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dc.contributor.authorDiNapoli, Sarah R.
dc.contributor.authorOrtiz, Alexandra M.
dc.contributor.authorWu, Fan
dc.contributor.authorMatsuda, Kenta
dc.contributor.authorTwigg, Homer L.
dc.contributor.authorHirsch, Vanessa M.
dc.contributor.authorKnox, Kenneth
dc.contributor.authorBrenchley, Jason M.
dc.date.accessioned2017-05-04T20:20:05Z
dc.date.available2017-05-04T20:20:05Z
dc.date.issued2017-02-23
dc.identifier.citationTissue-resident macrophages can contain replication-competent virus in antiretroviral-naive, SIV-infected Asian macaques 2017, 2 (4) JCI Insighten
dc.identifier.issn2379-3708
dc.identifier.pmid28239657
dc.identifier.doi10.1172/jci.insight.91214
dc.identifier.urihttp://hdl.handle.net/10150/623383
dc.description.abstractSIV DNA can be detected in lymphoid tissue-resident macrophages of chronically SIV-infected Asian macaques. These macrophages also contain evidence of recently phagocytosed SIV-infected CD4(+) T cells. Here, we examine whether these macrophages contain replication-competent virus, whether viral DNA can be detected in tissue-resident macrophages from antiretroviral (ARV) therapy-treated animals and humans, and how the viral sequences amplified from macrophages and contemporaneous CD4(+) T cells compare. In ARV-naive animals, we find that lymphoid tissue-resident macrophages contain replication-competent virus if they also contain viral DNA in ARV-naive Asian macaques. The genetic sequence of the virus within these macrophages is similar to those within CD4(+) T cells from the same anatomic sites. In ARV-treated animals, we find that viral DNA can be amplified from lymphoid tissue-resident macrophages of SIV-infected Asian macaques that were treated with ARVs for at least 5 months, but we could not detect replicationcompetent virus from macrophages of animals treated with ARVs. Finally, we could not detect viral DNA in alveolar macrophages from HIV-infected individuals who received ARVs for 3 years and had undetectable viral loads. These data demonstrate that macrophages can contain replicationcompetent virus, but may not represent a significant reservoir for HIV in vivo.
dc.description.sponsorshipDivision of Intramural Research/NIAID/NIHen
dc.language.isoenen
dc.publisherAMER SOC CLINICAL INVESTIGATION INCen
dc.relation.urlhttps://insight.jci.org/articles/view/91214en
dc.rightsCopyright © 2017, American Society for Clinical Investigation.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.titleTissue-resident macrophages can contain replication-competent virus in antiretroviral-naive, SIV-infected Asian macaquesen
dc.typeArticleen
dc.contributor.departmentUniv Arizona, Dept Meden
dc.identifier.journalJCI Insighten
dc.description.noteAuthors can deposit to institutional repositories, and we request that they deposit the final, published JCI Insight version.en
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en
dc.eprint.versionFinal published versionen
dc.internal.reviewer-noteConfirming publisher policy.en
refterms.dateFOA2018-08-15T17:11:58Z
html.description.abstractSIV DNA can be detected in lymphoid tissue-resident macrophages of chronically SIV-infected Asian macaques. These macrophages also contain evidence of recently phagocytosed SIV-infected CD4(+) T cells. Here, we examine whether these macrophages contain replication-competent virus, whether viral DNA can be detected in tissue-resident macrophages from antiretroviral (ARV) therapy-treated animals and humans, and how the viral sequences amplified from macrophages and contemporaneous CD4(+) T cells compare. In ARV-naive animals, we find that lymphoid tissue-resident macrophages contain replication-competent virus if they also contain viral DNA in ARV-naive Asian macaques. The genetic sequence of the virus within these macrophages is similar to those within CD4(+) T cells from the same anatomic sites. In ARV-treated animals, we find that viral DNA can be amplified from lymphoid tissue-resident macrophages of SIV-infected Asian macaques that were treated with ARVs for at least 5 months, but we could not detect replicationcompetent virus from macrophages of animals treated with ARVs. Finally, we could not detect viral DNA in alveolar macrophages from HIV-infected individuals who received ARVs for 3 years and had undetectable viral loads. These data demonstrate that macrophages can contain replicationcompetent virus, but may not represent a significant reservoir for HIV in vivo.


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