Concerted effect of lymphopenia, viraemia and T-cell activation on Fas expression of peripheral B cells in HIV-1-infected patients

AIDS. 2013 Jan 14;27(2):155-62. doi: 10.1097/QAD.0b013e32835b8c5e.

Abstract

Objective: Decreased memory B-cell maintenance during HIV-1 infection has been associated with the viraemia-induced accumulation of activated memory B cells, sensitive to Fas-mediated apoptosis. We aimed at clarifying whether other B-cell subsets might also be affected by an increased Fas expression in HIV-1-infected patients, and we studied the possible contribution of viraemia, lymphopenia or T-cell activation in Fas upregulation on B cells. We analysed whether Fas upregulation might have collaborative effects with the dysregulation of other B-cell modulatory molecules, leukocyte-associated immunoglobulin-like receptor 1 (LAIR1) and programmed cell death protein 1 (PD-1), on B-cell homeostasis.

Design: Fas, LAIR1 and PD-1 were analysed on B-cell subpopulations in HIV-1-infected patients who were treatment naive, nonlymphopenic; antiretroviral therapy (ART)-treated, nonlymphopenic; or ART-treated, lymphopenic or in noninfected controls.

Methods: Flow cytometry was used to study B-cell subsets and Milliplex for serum cytokines.

Results: Fas expression increased on all B-cell subpopulations of viraemic or lymphopenic individuals. The decreased ratio of resting memory B cells and their increased Fas expression were not normalized by ART. Cytokines associated with T-cell activation might influence Fas expression on the naive and transitional B cells. LAIR1 expression decreased in all HIV-1-infected patients, but only on memory B cells, whereas PD-1 increased on resting memory B cells in viraemic patients.

Conclusion: Fas is regulated by the concerted action of viraemia, lymphopenia and T-cell activation during HIV-1 infection, and Fas expression is altered on all peripheral B-cell subsets. Resting memory B-cell homeostasis shows the highest sensitivity to HIV-1-induced perturbations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis
  • B-Lymphocytes / immunology
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes / immunology*
  • Female
  • Flow Cytometry
  • HIV Infections / immunology*
  • HIV-1 / physiology
  • Humans
  • Immunologic Memory / immunology
  • Lymphocyte Activation*
  • Lymphopenia / immunology*
  • Male
  • Middle Aged
  • Programmed Cell Death 1 Receptor / metabolism
  • Receptors, Immunologic / metabolism
  • Viremia / immunology*
  • fas Receptor / metabolism*

Substances

  • Programmed Cell Death 1 Receptor
  • Receptors, Immunologic
  • fas Receptor
  • leukocyte-associated immunoglobulin-like receptor 1