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Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys
The latent viral reservoir is the critical barrier for the development of an HIV-1 cure. Previous studies have shown that potent HIV-1 Env-specific broadly neutralizing antibodies (bNAbs) administered at the time of antiretroviral therapy (ART) discontinuation can exert direct antiviral effects, but...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237629/ https://www.ncbi.nlm.nih.gov/pubmed/30283138 http://dx.doi.org/10.1038/s41586-018-0600-6 |
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author | Borducchi, Erica N. Liu, Jinyan Nkolola, Joseph P. Cadena, Anthony M. Yu, Wen-Han Fischinger, Stephanie Broge, Thomas Abbink, Peter Mercado, Noe B. Chandrashekar, Abishek Jetton, David Peter, Lauren McMahan, Katherine Moseley, Edward T. Bekerman, Elena Hesselgesser, Joseph Li, Wenjun Lewis, Mark G. Alter, Galit Geleziunas, Romas Barouch, Dan H. |
author_facet | Borducchi, Erica N. Liu, Jinyan Nkolola, Joseph P. Cadena, Anthony M. Yu, Wen-Han Fischinger, Stephanie Broge, Thomas Abbink, Peter Mercado, Noe B. Chandrashekar, Abishek Jetton, David Peter, Lauren McMahan, Katherine Moseley, Edward T. Bekerman, Elena Hesselgesser, Joseph Li, Wenjun Lewis, Mark G. Alter, Galit Geleziunas, Romas Barouch, Dan H. |
author_sort | Borducchi, Erica N. |
collection | PubMed |
description | The latent viral reservoir is the critical barrier for the development of an HIV-1 cure. Previous studies have shown that potent HIV-1 Env-specific broadly neutralizing antibodies (bNAbs) administered at the time of antiretroviral therapy (ART) discontinuation can exert direct antiviral effects, but whether bNAbs can target the viral reservoir during ART suppression remains unknown. Here we show that the V3 glycan-dependent bNAb PGT121 together with the TLR7 agonist vesatolimod (GS-9620) administered during ART suppression delayed viral rebound following ART discontinuation in SHIV-SF162P3-infected rhesus monkeys that initiated ART during early acute infection. Moreover, the subset of PGT121+GS-9620 treated monkeys that did not show viral rebound following ART discontinuation also did not reveal virus by highly sensitive adoptive transfer and CD8 depletion studies. These data demonstrate the potential of bNAb administration together with innate immune stimulation as a possible strategy to target the viral reservoir. |
format | Online Article Text |
id | pubmed-6237629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-62376292019-04-03 Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys Borducchi, Erica N. Liu, Jinyan Nkolola, Joseph P. Cadena, Anthony M. Yu, Wen-Han Fischinger, Stephanie Broge, Thomas Abbink, Peter Mercado, Noe B. Chandrashekar, Abishek Jetton, David Peter, Lauren McMahan, Katherine Moseley, Edward T. Bekerman, Elena Hesselgesser, Joseph Li, Wenjun Lewis, Mark G. Alter, Galit Geleziunas, Romas Barouch, Dan H. Nature Article The latent viral reservoir is the critical barrier for the development of an HIV-1 cure. Previous studies have shown that potent HIV-1 Env-specific broadly neutralizing antibodies (bNAbs) administered at the time of antiretroviral therapy (ART) discontinuation can exert direct antiviral effects, but whether bNAbs can target the viral reservoir during ART suppression remains unknown. Here we show that the V3 glycan-dependent bNAb PGT121 together with the TLR7 agonist vesatolimod (GS-9620) administered during ART suppression delayed viral rebound following ART discontinuation in SHIV-SF162P3-infected rhesus monkeys that initiated ART during early acute infection. Moreover, the subset of PGT121+GS-9620 treated monkeys that did not show viral rebound following ART discontinuation also did not reveal virus by highly sensitive adoptive transfer and CD8 depletion studies. These data demonstrate the potential of bNAb administration together with innate immune stimulation as a possible strategy to target the viral reservoir. 2018-10-03 2018-11 /pmc/articles/PMC6237629/ /pubmed/30283138 http://dx.doi.org/10.1038/s41586-018-0600-6 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Borducchi, Erica N. Liu, Jinyan Nkolola, Joseph P. Cadena, Anthony M. Yu, Wen-Han Fischinger, Stephanie Broge, Thomas Abbink, Peter Mercado, Noe B. Chandrashekar, Abishek Jetton, David Peter, Lauren McMahan, Katherine Moseley, Edward T. Bekerman, Elena Hesselgesser, Joseph Li, Wenjun Lewis, Mark G. Alter, Galit Geleziunas, Romas Barouch, Dan H. Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys |
title | Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys |
title_full | Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys |
title_fullStr | Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys |
title_full_unstemmed | Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys |
title_short | Antibody and TLR7 Agonist Delay Viral Rebound in SHIV-Infected Monkeys |
title_sort | antibody and tlr7 agonist delay viral rebound in shiv-infected monkeys |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237629/ https://www.ncbi.nlm.nih.gov/pubmed/30283138 http://dx.doi.org/10.1038/s41586-018-0600-6 |
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