Decreased survival of B cells of HIV-viremic patients mediated by altered expression of receptors of the TNF superfamily

J Exp Med. 2004 Sep 6;200(5):587-99. doi: 10.1084/jem.20032236.

Abstract

Human immunodeficiency virus (HIV) infection leads to numerous perturbations of B cells through mechanisms that remain elusive. We performed DNA microarray, phenotypic, and functional analyses in an effort to elucidate mechanisms of B cell perturbation associated with ongoing HIV replication. 42 genes were up-regulated in B cells of HIV-viremic patients when compared with HIV-aviremic and HIV-negative patients, the majority of which were interferon (IFN)-stimulated or associated with terminal differentiation. Flow cytometry confirmed these increases and indicated that CD21(low) B cells, enhanced in HIV-viremic patients, were largely responsible for the changes. Increased expression of the tumor necrosis factor (TNF) superfamily (TNFSF) receptor CD95 correlated with increased susceptibility to CD95-mediated apoptosis of CD21(low) B cells, which, in turn, correlated with HIV plasma viremia. Increased expression of BCMA, a weak TNFSF receptor for B lymphocyte stimulator (BLyS), on CD21(low) B cells was associated with a concomitant reduction in the expression of the more potent BLyS receptor, BAFF-R, that resulted in reduced BLyS binding and BLyS-mediated survival. These findings demonstrate that altered expression of genes associated with IFN stimulation and terminal differentiation in B cells of HIV-viremic patients lead to an increased propensity to cell death, which may have substantial deleterious effects on B cell responsiveness to antigenic stimulation.

MeSH terms

  • ADP-ribosyl Cyclase / biosynthesis
  • ADP-ribosyl Cyclase 1
  • Antigens, CD / biosynthesis
  • Apoptosis
  • B-Lymphocytes / cytology*
  • B-Lymphocytes / pathology
  • B-Lymphocytes / virology*
  • Cell Differentiation
  • Cell Membrane / metabolism
  • Cell Separation
  • Flow Cytometry
  • HIV Infections / blood*
  • HIV Seropositivity*
  • Humans
  • Interferons / metabolism
  • Membrane Glycoproteins
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Receptors, Complement 3d / biosynthesis
  • Up-Regulation
  • fas Receptor / biosynthesis

Substances

  • Antigens, CD
  • Membrane Glycoproteins
  • Receptors, Complement 3d
  • fas Receptor
  • Interferons
  • ADP-ribosyl Cyclase
  • CD38 protein, human
  • ADP-ribosyl Cyclase 1