Both CD31 super(+) and CD31 super(-) Naive CD4 super(+) T Cells Are Persistent HIV Type 1-Infected Reservoirs in Individuals Receiving Antiretroviral Therapy

Background. Naive T cell recovery is critical for successful immune reconstitution after antiretroviral therapy (ART), but the relative contribution of CD31 super(+) and CD31 super(-) naive T cells to immune reconstitution and viral persistence is unknown. Methods. In a cross-sectional (n[inline ima...

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Published inThe Journal of infectious diseases Vol. 202; no. 11; pp. 1738 - 1748
Main Authors Wightman, Fiona, Solomon, Ajantha, Khoury, Gabriela, Green, Justin A, Gray, Lachlan, Gorry, Paul R, Ho, Yung Shwen, Saksena, Nitin K, Hoy, Jennifer, Crowe, Suzanne M, Cameron, Paul U, Lewin, Sharon R
Format Journal Article
LanguageEnglish
Published 01.01.2010
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Summary:Background. Naive T cell recovery is critical for successful immune reconstitution after antiretroviral therapy (ART), but the relative contribution of CD31 super(+) and CD31 super(-) naive T cells to immune reconstitution and viral persistence is unknown. Methods. In a cross-sectional (n[inline image]=[inline image]94) and longitudinal (n[inline image]=[inline image]10) study of human immunodeficiency virus (HIV)-infected patients before and after ART, we examined the ratio of CD31 super(+) to CD31 super(-) naive CD4 super(+) T cells. In the longitudinal cohort we then quantified the concentration of HIV-1 DNA in each cell subset and performed single-genome amplification of virus from memory and naive T cells. Results. Patients receiving ART had a higher proportion of CD31 super(+) CD4 super(+) T cells than HIV-1-infected individuals naive to ART and uninfected control subjects (P[inline image]<[inline image].001 and.007, respectively). After 24 months of ART, the proportion of CD31 super(+) naive CD4 super(+) T cells did not change, the concentration of HIV-1 DNA in memory CD4 super(+) T cells significantly decreased over time (P[inline image]<[inline image].001), and there was no change in the concentration of HIV-1 DNA in CD31 super(+) or CD31 super(-) naive CD4 super(+) T cells (P[inline image]=[inline image].751 and.251, respectively). Single-genome amplification showed no evidence of virus compartmentalization in memory and naive T cell subsets before or after ART. Conclusions. After ART, both CD31 super(+) and CD31 super(-) naive CD4 super(+) T cells expand, and both subsets represent a stable, persistent reservoir of HIV-1.
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ISSN:0022-1899
DOI:10.1086/656721