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                  <mods:namePart>Abad, Raquel</mods:namePart>
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                  <mods:namePart>Biolchi, A</mods:namePart>
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                  <mods:namePart>Moschioni, M</mods:namePart>
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                  <mods:namePart>Giuliani, M M</mods:namePart>
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                  <mods:namePart>Pizza, M</mods:namePart>
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                  <mods:namePart>Vazquez-Moreno, Julio Alberto</mods:namePart>
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               <mods:identifier type="citation">Clin Vaccine Immunol. 2015 Apr;22(4):357-60.</mods:identifier>
               <mods:identifier type="doi">10.1128/CVI.00669-14</mods:identifier>
               <mods:identifier type="e-issn">1556-679X</mods:identifier>
               <mods:identifier type="issn">1556-6811</mods:identifier>
               <mods:identifier type="journal">Clinical and vaccine immunology : CVI</mods:identifier>
               <mods:identifier type="other">https://pmc.ncbi.nlm.nih.gov/articles/PMC4375344/pdf/zcd357.pdf</mods:identifier>
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               <mods:abstract>A new vaccine (the 4CMenB 4-component protein vaccine [Bexsero], which includes PorA, factor H-binding protein [fHbp], neisserial heparin-binding antigen [NHBA], and Neisseria adhesin A [NadA]) against serogroup B meningococci has recently been approved for use in people older than age 2 months in Europe, Australia, and Canada. Preapproval clinical efficacy studies are not feasible for invasive meningococcal disease because its incidence is low/very low, and the serum bactericidal antibody (SBA) titer (or the human SBA [hSBA] titer when human complement is used in the assay) has been used as a surrogate marker of protection. However, the hSBA assay cannot be used on a large scale, and therefore, a meningococcal antigen typing system (MATS) was developed. MATS combines conventional PorA genotyping with an enzyme-linked immunosorbent assay (ELISA) that quantifies both the expression and the cross-reactivity of antigenic variants. The assay has been used to evaluate the potential of the 4CMenB meningococcal group B vaccine to cover group B strains in several countries. Some recent data suggest that MATS is a conservative predictor of strain coverage. We used pooled sera from adolescents and infants to test by the hSBA assay 10 meningococcal group B strains isolated in Spain that were negative for the 3 antigens (n = 9) or that had very low levels of the 3 antigens (n = 1) by MATS. We found that all strains were killed by sera from adolescents and that 5 of the 10 strains were also killed, although at a low titer, by sera from infants. Our data confirm that MATS underestimates vaccine coverage.</mods:abstract>
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                  <mods:title>A large portion of meningococcal antigen typing system-negative meningococcal strains from spain is killed by sera from adolescents and infants immunized with 4CMenB</mods:title>
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