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Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination

Rapidly evolving RNA viruses, such as the GII.4 strain of human norovirus (HuNoV), and their vaccines elicit complex serological responses associated with previous exposure. Specific correlates of protection, moreover, remain poorly understood. Here, we report the GII.4-serological antibody repertoi...

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Autores principales: Lindesmith, Lisa C., McDaniel, Jonathan R., Changela, Anita, Verardi, Raffaello, Kerr, Scott A., Costantini, Veronica, Brewer-Jensen, Paul D., Mallory, Michael L., Voss, William N., Boutz, Daniel R., Blazeck, John J., Ippolito, Gregory C., Vinje, Jan, Kwong, Peter D., Georgiou, George, Baric, Ralph S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591005/
https://www.ncbi.nlm.nih.gov/pubmed/31216462
http://dx.doi.org/10.1016/j.immuni.2019.05.007
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author Lindesmith, Lisa C.
McDaniel, Jonathan R.
Changela, Anita
Verardi, Raffaello
Kerr, Scott A.
Costantini, Veronica
Brewer-Jensen, Paul D.
Mallory, Michael L.
Voss, William N.
Boutz, Daniel R.
Blazeck, John J.
Ippolito, Gregory C.
Vinje, Jan
Kwong, Peter D.
Georgiou, George
Baric, Ralph S.
author_facet Lindesmith, Lisa C.
McDaniel, Jonathan R.
Changela, Anita
Verardi, Raffaello
Kerr, Scott A.
Costantini, Veronica
Brewer-Jensen, Paul D.
Mallory, Michael L.
Voss, William N.
Boutz, Daniel R.
Blazeck, John J.
Ippolito, Gregory C.
Vinje, Jan
Kwong, Peter D.
Georgiou, George
Baric, Ralph S.
author_sort Lindesmith, Lisa C.
collection PubMed
description Rapidly evolving RNA viruses, such as the GII.4 strain of human norovirus (HuNoV), and their vaccines elicit complex serological responses associated with previous exposure. Specific correlates of protection, moreover, remain poorly understood. Here, we report the GII.4-serological antibody repertoire—pre- and post-vaccination—and select several antibody clonotypes for epitope and structural analysis. The humoral response was dominated by GII.4-specific antibodies that blocked ancestral strains or by antibodies that bound to divergent genotypes and did not block viral-entry-ligand interactions. However, one antibody, A1431, showed broad blockade toward tested GII.4 strains and neutralized the pandemic GII.P16-GII.4 Sydney strain. Structural mapping revealed conserved epitopes, which were occluded on the virion or partially exposed, allowing for broad blockade with neutralizing activity. Overall, our results provide high-resolution molecular information on humoral immune responses after HuNoV vaccination and demonstrate that infection-derived and vaccine-elicited antibodies can exhibit broad blockade and neutralization against this prevalent human pathogen.
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spelling pubmed-65910052019-08-20 Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination Lindesmith, Lisa C. McDaniel, Jonathan R. Changela, Anita Verardi, Raffaello Kerr, Scott A. Costantini, Veronica Brewer-Jensen, Paul D. Mallory, Michael L. Voss, William N. Boutz, Daniel R. Blazeck, John J. Ippolito, Gregory C. Vinje, Jan Kwong, Peter D. Georgiou, George Baric, Ralph S. Immunity Article Rapidly evolving RNA viruses, such as the GII.4 strain of human norovirus (HuNoV), and their vaccines elicit complex serological responses associated with previous exposure. Specific correlates of protection, moreover, remain poorly understood. Here, we report the GII.4-serological antibody repertoire—pre- and post-vaccination—and select several antibody clonotypes for epitope and structural analysis. The humoral response was dominated by GII.4-specific antibodies that blocked ancestral strains or by antibodies that bound to divergent genotypes and did not block viral-entry-ligand interactions. However, one antibody, A1431, showed broad blockade toward tested GII.4 strains and neutralized the pandemic GII.P16-GII.4 Sydney strain. Structural mapping revealed conserved epitopes, which were occluded on the virion or partially exposed, allowing for broad blockade with neutralizing activity. Overall, our results provide high-resolution molecular information on humoral immune responses after HuNoV vaccination and demonstrate that infection-derived and vaccine-elicited antibodies can exhibit broad blockade and neutralization against this prevalent human pathogen. Cell Press 2019-06-18 /pmc/articles/PMC6591005/ /pubmed/31216462 http://dx.doi.org/10.1016/j.immuni.2019.05.007 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lindesmith, Lisa C.
McDaniel, Jonathan R.
Changela, Anita
Verardi, Raffaello
Kerr, Scott A.
Costantini, Veronica
Brewer-Jensen, Paul D.
Mallory, Michael L.
Voss, William N.
Boutz, Daniel R.
Blazeck, John J.
Ippolito, Gregory C.
Vinje, Jan
Kwong, Peter D.
Georgiou, George
Baric, Ralph S.
Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination
title Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination
title_full Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination
title_fullStr Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination
title_full_unstemmed Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination
title_short Sera Antibody Repertoire Analyses Reveal Mechanisms of Broad and Pandemic Strain Neutralizing Responses after Human Norovirus Vaccination
title_sort sera antibody repertoire analyses reveal mechanisms of broad and pandemic strain neutralizing responses after human norovirus vaccination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591005/
https://www.ncbi.nlm.nih.gov/pubmed/31216462
http://dx.doi.org/10.1016/j.immuni.2019.05.007
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