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Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection

BACKGROUND: Majority of HIV-1 infection is established by one transmitted/founder virus and understanding how the neutralizing antibodies develop against this virus is critical for our rational design an HIV-1 vaccine. RESULTS: We report here antibody profiling of sequential plasma samples against t...

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Autores principales: Jin, Su, Ji, Yangtao, Wang, Qian, Wang, Hua, Shi, Xuanling, Han, Xiaoxu, Zhou, Tongqing, Shang, Hong, Zhang, Linqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756523/
https://www.ncbi.nlm.nih.gov/pubmed/26883323
http://dx.doi.org/10.1186/s12977-016-0243-3
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author Jin, Su
Ji, Yangtao
Wang, Qian
Wang, Hua
Shi, Xuanling
Han, Xiaoxu
Zhou, Tongqing
Shang, Hong
Zhang, Linqi
author_facet Jin, Su
Ji, Yangtao
Wang, Qian
Wang, Hua
Shi, Xuanling
Han, Xiaoxu
Zhou, Tongqing
Shang, Hong
Zhang, Linqi
author_sort Jin, Su
collection PubMed
description BACKGROUND: Majority of HIV-1 infection is established by one transmitted/founder virus and understanding how the neutralizing antibodies develop against this virus is critical for our rational design an HIV-1 vaccine. RESULTS: We report here antibody profiling of sequential plasma samples against transmitted/founder HIV-1 envelope glycoprotein in an epidemiologically linked transmission pair using our previously reported antigen library approach. We have decomposed the antibody recognition into three major subdomains on the envelope and showed their development in vivo followed a spatiotemporal hierarchy: starting with the ectodomain of gp41 at membrane proximal region, then the V3C3V4 and the V1V2 of gp120 at the membrane distal region. While antibodies to these subdomains appeared to undergo avidity maturation, the early anti-gp41 antibodies failed to translate into detectable autologous neutralization. Instead, it was the much delayed anti-V3C3V4 and anti-V1V2 antibodies constituted the major neutralizing activities. CONCLUSIONS: Our results indicate that the initial antibody response was severely misguided by the transmitted/founder virus and future vaccine design would need to avoid the ectodomain of gp41 and focus on the neutralizing targets in the V3C3V4 and V1V2 subdomains of gp120. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12977-016-0243-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-47565232016-02-18 Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection Jin, Su Ji, Yangtao Wang, Qian Wang, Hua Shi, Xuanling Han, Xiaoxu Zhou, Tongqing Shang, Hong Zhang, Linqi Retrovirology Research BACKGROUND: Majority of HIV-1 infection is established by one transmitted/founder virus and understanding how the neutralizing antibodies develop against this virus is critical for our rational design an HIV-1 vaccine. RESULTS: We report here antibody profiling of sequential plasma samples against transmitted/founder HIV-1 envelope glycoprotein in an epidemiologically linked transmission pair using our previously reported antigen library approach. We have decomposed the antibody recognition into three major subdomains on the envelope and showed their development in vivo followed a spatiotemporal hierarchy: starting with the ectodomain of gp41 at membrane proximal region, then the V3C3V4 and the V1V2 of gp120 at the membrane distal region. While antibodies to these subdomains appeared to undergo avidity maturation, the early anti-gp41 antibodies failed to translate into detectable autologous neutralization. Instead, it was the much delayed anti-V3C3V4 and anti-V1V2 antibodies constituted the major neutralizing activities. CONCLUSIONS: Our results indicate that the initial antibody response was severely misguided by the transmitted/founder virus and future vaccine design would need to avoid the ectodomain of gp41 and focus on the neutralizing targets in the V3C3V4 and V1V2 subdomains of gp120. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12977-016-0243-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-17 /pmc/articles/PMC4756523/ /pubmed/26883323 http://dx.doi.org/10.1186/s12977-016-0243-3 Text en © Jin et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Jin, Su
Ji, Yangtao
Wang, Qian
Wang, Hua
Shi, Xuanling
Han, Xiaoxu
Zhou, Tongqing
Shang, Hong
Zhang, Linqi
Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection
title Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection
title_full Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection
title_fullStr Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection
title_full_unstemmed Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection
title_short Spatiotemporal hierarchy in antibody recognition against transmitted HIV-1 envelope glycoprotein during natural infection
title_sort spatiotemporal hierarchy in antibody recognition against transmitted hiv-1 envelope glycoprotein during natural infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756523/
https://www.ncbi.nlm.nih.gov/pubmed/26883323
http://dx.doi.org/10.1186/s12977-016-0243-3
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