WO2002000249A2

WO2002000249A2 - Multivalent vaccine composition

Info

Publication number: WO2002000249A2
Application number: PCT/EP2001/007288
Authority: WO
Inventors: Dominique Boutriau; Carine Capiau; Pierre Michel Desmons; Dominique Lemoine; Jan Poolman
Original assignee: Glaxosmithkline Biologicals S.A.
Priority date: 2000-06-29
Filing date: 2001-06-27
Publication date: 2002-01-03
Also published as: UA85853C2; EA006313B1; CA2783274A1; DK1296715T3; UA76952C2; DK1946769T3; ATE534402T1; AU2001281895C1; PT1946769E; HUP0301413A1; HK1055244A1; OA12302A; NZ523319A; HUP0301413A3; EG24742A; BR122012003821B1; EP2279748A1; EA200201240A1; EP2277541A1; PL393584A1

Abstract

A multi-valent vaccine composition is described comprising a conjugate of the capsular polysaccharide of H. influenzae b not adsorbed onto an aluminium adjuvant salt, and two or more further bacterial polysaccharides. A multi-valent vaccine composition is also described comprising a whole-cell pertussis component, tetanus toxoid, diphtheria toxoid, Hepatitis B surface antigen, a conjugate of the capsular polysaccharide of H. influenzae b, and a conjugate of a capsular polysaccharide of N. meningitidis type A or C (or both). Furthermore, a multi-valent vaccine composition is described comprising a whole-cell pertussis component, tetanus toxoid, diphtheria toxoid, and a low dose of a conjugate of the capsular polysaccharide of H. influenzae b.

Description

Vaccine Composition

The present invention relates to new combination vaccine formulations. Combination vaccines (which provide protection against multiple pathogens) are very desirable in order to minimise the number of immunisations required to confer protection against multiple pathogens, to lower administration costs, and to increase acceptance and coverage rates. 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 infiuenzae 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 infiuenzae 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 irnmunological performance of any one component of the vaccine.

Accordingly, in one aspect 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 infiuenzae and N. meningitidis comprising:

(a) either killed whole-cell Bordetella pertussis (Pw), or two or more acellular pertussis components (Pa) [preferably the former],

(b) tetanus toxoid (TT),

(c) diphtheria toxoid (DT), (d) Hepatitis B surface antigen (HepB),

(e) a conjugate of a carrier protein and the capsular polysaccharide of H. infiuenzae type B (Hib), and (f) one or more conjugates of a carrier protein and a capsular polysaccharide of a bacterium selected from the group N. meningitidis type A (MenA) and N. meningitidis type C (MenC).

Methods of preparing tetanus toxoid (TT) are well known in the art. For instance, 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 full-length protein (for instance Fragment C - see EP 478602).

Methods of preparing diphtheria toxoid (DT) are also well known in the art. For instance, 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 US 4,709,017, US 5,843,711, US 5,601,827, and US 5,917,017).

Acellular pertussis components (Pa) 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 US 5,085,862).

Methods of preparing killed, whole-cell Bordetella pertussis (Pw) suitable for this invention is disclosed in WO 93/24148, as are suitable formulation methods for producing DT-TT-Pw-HepB and DT-TT-Pa-HepB vaccines. The bacterial capsular polysaccharide conjugates may comprise any carrier peptide, polypeptide or protein comprising at least one T-helper epitope. Preferably the carrier protein(s) used is selected from the group comprising: tetanus toxoid, diphtheria toxoid, CRM197, recombinant diphtheria toxin (as described in any of US 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. infiuenzae (EP 594610). Due to the known effect of carrier suppression, it is advantageous if in each of the compositions of the invention the polysaccharide antigens contained therein ('n' antigens) are conjugated to more than one carrier. Thus (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. For example, in a vaccine containing 4 bacterial polysaccharide conjugates, 1, 2 or all four could be conjugated to different carriers). Protein D, however, 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 infiuenzae. The polysaccharide may be linked to the carrier protein by any known method

(for example, by Likhite, U.S. Patent 4,372,945 and by Armor et al, U.S. Patent 4,474,757). Preferably, CDAP conjugation is carried out (WO 95/08348).

In CDAP, 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 polysaccharides. 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. meningitidis (preferably serotype B) outer membrane (surface-exposed) proteins, killed, attenuated Hepatitis A virus (HepA - preferably the product known as 'Havrix™' [SmithKline Beecham Biologicals]), and inactivated polio virus (IPV - preferably comprising types 1, 2 and 3 as is standard in the vaccine art, most preferably the Salk polio vaccine) without substantial interference problems for any of the antigens of the composition. 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. By not 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.

High levels of Thl-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 Thl 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. In particular, HepB should preferably be adsorbed onto aluminium phosphate before admixing with the other components. In order to minimise the levels of adjuvant (particularly aluminium salts) in the compositions of the invention, 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). Preferably 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.

In a further aspect of the present invention there is provided an immunogenic composition or vaccine as herein described for use in a medicament.

In a still further aspect of the invention there is provided a use of the immunogenic compositions of the invention in the manufacture of a medicament for the treatment or prevention of diseases caused by infection by Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae, Hepatitis B virus, Haemophilus infiuenzae and N. meningitidis.

Additionally, a method of immunising a human host against disease caused by Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae, Hepatitis B virus, Haemophilus infiuenzae 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.

The amount of antigen in 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 μg of polysaccharide, preferably 0.1-50 μg, preferably 0.1-10 μg, of which 1 to 5 μg is the most preferable range. The content of protein antigens in the vaccine will typically be in the range 1- lOOμg, preferably 5-50μg, most typically in the range 5 - 25μg.

Following an initial vaccination, 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, US Patent 4,235,877.

Interestingly, 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 μg per 0.5 mL dose) to obtain at least equivalent antibody titres against the H infiuenzae type b capsular polysaccharide antigen. This is contrary to what would have been expected.

Accordingly, in a further embodiment of the invention there is provided 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. infiuenzae 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 μg, and the immunogenicity of the conjugate is equivalent or improved over such compositions comprising larger amounts of conjugate. Optionally, Hepatitis B surface antigen may also be included.

Preferably the amount of conjugate per 0.5 mL dose of bulk vaccine is less than 10 μg (of polysaccharide in the conjugate), more preferably 1-7 or 2-6 μg, and most preferably about 2.5, 3, 4 or 5 μg. Most preferably the Hib conjugate is not adsorbed onto aluminium adjuvant salt before being mixed with the DTPw vaccine.

A further observation that the inventors have made is the fact that 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 comprising a conjugate of a carrier protein and the capsular polysaccharide of H infiuenzae 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.

By 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.

Preferably, the further bacterial polysaccharides are also conjugated to a carrier protein (examples of which are described above). In specific embodiments the capsular polysaccharide of H. infiuenzae 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. In the preferred embodiments of the examples 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.

In a specific embodiment of the above invention, only Hib and further bacterial polysaccharides (and conjugates thereof) are the only antigens present in the composition.

An amount of polysaccharide which capable of conferring protection to a host (an effective amount) can be readily determined by the skilled person. Generally, it is expected that each dose will comprise 0.1-100 μg of polysaccharide, preferably 0.1-50 μg, preferably 0.1-10 μg, of which 1 to 5 μg is the most preferable range. The Hib conjugate is preferably present in an amount of 3-15 μg (of polysaccharide in the conjugate), more preferably 4-12 μg and most preferably 5-10 μg. In a preferred embodiment a total of no less than 2 μg of further polysaccharide (particularly when conjugated) is present in the composition per 0.5 mL dose, and preferably no less than 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 17, 20, 25, 30, 35, 40, 45 or 50 μg are included. Preferably no more than 100 μg of further polysaccharide are included per 0.5 mL dose.

Preferably 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 infiuenzae LPS. By LPS it is meant either native lipo-polysaccharide (or lipo-oligosaccharide), or 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. By N. meningitidis LPS it is meant one or more of the 12 known immunotypes (LI, L2, L3, L4, L5, L6, L7, L8, L9, L10, LI 1 or L12). Particularly preferred combinations are compositions containing or comprising: 1) conjugated Hib, conjugated MenA and conjugated MenC; 2) conjugated Hib, conjugated MenY and conjugated MenC; and 3) conjugated Hib and conjugated MenC. The amount of PS in each of the above conjugates may be 5 or 10 μg each per 0.5 mL human dose. Optionally, 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. Preferably 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. Preferably the pneumococcal polysaccharides are conjugated (most preferably PD conjugates).

For instance pneumococcal polysaccharides derived from at least four serotypes (including 6B, 14, 19F and 23F for example), or from at least 7 serotypes (including 4, 6B, 9V, 14, 18C, 19F, and 23F for example) 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. For example 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). In a preferred embodiment of the invention at least 13 polysaccharide antigens (preferably conjugated) are included, although further polysaccharide antigens, for example 23 valent (such as serotypes 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11 A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F and 33F), are also contemplated by the invention.

For elderly vaccination (for instance for the prevention of pneumonia) it is advantageous to include serotypes 8 and 12F (and most preferably 15 and 22 as well) to the preferred 11 valent antigenic composition described above to form a 13/15 valent vaccine, whereas for infants or toddlers (where otitis media is of more concern) 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. Hib (preferably lyophilised) and the pneumococcal polysaccharides (preferably in a liquid form) may be mixed extemporaneously before administering to a host in a single administration/injection. With such a formulation it is possible, upon immunisation, to obtain antibody titres against Hib capsular polysaccharide in excess of 100% of the titre obtained when the Hib conjugate is administered in isolation. In preferred embodiments, no (significantly) detrimental effect occurs to the pneumococcal polysaccharide conjugates (in terms of protective efficacy) in the combination as compared to their administration in isolation. This can be assessed in terms of measuring post-primary geometric mean concentrations (GMC) of anti- polysaccharide antibody 1 month after the last primary dose (primary doses being the priming administrations - usually 3 - in the first year of life). The GMC (in μg/ml) for a vaccine of the invention should be preferably over 55% (more preferably over 60, 70, 80, or 90%) of the GMC when the pneumococcal polysaccharides are administered without the Hib conjugate. Another indication that no detrimental effect has occurred is if the % of subjects with antibody concentrations of no less than 0.5 μg/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.

Although the above refers to Hib and further bacterial 'polysaccharides' (the preferred embodiment) it is envisaged that 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.

Preferably, 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). Thus, in preferred embodiments, 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. Preferably, 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). The 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 infiuenzae (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 infiuenzae (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 is also provided, 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. All cited references and publications are incorporated by reference herein.

EXAMPLES Examples are provided solely for the purposes of illustration and are not intended to limit the scope of the invention.

Example 1: Preparation of a DT-TT-Pw-HepB (DTPw-HepB) Vaccine

This was done as described in WO 93/24148. The vaccine is commercially available under the name Tritanrix-HepB™ (SmithKline Beecham Biologicals).

Example 2: Preparation of MenA-MenC-Hib (MenAC-Hib) Vaccines i) Unadjuvanted MenC-Hib or MenA-MenC-Hib

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. infiuenzae type b capsular polysaccharide conjugated onto TT were mixed together in an amount of 5 μg 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. infiuenzae type b capsular polysaccharide conjugated onto TT were mixed together in an amount of 5 μg 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.

ii) Adjuvanted MenA-MenC-Hib 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. infiuenzae type b capsular polysaccharide conjugated onto TT were each adsorbed separately in saline onto aluminium phosphate (5 μg of each conjugate onto 100 μg, 100 μg and 60 μg Al , respectively, per dose). The adsorbed vaccines were mixed together at a pH of 6.1 and were lyophilised in the presence of sucrose.

Example 3: Clinical Trial

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-HepB™ was given concomitantly (as a separate injection) to these three groups. The plain formulation of Men AC-Hib was also reconstituted within a liquid diphtheria, tetanus, whole-cell pertussis, hepatitis B combined vaccine (Tritanrix-HepB™) 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-HepB™-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-HepB™-MenAC-Hib and the Tritanrix-HepB™-Hib vaccines. In summary the study groups were:

Group A MenA_5μgC_5μg-Hib_5μg + DTPw-HepB N=80

Group B MenA₅μgC_5μg-Hib₅μg adsorbed + DTPw-HepB N=80

Group C MenC_5μg-Hib_5μg + DTPw-HepB N=80

Group D DTPw-HepB/MenA₅μ_gC_5μg-Hib5μg N=80

Group E DTPw-HepB/MenA₅μgC_5μg-Hiberix N=80

The results showed that 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 infiuenzae type b), Diphtheria toxoid, Tetanus toxoid, Bordetella pertussis and hepatitis B were measured). Each vaccine formulation was well tolerated.

Post III anti Poly-Ribosyl-Phosphate (PRP)

0.15 and 1.0 mcg/ml are typical titre thresholds which are observed to estimate seroprotection. There is no Hib interference in the DTPw-HepB /MenAC-Hib vaccine. This can also be seen in Fig. 1 which shows the reverse cumulative curve (RCC) of the data. In addition, it is surprising that the non-adsorbed MenAC-Hib vaccine displayed significantly higher anti PRP titre compared with the adsorbed formulation.

Post III anti Protein D IgG

See also Fig. 2 for the respective RCC anti-PD IgG curves. As can be seen, all formulations induced an immune response to the carrier protein (protein D).

Post III anti PSA (capsular polysaccharide of meningococcus A) IgG

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.

Post III anti SBA against meningococcus serogroup A

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. Post III anti PSC (meningococcus C capsular polysaccharide) IgG and SBA-MenC

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.

Post III SBA-MenC against meningococcus serogroup C

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. pertussis cells and HepB

BP refers to B. pertussis. An ELISA test was done measuring IgG against the whole cell bacteria.

Geometric Mean Titre (GMT) of antibodies to diphtheria, tetanus, B. pertussis cells and HepB

From the previous two tables it was observed that the immune response to DT, TT, Pw and HepB are similar to that obtained with the registered Tritanrix-HepB vaccine in terms of both seroconversion and GMT.

Example 4: Preparation of a Hib - 11 valent pneumococcal conjugate (Hib/StrepllV) Vaccine

H. infiuenzae type b capsular polysaccharide conjugated onto TT (10 μg of polysaccharide in the conjugate per dose) which had been lyophilised at a pH of 6.1 in the presence of lactose [Hiberix™ (SmithKline Beecham Biologicals)] was extemporaneously (on the same day as use) dissolved in a liquid solution of eleven- valent pneumococcal capsular polysaccharide (serotypes 1, 3, 4, 5, 6B, 7F, 9V, 14, 18C, 19F and 23F) conjugated onto PD (1 μg of polysaccharide in each conjugate per dose). The pneumococcal vaccine had previously been adsorbed onto 0.5 mg Al³⁺ (as AlPO₄).

Example 5: Clinical Trials on the Vaccine of 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 (measured 1 month after the last primary administration) were as follows.

Anti pneumococcal IgG antibodies: GMC (μg/ml) (ByElisa)

Group A= 1 lPn-PD + Infanrix-HeXa ,TM (Infanrix-Penta plus added Hib conjugate)

TM

Group D = 1 lPn-PD/Hib + Infanrix-PeNTa

+ indicates concomitant (in different limbs) rather than combined administration.

ody concentrations no less than 1.0 μg/ml.

Hiberix (unadsorbed Hib-TT conjugate) has a GMC after a similar administration schedule of about 6 μg/ml.

The immune response, in terms of ELISA antibodies, of infants who received the l lPn-PD/Hib vaccine was similar to that observed for those who received the 1 lPn-PD vaccine for all of the serotypes, with the exception of serotypes 1, 3 and 9V for which a trend to lower geometric mean concentrations was observed for the 1 lPn- PD/Hib vaccine. However, these differences were not significant as shown by the overlapping of 95% confidence intervals. The l lPn-PD/Hib vaccine induced functional (opsonophagocytic) antibodies to all 11 serotypes.

Combining the Hib vaccine with the pneumococcal conjugate vaccine did not significantly interfere with the pneumococcal immune response and surprisingly enhanced the anti PRP response compared to both the registered vaccines Infanrix- HeXa and Hiberix.

Example 6: Clinical Trial on the effect of lower amounts of Hib in a DTPwHepB vaccine

A randomized trial to assess the immunogenicity of a Hib-TT conjugate vaccine at various doses in SB Biologicals DTPwHepB (Tritanrix™-HB) vaccine was carried out as a primary vaccination in healthy infants at 6, 10 and 14 weeks of age. 544 subjects in four groups (136 each) were administered with the following vaccines: Group 1: DTPw-HepB extemporaneously mixed with a full dose of Hib-TT (PRP 10 μg; TT 10-20 μg; lactose 12.6 μg; aluminium [as salts] 0.15 mg); Group 2: DTPw-HepB extemporaneously mixed with a half dose of Hib-TT (PRP 5 μg; TT 10- 20 μg; lactose 10 μg; aluminium [as salts] 0.0755 mg); Group 3: DTPw-HepB extemporaneously mixed with a quarter dose of Hib-TT (PRP 2.5 μg; TT 5-10 μg; lactose 10 μg; aluminium [as salts] 0.036 mg); Group 4: DTPw-HepB concomitantly administered (in different limbs) with a full dose of Hib-TT.

Geometric Mean Titers (GMTs) of anti-PRP antibodies one month after the third dose were as follows:

Group N GMT 95% Conf. Interval

1 130 14.766 11.835 18.423

2 124 17.304 14.209 21.074

3 124 21.010 16.950 26.044

4 126 22.954 18.463 28.538

The low dose formulation surprisingly has the highest GMT values. This effect should be even greater if the Hib-TT vaccine is unadsorbed.

Claims

CLAIMSWe claim:

1. A multi-valent immunogenic composition comprising a conjugate of a carrier protein and the capsular polysaccharide of H. infiuenzae type B, wherein said composition additionally comprises 2 or more further bacterial polysaccharides capable of conferring protection to' a host against infection by the bacteria from which they are derived, and wherein the H infiuenzae type B capsular polysaccharide conjugate is not adsorbed onto an aluminium adjuvant salt.

2. The multi-valent immunogenic composition of claim 1, which comprises more than 7 further bacterial polysaccharides.

3. The multi-valent immunogenic composition of claim 2, wherein the further bacterial polysaccharides are pneumococcal capsular polysaccharides.

4. The multi-valent immunogenic composition of claims 1-3, wherein none of the polysaccharides in the composition are adsorbed onto an aluminium adjuvant salt.

5. The ^' multi-valent immunogenic composition of claims 1-4, wherein the further bacterial polysaccharides are selected from a group consisting of: N. meningitidis serogroup A capsular polysaccharide, N. meningitidis serogroup C capsular polysaccharide, N. meningitidis serogroup Y capsular polysaccharide, N. meningitidis serogroup W capsular polysaccharide, Streptococcus pneumoniae serotype 1 capsular polysaccharide, S. pneumoniae serotype 2 capsular polysaccharide, S. pneumoniae serotype 3 capsular polysaccharide, S. pneumoniae serotype 4 capsular polysaccharide, S. pneumoniae serotype 5 capsular polysaccharide, S. pneumoniae serotype 6A capsular polysaccharide, S. pneumoniae serotype 6B capsular polysaccharide, S. pneumoniae serotype 7F capsular polysaccharide, S. pneumoniae serotype 8 capsular polysaccharide, S. pneumoniae serotype 9N capsular polysaccharide, S. pneumoniae serotype 9V capsular polysaccharide, S. pneumoniae serotype 10A capsular polysaccharide, S. pneumoniae serotype 11A capsular polysaccharide, S. pneumoniae serotype 12F capsular polysaccharide, S. pneumoniae serotype 14 capsular polysaccharide, S. pneumoniae serotype 15B capsular polysaccharide, S. pneumoniae serotype 17F capsular polysaccharide, S. pneumoniae serotype 18C capsular polysaccharide, S. pneumoniae serotype 19A capsular polysaccharide, S. pneumoniae serotype 19F capsular polysaccharide, £. pneumoniae serotype 20 capsular polysaccharide, S. pneumoniae serotype 22F capsular polysaccharide, S. pneumoniae serotype 23F capsular polysaccharide, S. pneumoniae serotype 33F capsular polysaccharide, 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. infiuenzae LPS.

6. The multi-valent immunogenic composition of claims 1-5, wherein the further bacterial polysaccharides are conjugated to a carrier protein.

7. The multi-valent immunogenic composition of claims 1-6, wherein the carrier protein(s) used is selected from the group comprising: tetanus toxoid, diphtheria toxoid, CRM197, recombinant diphtheria toxin, OMPC from N. meningitidis, pneumolysin from S. pneumoniae and protein D from H infiuenzae.

8. The multi-valent immunogenic composition of claim 6 or 7, wherein the capsular polysaccharide of H infiuenzae type B and the further polysaccharides are not conjugated to the same carrier.

9. The multi-valent immunogenic composition of claim 8, wherein the capsular polysaccharide of H. infiuenzae type B and the further polysaccharides are not all conjugated to CRM197.

10. The use of the multi-valent immunogenic composition of claims 1-9 in the manufacture of a medicament for the treatment or prevention of diseases caused by infection by Haemophilus infiuenzae.

11. A method of immunising a human host against disease caused by Haemophilus infiuenzae, which method comprises administering to the host an immunoprotective dose of the multi-valent immunogenic composition of claims 1- 9.

12. 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 infiuenzae and N. meningitidis comprising: a) either killed whole-cell Bordetella pertussis, or two or more acellular pertussis components, b) tetanus toxoid, c) diphtheria toxoid, d) Hepatitis B surface antigen, e) a conjugate of a carrier protein and the capsular polysaccharide of H infiuenzae type B, and f) one or more conjugates of a carrier protein and a capsular polysaccharide of a bacterium selected from the group N. meningitidis type A and _V. meningitidis type C.

13. The immunogenic composition of claim 12 further comprising one or more conjugates of a carrier protein and a capsular polysaccharide of a bacterium selected from the group N. meningitidis type Y and N. meningitidis type W.

14. The immunogenic composition of claim 12 or 13 further comprising killed, attenuated Hepatitis A virus.

15. The immunogenic composition of claims 12-14 further comprising inactivated polio virus.

16. The immunogenic composition of claims 12-15 wherein the carrier protein(s) used is selected from the group comprising: tetanus toxoid, diphtheria toxoid, CRM197, recombinant diphtheria toxin, OMPC from N. meningitidis, and protein D from H. infiuenzae.

17. The immunogenic composition of claims 12-16 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.

18. The immunogenic composition of claims 12-16 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.

19. The immunogenic composition of claims 12-18 further comprising an adjuvant.

20. The immunogenic composition of claim 19 wherein the adjuvant is aluminium salts.

21. The multi-valent immunogenic composition of claims 1-9 and 12-20 for use in a medicament.

22. The use of the immunogenic composition of claims 12-20 in the manufacture of a medicament for the treatment or prevention of diseases caused by infection by Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae, Hepatitis B virus, Haemophilus infiuenzae and N. meningitidis.

23. A method of immunising a human host against disease caused by Bordetella pertussis, Clostridium tetani, Corynebacterium diphtheriae, Hepatitis B virus, Haemophilus infiuenzae and N. meningitidis, which method comprises administering to the host an immunoprotective dose of the immunogenic composition of claims 12-20.

24. A process for making the multi-valent immunogenic composition of claims 1-9 and 12-20 comprising the step of mixing together the individual components.

25. A multi-valent immunogenic composition comprising killed whole-cell Bordetella pertussis, tetanus toxoid, diphtheria toxoid, and a conjugate of a carrier protein and the capsular polysaccharide of H. infiuenzae type B, wherein the amount of conjugate per 0.5 mL dose of bulk vaccine is 1-8 μg, and the immunogenicity of the conjugate is equivalent or improved over such compositions comprising larger amounts of conjugate.

26. The immunogenic composition of claim 25 wherein the carrier protein used is selected from the group comprising: tetanus toxoid, diphtheria toxoid, CRM197,

OMPC from N. meningitidis, and protein D from H infiuenzae.

27. The immunogenic composition of claim 25 or 26 wherein the amount of conjugate per 0.5 mL dose of bulk vaccine is 3-6 μg.

28. The immunogenic composition of claim 25 or 26 wherein the amount of conjugate per 0.5 mL dose of bulk vaccine is 5 μg.

29. The immunogenic composition of claims 25-28, wherein the conjugate of a carrier protein and the capsular polysaccharide of H. infiuenzae type B is not adsorbed onto an aluminium adjuvant salt.