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Toward an Improved Meningococcal Serogroup B Assay

Because of diverse sequences and differential expression of surface structures on individual invasive Neisseria meningitidis serogroup B (MenB) strains, predicting the efficacy of MenB vaccines using traditional human serum bactericidal assays (hSBA) is impractical. The meningococcal antigen surface...

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Detalles Bibliográficos
Autor principal: Poolman, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954221/
https://www.ncbi.nlm.nih.gov/pubmed/29764949
http://dx.doi.org/10.1128/mBio.00713-18
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author Poolman, Jan
author_facet Poolman, Jan
author_sort Poolman, Jan
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description Because of diverse sequences and differential expression of surface structures on individual invasive Neisseria meningitidis serogroup B (MenB) strains, predicting the efficacy of MenB vaccines using traditional human serum bactericidal assays (hSBA) is impractical. The meningococcal antigen surface expression (MEASURE) assay uses flow cytometry to quantitate the expression of factor H binding proteins (fHbp) contained in the bivalent rLP2086 MenB vaccine. To date, experience with MEASURE has been lacking, and in a long-awaited article, McNeil et al. (mBio 9:e00036-18, https://doi.org/10.1128/mBio.00036-18), provide detailed mapping of a cross-reactive antibody binding epitope and explore the potential utility of MEASURE in predicting the susceptibility of individual MenB strains to antibody-mediated killing. Remaining questions center around why some strains with high fHbp expression are nonsusceptible to anti-fHbp antibody killing. Consideration of alternative methods, such as a standardized enzyme-linked immunosorbent assay (ELISA), might offer a more readily available and reproducible assay for wider use.
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spelling pubmed-59542212018-05-23 Toward an Improved Meningococcal Serogroup B Assay Poolman, Jan mBio Commentary Because of diverse sequences and differential expression of surface structures on individual invasive Neisseria meningitidis serogroup B (MenB) strains, predicting the efficacy of MenB vaccines using traditional human serum bactericidal assays (hSBA) is impractical. The meningococcal antigen surface expression (MEASURE) assay uses flow cytometry to quantitate the expression of factor H binding proteins (fHbp) contained in the bivalent rLP2086 MenB vaccine. To date, experience with MEASURE has been lacking, and in a long-awaited article, McNeil et al. (mBio 9:e00036-18, https://doi.org/10.1128/mBio.00036-18), provide detailed mapping of a cross-reactive antibody binding epitope and explore the potential utility of MEASURE in predicting the susceptibility of individual MenB strains to antibody-mediated killing. Remaining questions center around why some strains with high fHbp expression are nonsusceptible to anti-fHbp antibody killing. Consideration of alternative methods, such as a standardized enzyme-linked immunosorbent assay (ELISA), might offer a more readily available and reproducible assay for wider use. American Society for Microbiology 2018-05-15 /pmc/articles/PMC5954221/ /pubmed/29764949 http://dx.doi.org/10.1128/mBio.00713-18 Text en Copyright © 2018 Poolman. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Poolman, Jan
Toward an Improved Meningococcal Serogroup B Assay
title Toward an Improved Meningococcal Serogroup B Assay
title_full Toward an Improved Meningococcal Serogroup B Assay
title_fullStr Toward an Improved Meningococcal Serogroup B Assay
title_full_unstemmed Toward an Improved Meningococcal Serogroup B Assay
title_short Toward an Improved Meningococcal Serogroup B Assay
title_sort toward an improved meningococcal serogroup b assay
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954221/
https://www.ncbi.nlm.nih.gov/pubmed/29764949
http://dx.doi.org/10.1128/mBio.00713-18
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