bacterial polysaccharides (in terms of protective efficacy) in the combination as compared to their administration in isolation.
  • the multi-valent immunogenic composition of this aspect of the invention is formulated as a vaccine for in vivo administration to the host, which confers an antibody titre superior to the criterion for seroprotection for each antigenic component for an acceptable percentage of human subjects (see above definition).
  • compositions of this aspect of the invention are preferably formulated in a vaccine.
  • the use of the of the multi-valent immunogenic composition of this aspect of the invention in the manufacture of a medicament for the treatment or prevention of diseases caused by infection by Haemophilus influenzae (and preferably also those organisms from which the further bacterial polysaccharides are derived) is also envisioned, as is a method of immunising a human host against disease caused by Haemophilus influenzae (and preferably also those organisms from which the further bacterial polysaccharides are derived), which method comprises administering to the host an immunoprotective dose of the multi-valent immunogenic composition of this aspect of the invention.
  • a process for making the multi-valent immunogenic composition of this aspect of the invention comprising the step of mixing together the individual components. If the further bacterial polysaccharides are to be adsorbed onto an aluminium adjuvant salt, this should be done before Hib is added to the formulation. Preferably an excess of aluminium adjuvant salt should not be used. Most preferably the Hib should be added to the aluminium adjuvanted further polysaccharide extemporanoeusly to the composition being administered to a host.
  • MenAC-Hib N. meningitidis type A capsular polysaccharide conjugated onto protein D (using the CDAP technique), N. meningitidis type C capsular polysaccharide conjugated onto protein D and H. influenzae type b capsular polysaccharide conjugated onto TT were mixed together in an amount of 5 ⁇ g of each polysaccharide in each conjugate per 0.5 mL human dose. The pH was adjusted to 6.1, and was lyophilised in the presence of sucrose.
  • MenC-Hib N. meningitidis type C capsular polysaccharide conjugated onto protein D (using the CDAP technique) and H. influenzae type b capsular polysaccharide conjugated onto TT were mixed together in an amount of 5 ⁇ g of polysaccharide in each conjugate per 0.5 mL human dose. The pH was adjusted to 6.1, and was lyophilised in the presence of sucrose.
  • N. meningitidis type A capsular polysaccharide conjugated onto protein D (using the CDAP techniques), N. meningitidis type C capsular polysaccharide conjugated onto protein D and H. influenzae type b capsular polysaccharide conjugated onto TT were each adsorbed separately in saline onto aluminium phosphate (5 ⁇ g of each conjugate onto 100 ⁇ g, 100 ⁇ g and 60 ⁇ g Al 3+ , respectively, per dose).
  • the adsorbed vaccines were mixed together at a pH of 6.1 and were lyophilised in the presence of sucrose.
  • Study MenAC-Hib 001 evaluates the immunogenicity, reactogenicity and safety induced by MenC-Hib and MenAC-Hib (adsorbed and unadsorbed) made by the above example given as a three-dose primary vaccination in infants.
  • the study was a phase II, randomized study and included five study groups.
  • the formulations that were evaluated were a lyophilized plain and adsorbed formulation of Men AC-Hib and a plain formulation of MenC-Hib. These three formulations were administered to the three first study groups of infants at 3, 4 and 5 months of age; Tritanrix-HepBTM was given concomitantly (as a separate injection) to these three groups.
  • Men AC-Hib The plain formulation of Men AC-Hib was also reconstituted within a liquid diphtheria, tetanus, whole-cell pertussis, hepatitis B combined vaccine (Tritanrix-HepBTM) and administered as a single injection to the fourth study group of infants at 3, 4 and 5 months of age.
  • the fifth group (control) was administered Tritanrix-HepTM-Hib vaccine at 3, 4, 5 months of age.
  • the study was open, but the two first groups receiving the two different formulations of MenAC-Hib were double-blind, as well as the two last groups receiving the Tritanrix-HepBTM-MenAC-Hib and the Tritanrix-HepBTM-Hib vaccines.
  • each formulation that was evaluated induced a good immune response against each antigen (antibodies against meningococcal groups A and C, Poly-Ribosyl-Phosphate (the capsular polysaccharide of H. influenzae type b), Diphtheria toxoid, Tetanus toxoid, Bordetella pertussis and hepatitis B were measured).
  • antigen antigen against meningococcal groups A and C
  • Poly-Ribosyl-Phosphate the capsular polysaccharide of H. influenzae type b
  • Diphtheria toxoid the capsular polysaccharide of H. influenzae type b
  • Tetanus toxoid the capsular polysaccharide of H. influenzae type b
  • Bordetella pertussis Bordetella pertussis and hepatitis B were measured.
  • Each vaccine formulation was well tolerated.
  • This test is an ELISA test that measures IgG content against meningococcal polysaccharide A.
  • FIG. 3 shows the RCC graphs of the data. There is no interference of the MenA polysaccharide antigen to induce at least the same quantity of antibodies when present in a DTPw-HepB/MenAC-Hib vaccine.
  • This test is a bactericidal test that measures the bactericidal antibodies against meningococcus serogroup A. There is no interference of the MenA polysaccharide antigen to induce at least the same quantity of antibodies when present in a DTPw-HepB/MenAC-Hib vaccine.
  • This test is an ELISA test that measures IgG content against meningococcal polysaccharide C.
  • FIG. 4 shows a RCC graph of the data.
  • SBA-MenC is a bactericidal test that measures the bactericidal activity of the serum against meningococcus C. It is a measure of functional antibodies.
  • FIG. 5 shows a RCC graph of the data. There is no interference on the MenC polysaccharide antigen to induce the same quantity of functional antibodies when it is present in a DTPw-HepB/MenAC-Hib vaccine.
  • This test is a bactericidal test that measures the bactericidal antibodies against meningococcus serogroup A. It is a measure of functional antibodies. There is no interference on the MenC polysaccharide antigen to induce the same quantity of functional antibodies when it is present in a DTPw-HepB/MenAC-Hib vaccine. Seroconversion rates of antibodies to diphtheria, tetanus, B.
  • GMT Geometric Mean Titre
  • D T BP HepB MenAC-Hib 2.02 2.18 74.9 357.5 [1.62-2.51] [1.69-2.82] [61.9-90.8] [236.2- 541.2] DTPw-HepB/ 1.69 2.42 71.6 380.2 MenAC-Hib [1.36-2.09] [1.96-3.00] [59.7-85.9] [265.1- 545.2] DTPw-HepB/ 1.26 2.08 69.0 379.1 Hiberix [1.03-1.53] [1.67-2.59] [58.2-81.8] [265.0- 542.2]
  • the pneumococcal vaccine had previously been adsorbed onto 0.5 mg Al 3+ (as AlPO 4 ).
  • Example 4 The vaccine of Example 4 and a control vaccine were administered in a three-dose (3, 4, 5 months of age) schedule to German infants.
  • the immune response results were as follows.
  • Anti pneumococcal IgG antibodies GMC ( ⁇ g/ml) (By Elisa) PS Anti- Group A Group D body Timing N S + [%] GMC N S + [%] GMC Anti-1 PIII 30 100 1.23 33 100 0.99 Anti-3 PIII 30 100 2.04 33 97.0 1.20 Anti-4 PIII 30 100 0.98 33 100 1.03 Anti-5 PIII 30 100 1.33 33 100 1.34 Anti-6B PIII 30 100 0.54 33 100 0.62 Anti-7F PIII 30 100 1.60 33 100 1.33 Anti-9V PIII 30 100 1.61 33 100 1.21 Anti-14 PIII 30 100 2.27 33 100 2.32 Anti-18C PIII 30 100 1.06 33 100 1.04 Anti-19F PIII 30 100 2.05 33 100 1.92 Anti-23F PIII 30 96.7 0.75 33 100 0.76
  • Hiberix (unadsorbed Hib-TT conjugate) has a GMC after a similar administration schedule of about 6 ⁇ g/ml.
  • Group 1 DTPw-HepB extemporaneously mixed with a full dose of Hib-TT (PRP 10 ⁇ g; TT 10-20 ⁇ g; lactose 12.6 ⁇ g; aluminium [as salts] 0.15 mg);
  • Group 2 DTPw-HepB extemporaneously mixed with a half dose of Hib-TT (PRP 5 ⁇ g; TT 10-20 ⁇ g; lactose 10 ⁇ g; aluminium [as salts] 0.0755 mg);
  • Group 3 DTPw-HepB extemporaneously mixed with a quarter dose of Hib-TT (PRP 2.5 ⁇ g; TT 5-10 ⁇ g; lactose 10 ⁇ g; aluminium [as salts] 0.036 mg);
  • Group 4 DTPw-HepB concomitantly administered (in different limbs) with a fill dose of Hib-TT.
  • GTTs Geometric Mean Titers
  • the low dose formulation surprisingly has the highest GMT values. This effect should be even greater if the Hib-TT vaccine is unadsorbed.

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UA76952C2 (uk) 2006-10-16
EP1946769A2 (en) 2008-07-23
JP2010163453A (ja) 2010-07-29
CY1112280T1 (el) 2015-12-09
AU2001281895B2 (en) 2005-04-28
CN1449293A (zh) 2003-10-15
NZ523319A (en) 2006-01-27
CN1449293B (zh) 2012-08-22
EP1946769A3 (en) 2008-07-30
MY133981A (en) 2007-11-30
PL393584A1 (pl) 2011-05-23
WO2002000249A2 (en) 2002-01-03
AU2001281895C1 (en) 2005-10-27
DZ3399A1 (fr) 2002-01-03
EP1296715B2 (en) 2015-12-23
HK1055244A1 (en) 2004-01-02
HU227893B1 (en) 2012-05-29
DK1296715T4 (en) 2016-03-07
NO332495B1 (no) 2012-10-01
HUP0301413A1 (hu) 2003-08-28
BR122012003821B1 (pt) 2020-09-01
JP4870895B2 (ja) 2012-02-08
CA2412497C (en) 2012-10-02
BG66238B1 (bg) 2012-08-31
MA25824A1 (fr) 2003-07-01
PT1946769E (pt) 2012-06-27
HU227613B1 (en) 2011-09-28
BR0112057A (pt) 2003-06-17
HU1000593D0 (en) 2010-12-28
UA85853C2 (uk) 2009-03-10
SK18432002A3 (sk) 2003-08-05
ES2375704T5 (es) 2016-03-03
JP5346308B2 (ja) 2013-11-20
CN101708333A (zh) 2010-05-19
KR20030024714A (ko) 2003-03-26
EA006313B1 (ru) 2005-10-27
AP1695A (en) 2006-12-17
NO20026175L (no) 2003-02-26
PE20020126A1 (es) 2002-04-27
ES2375704T3 (es) 2012-03-05
PL360265A1 (en) 2004-09-06
UY26801A1 (es) 2002-01-31
CY1112915T1 (el) 2016-04-13
HU1000594D0 (en) 2010-12-28
CA2783274C (en) 2018-08-07
PT1296715E (pt) 2012-01-19
SK288007B6 (sk) 2012-10-02
EP1296715A2 (en) 2003-04-02
ATE534402T1 (de) 2011-12-15
BRPI0112057B8 (pt) 2021-05-25
EP1946769B1 (en) 2012-05-30
BG107422A (bg) 2003-09-30
DK1946769T3 (da) 2012-07-16
SI1296715T2 (sl) 2016-03-31
DK1296715T3 (da) 2012-02-13
HUP0301413A3 (en) 2010-01-28
MXPA03000198A (es) 2004-09-13
AU8189501A (en) 2002-01-08
KR100837917B1 (ko) 2008-06-13
US9233151B2 (en) 2016-01-12
KR100898845B1 (ko) 2009-05-21
CZ20024224A3 (cs) 2003-05-14
EP2279748A1 (en) 2011-02-02
IL153506A0 (en) 2003-07-06
IL153506A (en) 2009-06-15
CA2783274A1 (en) 2002-01-03
CA2412497A1 (en) 2002-01-03
US20120207780A1 (en) 2012-08-16
EA200201240A1 (ru) 2003-06-26
PL210015B1 (pl) 2011-11-30
EP2277541A1 (en) 2011-01-26
NO20026175D0 (no) 2002-12-20
HU228384B1 (en) 2013-03-28
SI1296715T1 (sl) 2012-03-30
SI1946769T1 (sl) 2012-07-31
JP2004501873A (ja) 2004-01-22
BRPI0112057B1 (pt) 2016-10-04
OA12302A (en) 2003-10-24

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