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Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection

Broadly neutralizing antibodies (bnAbs) develop in a subset of HIV-1 infected individuals over 2–3 years of infection. Infected infants develop plasma bnAbs frequently and as early as 1-year post-infection suggesting factors governing bnAb induction in infants are distinct from adults. Understanding...

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Autores principales: Mishra, Nitesh, Sharma, Shaifali, Dobhal, Ayushman, Kumar, Sanjeev, Chawla, Himanshi, Singh, Ravinder, Makhdoomi, Muzamil Ashraf, Das, Bimal Kumar, Lodha, Rakesh, Kabra, Sushil Kumar, Luthra, Kalpana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468291/
https://www.ncbi.nlm.nih.gov/pubmed/32879304
http://dx.doi.org/10.1038/s41467-020-18225-x
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author Mishra, Nitesh
Sharma, Shaifali
Dobhal, Ayushman
Kumar, Sanjeev
Chawla, Himanshi
Singh, Ravinder
Makhdoomi, Muzamil Ashraf
Das, Bimal Kumar
Lodha, Rakesh
Kabra, Sushil Kumar
Luthra, Kalpana
author_facet Mishra, Nitesh
Sharma, Shaifali
Dobhal, Ayushman
Kumar, Sanjeev
Chawla, Himanshi
Singh, Ravinder
Makhdoomi, Muzamil Ashraf
Das, Bimal Kumar
Lodha, Rakesh
Kabra, Sushil Kumar
Luthra, Kalpana
author_sort Mishra, Nitesh
collection PubMed
description Broadly neutralizing antibodies (bnAbs) develop in a subset of HIV-1 infected individuals over 2–3 years of infection. Infected infants develop plasma bnAbs frequently and as early as 1-year post-infection suggesting factors governing bnAb induction in infants are distinct from adults. Understanding viral characteristics in infected infants with early bnAb responses will provide key information about antigenic triggers driving B cell maturation pathways towards induction of bnAbs. Herein, we evaluate the presence of plasma bnAbs in a cohort of 51 HIV-1 clade-C infected infants and identify viral factors associated with early bnAb responses. Plasma bnAbs targeting V2-apex on the env are predominant in infant elite and broad neutralizers. Circulating viral variants in infant elite neutralizers are susceptible to V2-apex bnAbs. In infant elite neutralizers, multivariant infection is associated with plasma bnAbs targeting diverse autologous viruses. Our data provides information supportive of polyvalent vaccination approaches capable of inducing V2-apex bnAbs against HIV-1.
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spelling pubmed-74682912020-09-16 Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection Mishra, Nitesh Sharma, Shaifali Dobhal, Ayushman Kumar, Sanjeev Chawla, Himanshi Singh, Ravinder Makhdoomi, Muzamil Ashraf Das, Bimal Kumar Lodha, Rakesh Kabra, Sushil Kumar Luthra, Kalpana Nat Commun Article Broadly neutralizing antibodies (bnAbs) develop in a subset of HIV-1 infected individuals over 2–3 years of infection. Infected infants develop plasma bnAbs frequently and as early as 1-year post-infection suggesting factors governing bnAb induction in infants are distinct from adults. Understanding viral characteristics in infected infants with early bnAb responses will provide key information about antigenic triggers driving B cell maturation pathways towards induction of bnAbs. Herein, we evaluate the presence of plasma bnAbs in a cohort of 51 HIV-1 clade-C infected infants and identify viral factors associated with early bnAb responses. Plasma bnAbs targeting V2-apex on the env are predominant in infant elite and broad neutralizers. Circulating viral variants in infant elite neutralizers are susceptible to V2-apex bnAbs. In infant elite neutralizers, multivariant infection is associated with plasma bnAbs targeting diverse autologous viruses. Our data provides information supportive of polyvalent vaccination approaches capable of inducing V2-apex bnAbs against HIV-1. Nature Publishing Group UK 2020-09-02 /pmc/articles/PMC7468291/ /pubmed/32879304 http://dx.doi.org/10.1038/s41467-020-18225-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mishra, Nitesh
Sharma, Shaifali
Dobhal, Ayushman
Kumar, Sanjeev
Chawla, Himanshi
Singh, Ravinder
Makhdoomi, Muzamil Ashraf
Das, Bimal Kumar
Lodha, Rakesh
Kabra, Sushil Kumar
Luthra, Kalpana
Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection
title Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection
title_full Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection
title_fullStr Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection
title_full_unstemmed Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection
title_short Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection
title_sort broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant hiv-1 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7468291/
https://www.ncbi.nlm.nih.gov/pubmed/32879304
http://dx.doi.org/10.1038/s41467-020-18225-x
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