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. Author manuscript; available in PMC: 2011 Mar 1.
Published in final edited form as: Clin Infect Dis. 2010 Mar 1;50(S2):S54. doi: 10.1086/648966

Table 1.

Group B vaccines investigated in clinical trials

Formulation Vaccine Clinical Status Immunogenicity Results (humans)
Polysaccharide-protein conjugate N-propionylated group B polysaccharide derivative [22] Phase 1; completed Did not elicit SBA
Detergent-treated OMVs OMV from 1 strain* [2833] Phase 3; completed Elicited SBA and opsonic activity
Mixture of OMV from 2 strains [40, 41] Phase 1; completed Elicited SBA
Mixture of OMV from 2 mutants, each with 3 PorA proteins [4547, 127, 128] Phase 2; completed Elicited SBA
Mixture of OMV from 3 mutants, each with 3 PorA proteins [44] Phase 1 Not yet reported
OMV from Neisseria lactamica [58] Phase 1 Elicited minimal SBA responses
Native OMV (not treated with detergents) Mutant with attenuated endotoxin, 2 PorA proteins, overexpressed fHbp, and other mutations [75] Phase 1 Not yet reported
Recombinant proteins TbpB [92] Phase 1; completed SBA responses not reported
NspA [89] Phase 1; completed Did not elicit SBA
fHbp (2 antigenic variants) [120122] Phase 2 Elicited SBA
2 fusion proteins, GNA 2091-fHbp variant 1 and GNA2132-GNA1030, and Neisseria adhesin A (NadA) [119] (Figure 6) Phase 1 Elicited SBA and opsonic activity
Recombinant proteins + detergent-treated OMV 2 fusion proteins, GNA 2091-fHbp variant 1, and GNA2132-GNA1030, + NadA (Figure 6) + OMV [123, 124] Phase 2/3 Elicited SBA
*

The vaccine from Cuba was combined with group C polysaccharide [30, 31].

Abbreviations used: OMV, outer membrane vesicles; PorA, one of two porin proteins, designated A; fHbp, factor H binding protein; TbpB, transferring-binding protein B; NspA, Neisserial surface protein A; GNA, Genome-derived Neisserial Antigens; NadA, Neisserial adhesin A