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ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection

Despite antibody-dependent cellular cytotoxicity (ADCC) responses being implicated in protection from HIV-1 infection, there is limited evidence that they control virus replication. The high mutability of HIV-1 enables the virus to rapidly adapt, and thus evidence of viral escape is a very sensitive...

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Autores principales: Mielke, Dieter, Bandawe, Gama, Zheng, Jie, Jones, Jennifer, Abrahams, Melissa-Rose, Bekker, Valerie, Ochsenbauer, Christina, Garrett, Nigel, Abdool Karim, Salim, Moore, Penny L., Morris, Lynn, Montefiori, David, Anthony, Colin, Ferrari, Guido, Williamson, Carolyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598021/
https://www.ncbi.nlm.nih.gov/pubmed/34788337
http://dx.doi.org/10.1371/journal.ppat.1010046
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author Mielke, Dieter
Bandawe, Gama
Zheng, Jie
Jones, Jennifer
Abrahams, Melissa-Rose
Bekker, Valerie
Ochsenbauer, Christina
Garrett, Nigel
Abdool Karim, Salim
Moore, Penny L.
Morris, Lynn
Montefiori, David
Anthony, Colin
Ferrari, Guido
Williamson, Carolyn
author_facet Mielke, Dieter
Bandawe, Gama
Zheng, Jie
Jones, Jennifer
Abrahams, Melissa-Rose
Bekker, Valerie
Ochsenbauer, Christina
Garrett, Nigel
Abdool Karim, Salim
Moore, Penny L.
Morris, Lynn
Montefiori, David
Anthony, Colin
Ferrari, Guido
Williamson, Carolyn
author_sort Mielke, Dieter
collection PubMed
description Despite antibody-dependent cellular cytotoxicity (ADCC) responses being implicated in protection from HIV-1 infection, there is limited evidence that they control virus replication. The high mutability of HIV-1 enables the virus to rapidly adapt, and thus evidence of viral escape is a very sensitive approach to demonstrate the importance of this response. To enable us to deconvolute ADCC escape from neutralizing antibody (nAb) escape, we identified individuals soon after infection with detectable ADCC responses, but no nAb responses. We evaluated the kinetics of ADCC and nAb responses, and viral escape, in five recently HIV-1-infected individuals. In one individual we detected viruses that escaped from ADCC responses but were sensitive to nAbs. In the remaining four participants, we did not find evidence of viral evolution exclusively associated with ADCC-mediating non-neutralizing Abs (nnAbs). However, in all individuals escape from nAbs was rapid, occurred at very low titers, and in three of five cases we found evidence of viral escape before detectable nAb responses. These data show that ADCC-mediating nnAbs can drive immune escape in early infection, but that nAbs were far more effective. This suggests that if ADCC responses have a protective role, their impact is limited after systemic virus dissemination.
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spelling pubmed-85980212021-11-18 ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection Mielke, Dieter Bandawe, Gama Zheng, Jie Jones, Jennifer Abrahams, Melissa-Rose Bekker, Valerie Ochsenbauer, Christina Garrett, Nigel Abdool Karim, Salim Moore, Penny L. Morris, Lynn Montefiori, David Anthony, Colin Ferrari, Guido Williamson, Carolyn PLoS Pathog Research Article Despite antibody-dependent cellular cytotoxicity (ADCC) responses being implicated in protection from HIV-1 infection, there is limited evidence that they control virus replication. The high mutability of HIV-1 enables the virus to rapidly adapt, and thus evidence of viral escape is a very sensitive approach to demonstrate the importance of this response. To enable us to deconvolute ADCC escape from neutralizing antibody (nAb) escape, we identified individuals soon after infection with detectable ADCC responses, but no nAb responses. We evaluated the kinetics of ADCC and nAb responses, and viral escape, in five recently HIV-1-infected individuals. In one individual we detected viruses that escaped from ADCC responses but were sensitive to nAbs. In the remaining four participants, we did not find evidence of viral evolution exclusively associated with ADCC-mediating non-neutralizing Abs (nnAbs). However, in all individuals escape from nAbs was rapid, occurred at very low titers, and in three of five cases we found evidence of viral escape before detectable nAb responses. These data show that ADCC-mediating nnAbs can drive immune escape in early infection, but that nAbs were far more effective. This suggests that if ADCC responses have a protective role, their impact is limited after systemic virus dissemination. Public Library of Science 2021-11-17 /pmc/articles/PMC8598021/ /pubmed/34788337 http://dx.doi.org/10.1371/journal.ppat.1010046 Text en © 2021 Mielke et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mielke, Dieter
Bandawe, Gama
Zheng, Jie
Jones, Jennifer
Abrahams, Melissa-Rose
Bekker, Valerie
Ochsenbauer, Christina
Garrett, Nigel
Abdool Karim, Salim
Moore, Penny L.
Morris, Lynn
Montefiori, David
Anthony, Colin
Ferrari, Guido
Williamson, Carolyn
ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection
title ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection
title_full ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection
title_fullStr ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection
title_full_unstemmed ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection
title_short ADCC-mediating non-neutralizing antibodies can exert immune pressure in early HIV-1 infection
title_sort adcc-mediating non-neutralizing antibodies can exert immune pressure in early hiv-1 infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598021/
https://www.ncbi.nlm.nih.gov/pubmed/34788337
http://dx.doi.org/10.1371/journal.ppat.1010046
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