Progressive CD127 down-regulation correlates with increased apoptosis of CD8 T cells during chronic HIV-1 infection

Eur J Immunol. 2009 May;39(5):1425-34. doi: 10.1002/eji.200839059.

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down-regulated CD127 expression, whereas some of the CD127(-) CD8 T cells regained CD127 expression soon after IL-7 was retracted from the incubation medium.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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • Cohort Studies
  • Down-Regulation / immunology
  • Female
  • Flow Cytometry
  • HIV Infections / immunology*
  • HIV-1 / immunology*
  • Humans
  • Immunologic Memory / immunology
  • Immunotherapy / methods
  • In Vitro Techniques
  • Interleukin-7 / pharmacology*
  • Interleukin-7 / therapeutic use
  • Interleukin-7 Receptor alpha Subunit / immunology*
  • Male
  • Middle Aged
  • RNA, Viral / blood
  • Young Adult

Substances

  • IL7 protein, human
  • Interleukin-7
  • Interleukin-7 Receptor alpha Subunit
  • RNA, Viral