A phase 2 open-label safety and immunogenicity study of a meningococcal B bivalent rLP2086 vaccine in healthy adults

作者：Marshall Helen S^*; Richmond Peter C; Nissen Michael D; Wouters Ann; Baber James; Jiang Qin; Anderson Annaliesa S; Jones Thomas R; Harris Shannon L; Jansen Kathrin U; Perez John L

来源：Vaccine, 2013, 31(12): 1569-1575.

DOI：10.1016/j.vaccine.2013.01.021

• Meningococcal vaccines
• Bacterial outer membrane proteins
• Bactericidal antibodies
• Factor H binding protein
• Serum bactericidal assay
• Neisseria meningitidis serogroup B

Background: Neisseria meningitidis serogroup B (MnB) is a leading cause of bacterial meningitis and septicemia in adolescents and young adults. No currently licensed and available vaccine has been shown to provide broad protection against endemic MnB disease. A bivalent rLP2086 vaccine based on two factor H-binding proteins (fHBPs) has been developed to provide broad protection against MnB disease-causing strains.
Methods: This study assessed the safety and immunogenicity of the final formulation of a bivalent rLP2086 vaccine in 60 healthy adults (18-40 years of age) receiving 120 mu g doses at 0, 1, and 6 months. Safety was assessed by collecting solicited reactogenicity data and participant-reporting of adverse events. Immunogenicity was evaluated by human serum bactericidal assay (hSBA) against 5 MnB strains expressing distinct fHBP variants and fHBP-specific immunoglobulin G titre.
Results: After each immunisation, local reactions such as pain at the injection site and erythema were generally mild or moderate. The most common vaccine-related adverse event was upper respiratory tract infection, which was reported by two participants. Seroprotection (hSBA titres >= 1:4) was achieved in 94.3% of participants against a MnB strain expressing the vaccine-homologous fHBP variant A05 and 70.0%-94.7% against MnB strains expressing the heterologous fHBP variants B02, A22, B44, and B24. Seroconversion rates (>= 4-fold rise in hSBA titres) ranged from 70.0% to 94.7% across the five MnB test strains following the 3-dose vaccination regimen. Immunogenicity responses tended to increase upon subsequent vaccine doses.
Conclusions: Bivalent rLP2086 is a promising vaccine candidate for broad protection against MnB disease-causing strains.

• 出版日期2013-3-15