Abstract
BackgroundSerogroup B meningococcal (MenB) isolates currently account for approximately 90% of invasive meningococcal disease (IMD) in Greece with ST-162 clonal complex predominating. The potential of a multicomponent meningococcal B vaccine (4CMenB) recently licensed in Europe was investigated in order to find whether the aforementioned vaccine will cover the MenB strains circulating in Greece. A panel of 148 serogroup B invasive meningococcal strains was characterized by multilocus sequence typing (MLST) and PorA subtyping. Vaccine components were typed by sequencing for factor H-binding protein (fHbp), Neisserial Heparin Binding Antigen (NHBA) and Neisseria adhesin A (NadA). Their expression was explored by Meningococcal Antigen Typing System (MATS).ResultsGlobal strain coverage predicted by MATS was 89.2% (95% CI 63.5%-98.6%) with 44.6%, 38.5% and 6.1% of strains covered by one, two and three vaccine antigens respectively. NHBA was the antigen responsible for the highest coverage (78.4%), followed by fHbp (52.7%), PorA (8.1%) and NadA (0.7%). The coverage of the major genotypes did not differ significantly. The most prevalent MLST genotype was the ST-162 clonal complex , accounting for 44.6% of the strains in the panel and with a predicted coverage of 86.4%, mainly due to NHBA and fHbp.Conclusions4CMenB has the potential to protect against a significant proportion of Greek invasive MenB strains.
Highlights
Serogroup B meningococcal (MenB) isolates currently account for approximately 90% of invasive meningococcal disease (IMD) in Greece with sequence types (STs)-162 clonal complex predominating
A novel multicomponent vaccine against invasive disease caused by meningococcal capsular group B (MenB), 4CMenB (Bexsero®), containing four major components: factor H-binding protein [7], Neisserial Heparin Binding Antigen (NHBA) [8], Neisseria Adhesin A (NadA)
For vaccines based on meningococcal serogroups A, C, W and Y capsular polysaccharide conjugates which have been licensed in many parts of the world [11,12,13], the immunogenicity has been evaluated by means of complement–mediated killing using the serum bactericidal assay (SBA) of 4 strains belonging to each serogroup and the coverage is estimated on the basis of the epidemiological serogroup distribution [14,15,16]
Summary
Serogroup B meningococcal (MenB) isolates currently account for approximately 90% of invasive meningococcal disease (IMD) in Greece with ST-162 clonal complex predominating. A novel multicomponent vaccine against invasive disease caused by meningococcal capsular group B (MenB), 4CMenB (Bexsero®), containing four major components: factor H-binding protein (fHbp) [7], Neisserial Heparin Binding Antigen (NHBA) [8], Neisseria Adhesin A (NadA). For vaccines based on meningococcal serogroups A, C, W and Y capsular polysaccharide conjugates which have been licensed in many parts of the world [11,12,13], the immunogenicity has been evaluated by means of complement–mediated killing using the serum bactericidal assay (SBA) of 4 strains belonging to each serogroup and the coverage is estimated on the basis of the epidemiological serogroup distribution [14,15,16] This is very difficult for the evaluation of the novel recombinant protein-vaccine that aimed to target serogroup B due to the fact that the protein antigens may vary in their sequence and level of expression across strains [17]. Alternative means of measuring the probability of killing in the hSBA by antibodies induced by the surface protein based vaccine are necessary [18]
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