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The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization
Despite recent progress in engineering native trimeric HIV-1 envelope glycoprotein (Env) mimics as vaccine candidates, Env trimers often induce vaccine-matched neutralizing antibody (NAb) responses. Understanding the specificities of autologous NAb responses and the underlying molecular mechanisms r...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458978/ https://www.ncbi.nlm.nih.gov/pubmed/30970260 http://dx.doi.org/10.1016/j.celrep.2019.03.039 |
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author | Lei, Lin Yang, Yuhe R. Tran, Karen Wang, Yimeng Chiang, Chi-I Ozorowski, Gabriel Xiao, Yongli Ward, Andrew B. Wyatt, Richard T. Li, Yuxing |
author_facet | Lei, Lin Yang, Yuhe R. Tran, Karen Wang, Yimeng Chiang, Chi-I Ozorowski, Gabriel Xiao, Yongli Ward, Andrew B. Wyatt, Richard T. Li, Yuxing |
author_sort | Lei, Lin |
collection | PubMed |
description | Despite recent progress in engineering native trimeric HIV-1 envelope glycoprotein (Env) mimics as vaccine candidates, Env trimers often induce vaccine-matched neutralizing antibody (NAb) responses. Understanding the specificities of autologous NAb responses and the underlying molecular mechanisms restricting the neutralization breadth is therefore informative to improve vaccine efficacy. Here, we delineate the response specificity by single B cell sorting and serum analysis of guinea pigs immunized with BG505 SOSIP.664 Env trimers. Our results reveal a prominent immune target containing both conserved and strain-specific residues in the C3/V4 region of Env in trimer-vaccinated animals. The defined NAb response shares a high degree of similarity with the early NAb response developed by a naturally infected infant from whom the HIV virus strain BG505 was isolated and later developed a broadly NAb response. Our study describes strain-specific responses and their possible evolution pathways, thereby highlighting the potential to broaden NAb responses by immunogen re-design. |
format | Online Article Text |
id | pubmed-6458978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64589782019-04-22 The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization Lei, Lin Yang, Yuhe R. Tran, Karen Wang, Yimeng Chiang, Chi-I Ozorowski, Gabriel Xiao, Yongli Ward, Andrew B. Wyatt, Richard T. Li, Yuxing Cell Rep Article Despite recent progress in engineering native trimeric HIV-1 envelope glycoprotein (Env) mimics as vaccine candidates, Env trimers often induce vaccine-matched neutralizing antibody (NAb) responses. Understanding the specificities of autologous NAb responses and the underlying molecular mechanisms restricting the neutralization breadth is therefore informative to improve vaccine efficacy. Here, we delineate the response specificity by single B cell sorting and serum analysis of guinea pigs immunized with BG505 SOSIP.664 Env trimers. Our results reveal a prominent immune target containing both conserved and strain-specific residues in the C3/V4 region of Env in trimer-vaccinated animals. The defined NAb response shares a high degree of similarity with the early NAb response developed by a naturally infected infant from whom the HIV virus strain BG505 was isolated and later developed a broadly NAb response. Our study describes strain-specific responses and their possible evolution pathways, thereby highlighting the potential to broaden NAb responses by immunogen re-design. Cell Press 2019-04-09 /pmc/articles/PMC6458978/ /pubmed/30970260 http://dx.doi.org/10.1016/j.celrep.2019.03.039 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 Lei, Lin Yang, Yuhe R. Tran, Karen Wang, Yimeng Chiang, Chi-I Ozorowski, Gabriel Xiao, Yongli Ward, Andrew B. Wyatt, Richard T. Li, Yuxing The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization |
title | The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization |
title_full | The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization |
title_fullStr | The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization |
title_full_unstemmed | The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization |
title_short | The HIV-1 Envelope Glycoprotein C3/V4 Region Defines a Prevalent Neutralization Epitope following Immunization |
title_sort | hiv-1 envelope glycoprotein c3/v4 region defines a prevalent neutralization epitope following immunization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458978/ https://www.ncbi.nlm.nih.gov/pubmed/30970260 http://dx.doi.org/10.1016/j.celrep.2019.03.039 |
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