T cell derived HIV-1 is present in the CSF in the face of suppressive antiretroviral therapy
HIV cerebrospinal fluid (CSF) escape, where HIV is suppressed in blood but detectable in CSF, occurs when HIV persists in the CNS despite antiretroviral therapy (ART). To determine the virus producing cell type and whether lowered CSF ART levels are responsible for CSF escape, we collected blood and...
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creator | Lustig, Gila Cele, Sandile Karim, Farina Derache, Anne Ngoepe, Abigail Khan, Khadija Gosnell, Bernadett I Moosa, Mahomed-Yunus S Ntshuba, Ntombi Marais, Suzaan Jeena, Prakash M Govender, Katya Adamson, John Kløverpris, Henrik Gupta, Ravindra K Harrichandparsad, Rohen Patel, Vinod B Sigal, Alex |
description | HIV cerebrospinal fluid (CSF) escape, where HIV is suppressed in blood but detectable in CSF, occurs when HIV persists in the CNS despite antiretroviral therapy (ART). To determine the virus producing cell type and whether lowered CSF ART levels are responsible for CSF escape, we collected blood and CSF from 156 neurosymptomatic participants from Durban, South Africa. We observed that 28% of participants with an undetectable HIV blood viral load showed CSF escape. We detected host cell surface markers on the HIV envelope to determine the cellular source of HIV in participants on the first line regimen of efavirenz, emtricitabine, and tenofovir. We confirmed CD26 as a marker which could differentiate between T cells and macrophages and microglia, and quantified CD26 levels on the virion surface, comparing the result to virus from in vitro infected T cells or macrophages. The measured CD26 level was consistent with the presence of T cell produced virus. We found no significant differences in ART concentrations between CSF escape and fully suppressed individuals in CSF or blood, and did not observe a clear association with drug resistance mutations in CSF virus which would allow HIV to replicate. Hence, CSF HIV in the face of ART may at least partly originate in CD4+ T cell populations. |
doi_str_mv | 10.1371/journal.ppat.1009871 |
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To determine the virus producing cell type and whether lowered CSF ART levels are responsible for CSF escape, we collected blood and CSF from 156 neurosymptomatic participants from Durban, South Africa. We observed that 28% of participants with an undetectable HIV blood viral load showed CSF escape. We detected host cell surface markers on the HIV envelope to determine the cellular source of HIV in participants on the first line regimen of efavirenz, emtricitabine, and tenofovir. We confirmed CD26 as a marker which could differentiate between T cells and macrophages and microglia, and quantified CD26 levels on the virion surface, comparing the result to virus from in vitro infected T cells or macrophages. The measured CD26 level was consistent with the presence of T cell produced virus. We found no significant differences in ART concentrations between CSF escape and fully suppressed individuals in CSF or blood, and did not observe a clear association with drug resistance mutations in CSF virus which would allow HIV to replicate. Hence, CSF HIV in the face of ART may at least partly originate in CD4+ T cell populations.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1009871</identifier><identifier>PMID: 34555123</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Acquired immune deficiency syndrome ; AIDS ; Amino acids ; Antibodies ; Antiretroviral agents ; Antiretroviral drugs ; Antiretroviral therapy ; Biology and Life Sciences ; Blood ; CD4 antigen ; Cell differentiation ; Cell surface ; Cerebrospinal fluid ; Cloning ; Cytotoxicity ; Development and progression ; Dipeptidyl-peptidase IV ; Disease resistance ; Drug resistance ; Drug therapy ; Efavirenz ; Emtricitabine ; Flow cytometry ; Health aspects ; HIV ; HIV infection ; Human immunodeficiency virus ; Infections ; Informed consent ; Laboratories ; Luthuli, A J (Albert John) (1898-1967) ; Lymphocytes ; Lymphocytes T ; Macrophages ; Markers ; Measurement ; Medicine and Health Sciences ; Microglia ; Mutation ; Neurosurgery ; Physiological aspects ; Surface markers ; Surgery ; T cells ; Tenofovir ; Viremia ; Virions ; Viruses</subject><ispartof>PLoS pathogens, 2021-09, Vol.17 (9), p.e1009871-e1009871</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Lustig et al. 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To determine the virus producing cell type and whether lowered CSF ART levels are responsible for CSF escape, we collected blood and CSF from 156 neurosymptomatic participants from Durban, South Africa. We observed that 28% of participants with an undetectable HIV blood viral load showed CSF escape. We detected host cell surface markers on the HIV envelope to determine the cellular source of HIV in participants on the first line regimen of efavirenz, emtricitabine, and tenofovir. We confirmed CD26 as a marker which could differentiate between T cells and macrophages and microglia, and quantified CD26 levels on the virion surface, comparing the result to virus from in vitro infected T cells or macrophages. The measured CD26 level was consistent with the presence of T cell produced virus. We found no significant differences in ART concentrations between CSF escape and fully suppressed individuals in CSF or blood, and did not observe a clear association with drug resistance mutations in CSF virus which would allow HIV to replicate. Hence, CSF HIV in the face of ART may at least partly originate in CD4+ T cell populations.</description><subject>Acquired immune deficiency syndrome</subject><subject>AIDS</subject><subject>Amino acids</subject><subject>Antibodies</subject><subject>Antiretroviral agents</subject><subject>Antiretroviral drugs</subject><subject>Antiretroviral therapy</subject><subject>Biology and Life Sciences</subject><subject>Blood</subject><subject>CD4 antigen</subject><subject>Cell differentiation</subject><subject>Cell surface</subject><subject>Cerebrospinal fluid</subject><subject>Cloning</subject><subject>Cytotoxicity</subject><subject>Development and progression</subject><subject>Dipeptidyl-peptidase IV</subject><subject>Disease resistance</subject><subject>Drug resistance</subject><subject>Drug therapy</subject><subject>Efavirenz</subject><subject>Emtricitabine</subject><subject>Flow cytometry</subject><subject>Health aspects</subject><subject>HIV</subject><subject>HIV infection</subject><subject>Human immunodeficiency virus</subject><subject>Infections</subject><subject>Informed consent</subject><subject>Laboratories</subject><subject>Luthuli, A J (Albert John) (1898-1967)</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Macrophages</subject><subject>Markers</subject><subject>Measurement</subject><subject>Medicine and Health Sciences</subject><subject>Microglia</subject><subject>Mutation</subject><subject>Neurosurgery</subject><subject>Physiological aspects</subject><subject>Surface markers</subject><subject>Surgery</subject><subject>T 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cell derived HIV-1 is present in the CSF in the face of suppressive antiretroviral therapy</title><author>Lustig, Gila ; Cele, Sandile ; Karim, Farina ; Derache, Anne ; Ngoepe, Abigail ; Khan, Khadija ; Gosnell, Bernadett I ; Moosa, Mahomed-Yunus S ; Ntshuba, Ntombi ; Marais, Suzaan ; Jeena, Prakash M ; Govender, Katya ; Adamson, John ; Kløverpris, Henrik ; Gupta, Ravindra K ; Harrichandparsad, Rohen ; Patel, Vinod B ; Sigal, Alex</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c638t-62cda45037f34e9850d06cd4e637ff258300c2d0519fcae394fdfbbb3b76cd953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acquired immune deficiency syndrome</topic><topic>AIDS</topic><topic>Amino acids</topic><topic>Antibodies</topic><topic>Antiretroviral agents</topic><topic>Antiretroviral drugs</topic><topic>Antiretroviral therapy</topic><topic>Biology and Life Sciences</topic><topic>Blood</topic><topic>CD4 antigen</topic><topic>Cell differentiation</topic><topic>Cell surface</topic><topic>Cerebrospinal fluid</topic><topic>Cloning</topic><topic>Cytotoxicity</topic><topic>Development and progression</topic><topic>Dipeptidyl-peptidase IV</topic><topic>Disease resistance</topic><topic>Drug resistance</topic><topic>Drug therapy</topic><topic>Efavirenz</topic><topic>Emtricitabine</topic><topic>Flow cytometry</topic><topic>Health aspects</topic><topic>HIV</topic><topic>HIV infection</topic><topic>Human immunodeficiency virus</topic><topic>Infections</topic><topic>Informed consent</topic><topic>Laboratories</topic><topic>Luthuli, A J (Albert John) (1898-1967)</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Macrophages</topic><topic>Markers</topic><topic>Measurement</topic><topic>Medicine and Health Sciences</topic><topic>Microglia</topic><topic>Mutation</topic><topic>Neurosurgery</topic><topic>Physiological 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B</au><au>Sigal, Alex</au><au>Swanstrom, Ronald</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>T cell derived HIV-1 is present in the CSF in the face of suppressive antiretroviral therapy</atitle><jtitle>PLoS pathogens</jtitle><date>2021-09-23</date><risdate>2021</risdate><volume>17</volume><issue>9</issue><spage>e1009871</spage><epage>e1009871</epage><pages>e1009871-e1009871</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>HIV cerebrospinal fluid (CSF) escape, where HIV is suppressed in blood but detectable in CSF, occurs when HIV persists in the CNS despite antiretroviral therapy (ART). To determine the virus producing cell type and whether lowered CSF ART levels are responsible for CSF escape, we collected blood and CSF from 156 neurosymptomatic participants from Durban, South Africa. We observed that 28% of participants with an undetectable HIV blood viral load showed CSF escape. We detected host cell surface markers on the HIV envelope to determine the cellular source of HIV in participants on the first line regimen of efavirenz, emtricitabine, and tenofovir. We confirmed CD26 as a marker which could differentiate between T cells and macrophages and microglia, and quantified CD26 levels on the virion surface, comparing the result to virus from in vitro infected T cells or macrophages. The measured CD26 level was consistent with the presence of T cell produced virus. We found no significant differences in ART concentrations between CSF escape and fully suppressed individuals in CSF or blood, and did not observe a clear association with drug resistance mutations in CSF virus which would allow HIV to replicate. Hence, CSF HIV in the face of ART may at least partly originate in CD4+ T cell populations.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>34555123</pmid><doi>10.1371/journal.ppat.1009871</doi><orcidid>https://orcid.org/0000-0002-0905-7164</orcidid><orcidid>https://orcid.org/0000-0001-9698-016X</orcidid><orcidid>https://orcid.org/0000-0002-8204-0182</orcidid><orcidid>https://orcid.org/0000-0001-9751-1808</orcidid><orcidid>https://orcid.org/0000-0002-0391-8496</orcidid><orcidid>https://orcid.org/0000-0001-8571-2004</orcidid><orcidid>https://orcid.org/0000-0001-6191-4023</orcidid><orcidid>https://orcid.org/0000-0001-5753-0107</orcidid><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Public Library of Science (PLoS) Journals Open Access; PubMed Central |
subjects | Acquired immune deficiency syndrome AIDS Amino acids Antibodies Antiretroviral agents Antiretroviral drugs Antiretroviral therapy Biology and Life Sciences Blood CD4 antigen Cell differentiation Cell surface Cerebrospinal fluid Cloning Cytotoxicity Development and progression Dipeptidyl-peptidase IV Disease resistance Drug resistance Drug therapy Efavirenz Emtricitabine Flow cytometry Health aspects HIV HIV infection Human immunodeficiency virus Infections Informed consent Laboratories Luthuli, A J (Albert John) (1898-1967) Lymphocytes Lymphocytes T Macrophages Markers Measurement Medicine and Health Sciences Microglia Mutation Neurosurgery Physiological aspects Surface markers Surgery T cells Tenofovir Viremia Virions Viruses |
title | T cell derived HIV-1 is present in the CSF in the face of suppressive antiretroviral therapy |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T22%3A33%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=T%20cell%20derived%20HIV-1%20is%20present%20in%20the%20CSF%20in%20the%20face%20of%20suppressive%20antiretroviral%20therapy&rft.jtitle=PLoS%20pathogens&rft.au=Lustig,%20Gila&rft.date=2021-09-23&rft.volume=17&rft.issue=9&rft.spage=e1009871&rft.epage=e1009871&rft.pages=e1009871-e1009871&rft.issn=1553-7374&rft.eissn=1553-7374&rft_id=info:doi/10.1371/journal.ppat.1009871&rft_dat=%3Cgale_plos_%3EA677503073%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2582586178&rft_id=info:pmid/34555123&rft_galeid=A677503073&rft_doaj_id=oai_doaj_org_article_a1fcfa49647c48ec8249fe5457393dfd&rfr_iscdi=true |