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Cycling of Gut Mucosal CD4+ T Cells Decreases after Prolonged Anti-Retroviral Therapy and is Associated with Plasma LPS Levels

The gut mucosa is an important site of HIV immunopathogenesis, with severe depletion of CD4+ T cells occurring during acute infection. The effect of prolonged anti-retroviral therapy (ART) on cycling and restoration of T lymphocytes in the gut remains unclear. Colon and terminal ileal biopsies and p...

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Detalles Bibliográficos
Autores principales: Ciccone, Emily J., Read, Sarah W., Mannon, Peter J., Yao, Michael D., Hodge, Jessica N., Dewar, Robin, Chairez, Cheryl L., Proschan, Michael A., Kovacs, Joseph A., Sereti, Irini
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2830855/
https://www.ncbi.nlm.nih.gov/pubmed/19956090
http://dx.doi.org/10.1038/mi.2009.129
Descripción
Sumario:The gut mucosa is an important site of HIV immunopathogenesis, with severe depletion of CD4+ T cells occurring during acute infection. The effect of prolonged anti-retroviral therapy (ART) on cycling and restoration of T lymphocytes in the gut remains unclear. Colon and terminal ileal biopsies and peripheral blood samples were collected from viremic, untreated, HIV-infected participants, patients treated with prolonged ART (>5 years), and uninfected controls and analyzed by flow cytometry. In the gut, the proportion of cycling T cells decreased and the number of CD4+ T cells normalized in treated patients in parallel with β7 expression on CD4+ T cells in blood. Cycling of gut T cells in viremic patients was associated with increased plasma LPS levels, but not colonic HIV-RNA. These data suggest that gut T cell activation and microbial translocation may be interconnected while prolonged ART may decrease activation and restore gut CD4+ T cells.