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Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties
Compartmentalization of HIV-1 has been observed in the cerebrospinal fluid (CSF) of patients at different clinical stages. Considering the low permeability of the blood-brain barrier, we wondered if a reduced selective pressure by neutralizing antibodies (NAb) in the central nervous system (CNS) cou...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571919/ https://www.ncbi.nlm.nih.gov/pubmed/28841647 http://dx.doi.org/10.1371/journal.pone.0181680 |
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author | Stefic, Karl Chaillon, Antoine Bouvin-Pley, Mélanie Moreau, Alain Braibant, Martine Bastides, Frédéric Gras, Guillaume Bernard, Louis Barin, Francis |
author_facet | Stefic, Karl Chaillon, Antoine Bouvin-Pley, Mélanie Moreau, Alain Braibant, Martine Bastides, Frédéric Gras, Guillaume Bernard, Louis Barin, Francis |
author_sort | Stefic, Karl |
collection | PubMed |
description | Compartmentalization of HIV-1 has been observed in the cerebrospinal fluid (CSF) of patients at different clinical stages. Considering the low permeability of the blood-brain barrier, we wondered if a reduced selective pressure by neutralizing antibodies (NAb) in the central nervous system (CNS) could favor the evolution of NAb-sensitive viruses in this compartment. Single genome amplification (SGA) was used to sequence full-length HIV-1 envelope variants (453 sequences) from paired CSF and blood plasma samples in 9 subjects infected by HIV variants of various clades and suffering from diverse neurologic disorders. Dynamics of viral evolution were evaluated with a bayesian coalescent approach for individuals with longitudinal samples. Pseudotyped viruses expressing envelope glycoproteins variants representative of the quasi-species present in each compartment were generated, and their sensitivity to autologous neutralization, broadly neutralizing antibodies (bNAbs) and entry inhibitors was assessed. Significant compartmentalization of HIV populations between blood and CSF were detected in 5 out of 9 subjects. Some of the previously described genetic determinants for compartmentalization in the CNS were observed regardless of the HIV-1 clade. There was no difference of sensitivity to autologous neutralization between blood- and CSF-variants, even for subjects with compartmentalization, suggesting that selective pressure by autologous NAb is not the main driver of HIV evolution in the CNS. However, we observed major differences of sensitivity to sCD4 or to at least one bNAb targeting either the N160-V1V2 site, the N332-V3 site or the CD4bs, between blood- and CSF-variants in all cases. In particular, HIV-1 variants present in the CSF were more resistant to bNAbs than their blood counterpart in some cases. Considering the possible migration from CSF to blood, the CNS could be a reservoir of bNAb resistant viruses, an observation that should be considered for immunotherapeutic approaches. |
format | Online Article Text |
id | pubmed-5571919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55719192017-09-09 Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties Stefic, Karl Chaillon, Antoine Bouvin-Pley, Mélanie Moreau, Alain Braibant, Martine Bastides, Frédéric Gras, Guillaume Bernard, Louis Barin, Francis PLoS One Research Article Compartmentalization of HIV-1 has been observed in the cerebrospinal fluid (CSF) of patients at different clinical stages. Considering the low permeability of the blood-brain barrier, we wondered if a reduced selective pressure by neutralizing antibodies (NAb) in the central nervous system (CNS) could favor the evolution of NAb-sensitive viruses in this compartment. Single genome amplification (SGA) was used to sequence full-length HIV-1 envelope variants (453 sequences) from paired CSF and blood plasma samples in 9 subjects infected by HIV variants of various clades and suffering from diverse neurologic disorders. Dynamics of viral evolution were evaluated with a bayesian coalescent approach for individuals with longitudinal samples. Pseudotyped viruses expressing envelope glycoproteins variants representative of the quasi-species present in each compartment were generated, and their sensitivity to autologous neutralization, broadly neutralizing antibodies (bNAbs) and entry inhibitors was assessed. Significant compartmentalization of HIV populations between blood and CSF were detected in 5 out of 9 subjects. Some of the previously described genetic determinants for compartmentalization in the CNS were observed regardless of the HIV-1 clade. There was no difference of sensitivity to autologous neutralization between blood- and CSF-variants, even for subjects with compartmentalization, suggesting that selective pressure by autologous NAb is not the main driver of HIV evolution in the CNS. However, we observed major differences of sensitivity to sCD4 or to at least one bNAb targeting either the N160-V1V2 site, the N332-V3 site or the CD4bs, between blood- and CSF-variants in all cases. In particular, HIV-1 variants present in the CSF were more resistant to bNAbs than their blood counterpart in some cases. Considering the possible migration from CSF to blood, the CNS could be a reservoir of bNAb resistant viruses, an observation that should be considered for immunotherapeutic approaches. Public Library of Science 2017-08-25 /pmc/articles/PMC5571919/ /pubmed/28841647 http://dx.doi.org/10.1371/journal.pone.0181680 Text en © 2017 Stefic et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Stefic, Karl Chaillon, Antoine Bouvin-Pley, Mélanie Moreau, Alain Braibant, Martine Bastides, Frédéric Gras, Guillaume Bernard, Louis Barin, Francis Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties |
title | Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties |
title_full | Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties |
title_fullStr | Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties |
title_full_unstemmed | Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties |
title_short | Probing the compartmentalization of HIV-1 in the central nervous system through its neutralization properties |
title_sort | probing the compartmentalization of hiv-1 in the central nervous system through its neutralization properties |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571919/ https://www.ncbi.nlm.nih.gov/pubmed/28841647 http://dx.doi.org/10.1371/journal.pone.0181680 |
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