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dc.contributor.authorDi Mascio, Michele
dc.contributor.authorSrinivasula, Sharat
dc.contributor.authorKim, Insook
dc.contributor.authorDuralde, Gorka
dc.contributor.authorSt. Claire, Alexis
dc.contributor.authorDeGrange, Paula
dc.contributor.authorSt. Claire, Marisa
dc.contributor.authorReimann, Keith A.
dc.contributor.authorGabriel, Erin E.
dc.contributor.authorCarrasquillo, Jorge
dc.contributor.authorReba, Richard C.
dc.contributor.authorPaik, Chang
dc.contributor.authorLane, Henry C.
dc.date2022-08-11T08:09:50.000
dc.date.accessioned2022-08-23T16:45:39Z
dc.date.available2022-08-23T16:45:39Z
dc.date.issued2018-07-12
dc.date.submitted2018-09-12
dc.identifier.citation<p>JCI Insight. 2018 Jul 12;3(13). pii: 97880. doi: 10.1172/jci.insight.97880. [Epub ahead of print] <a href="https://doi.org/10.1172/jci.insight.97880">Link to article on publisher's site</a></p>
dc.identifier.issn2379-3708 (Linking)
dc.identifier.doi10.1172/jci.insight.97880
dc.identifier.pmid29997291
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40724
dc.description.abstractThe peripheral blood represents only a small fraction of the total number of lymphocytes in the body. To develop a more thorough understanding of T cell dynamics, including the effects of SIV/SHIV/HIV infection on immune cell depletion and immune reconstitution following combination antiretroviral therapy (cART), one needs to utilize approaches that allow direct visualization of lymphoid tissues. In the present study, noninvasive in vivo imaging of the CD4+ T cell pool has revealed that the timing of the CD4+ T cell pool reconstitution following initiation of ART in SIV-infected nonhuman primates (NHPs) appears seemingly stochastic among clusters of lymph nodes within the same host. At 4 weeks following initiation or interruption of cART, the changes observed in peripheral blood (PB) are primarily related to changes in the whole-body CD4 pool rather than changes in lymphocyte trafficking. Lymph node CD4 pools in long-term antiretroviral-treated and plasma viral load-suppressed hosts appear suboptimally reconstituted compared with healthy controls, while splenic CD4 pools appear similar between the 2 groups.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=29997291&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright © 2018, American Society for Clinical Investigation. The JCI is an open access journal. Publisher PDF posted as allowed by the publisher's policy posted at https://www.jci.org/kiosks/terms.
dc.subjectAIDS/HIV
dc.subjectDiagnostic imaging
dc.subjectImmunology
dc.subjectImmunity
dc.subjectImmunology of Infectious Disease
dc.subjectImmunoprophylaxis and Therapy
dc.subjectVirus Diseases
dc.titleTotal body CD4+ T cell dynamics in treated and untreated SIV infection revealed by in vivo imaging
dc.typeJournal Article
dc.source.journaltitleJCI insight
dc.source.volume3
dc.source.issue13
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4540&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3528
dc.identifier.contextkey12829022
refterms.dateFOA2022-08-23T16:45:39Z
html.description.abstract<p>The peripheral blood represents only a small fraction of the total number of lymphocytes in the body. To develop a more thorough understanding of T cell dynamics, including the effects of SIV/SHIV/HIV infection on immune cell depletion and immune reconstitution following combination antiretroviral therapy (cART), one needs to utilize approaches that allow direct visualization of lymphoid tissues. In the present study, noninvasive in vivo imaging of the CD4+ T cell pool has revealed that the timing of the CD4+ T cell pool reconstitution following initiation of ART in SIV-infected nonhuman primates (NHPs) appears seemingly stochastic among clusters of lymph nodes within the same host. At 4 weeks following initiation or interruption of cART, the changes observed in peripheral blood (PB) are primarily related to changes in the whole-body CD4 pool rather than changes in lymphocyte trafficking. Lymph node CD4 pools in long-term antiretroviral-treated and plasma viral load-suppressed hosts appear suboptimally reconstituted compared with healthy controls, while splenic CD4 pools appear similar between the 2 groups.</p>
dc.identifier.submissionpathoapubs/3528
dc.contributor.departmentMassBiologics
dc.source.pagese97880


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