Resting regulatory CD4 T cells: a site of HIV persistence in patients on long-term effective antiretroviral therapy |
| |
Authors: | Tran Tu-Anh de Goër de Herve Marie-Ghislaine Hendel-Chavez Houria Dembele Bamory Le Névot Emilie Abbed Karim Pallier Coralie Goujard Cécile Gasnault Jacques Delfraissy Jean-François Balazuc Anne-Marie Taoufik Yassine |
| |
Institution: | INSERM U802, Université Paris 11, Le Kremlin Bicêtre, France. |
| |
Abstract: | BackgroundIn HIV-infected patients on long-term HAART, virus persistence in resting long-lived CD4 T cells is a major barrier to curing the infection. Cell quiescence, by favouring HIV latency, reduces the risk of recognition and cell destruction by cytotoxic lymphocytes. Several cell-activation-based approaches have been proposed to disrupt cell quiescence and then virus latency, but these approaches have not eradicated the virus. CD4+CD25+ regulatory T cells (Tregs) are a CD4+ T-cell subset with particular activation properties. We investigated the role of these cells in virus persistence in patients on long-term HAART.Methodology/Principal FindingsWe found evidence of infection of resting Tregs (HLADR?CD69?CD25hiFoxP3+CD4+ T cells) purified from patients on prolonged HAART. HIV DNA harbouring cells appear more abundant in the Treg subset than in non-Tregs. The half-life of the Treg reservoir was estimated at 20 months. Since Tregs from patients on prolonged HAART showed hyporesponsiveness to cell activation and inhibition of HIV-specific cytotoxic T lymphocyte-related functions upon activation, therapeutics targeting cell quiescence to induce virus expression may not be appropriate for purging the Treg reservoir.ConclusionsOur results identify Tregs as a particular compartment within the latent reservoir that may require a specific approach for its purging. |
| |
Keywords: | |
本文献已被 PubMed 等数据库收录! |
|