AI Article Synopsis

  • Chronic HIV-1 infection leads to a significant reduction in CD127 expression on CD8 T cells, which is associated with increased apoptosis and disease progression in patients.
  • Researchers analyzed blood samples from 51 HIV-1-infected individuals and 16 healthy controls, finding that lower CD127 levels correlate with higher rates of CD8 T-cell death.
  • The study suggests that IL-7 can help reduce T-cell apoptosis, though it initially lowers CD127 expression, indicating that improving IL-7 signaling might be a promising immunotherapy approach for those living with HIV-1.

Article Abstract

Chronic HIV-1 infection can induce a significant decrease in CD127 expression on CD8 T cells, but the underlying mechanisms and immunological consequences are unclear. In this study, we investigated CD127 expression on CD8 T cells from a total of 51 HIV-1-infected subjects and 16 healthy individuals and analyzed the association between CD127 expression and CD8 T-cell apoptosis in these HIV-1-infected subjects. We found that CD127 expression on total CD8 T cells was significantly down-regulated, which was correlated with the increased CD8 T-cell apoptosis and disease progression of chronic HIV-1 infection. The in vitro addition of IL-7 efficiently rescued the spontaneous apoptosis of CD8 T cells from HIV-1-infected individuals. IL-7 stimulation also transiently down-regulated CD127 expression, whereas some of the CD127(-) CD8 T cells regained CD127 expression soon after IL-7 was retracted from the incubation medium. Thus, IL-7 stimulation reduced apoptosis of both CD127(+) and CD127(-)CD8 T cells to some degree. These data indicate that CD127 loss might impair IL-7 signaling and increase CD8 T-cell apoptosis during HIV-1 infection. This study, therefore, will extend the notion that IL-7 could be a good candidate for immunotherapy in HIV-1-infected patients.

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http://dx.doi.org/10.1002/eji.200839059DOI Listing

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