Perturbations in B cell responsiveness to CD4+ T cell help in HIV-infected individuals

Proc Natl Acad Sci U S A. 2003 May 13;100(10):6057-62. doi: 10.1073/pnas.0730819100. Epub 2003 May 1.

Abstract

HIV infection induces a wide array of B cell dysfunctions. We have characterized the effect of plasma viremia on the responsiveness of B cells to CD4(+) T cell help in HIV-infected patients. In HIV-negative donors, B cell proliferation correlated with CD154 expression on activated CD4(+) T cells and with the availability of IL-2, whereas in HIV-infected viremic patients, reduced B cell proliferation was observed despite normal CD154 expression on activated CD4(+) T cells. Reduced triggering of B cells by activated CD4(+) T cells was clearly observed in HIV-infected viremic patients compared with aviremic patients with comparable CD4(+) T cell counts, and a dramatic improvement in B cell function was observed in patients whose plasma viremia was controlled by effective antiretroviral therapy. The degree of B cell dysfunction in viremic patients correlated strongly with the inability of B cells to express CD25 in response to activated CD4(+) T cells, resulting in an inability to mount a normal proliferative response to IL-2. Similar defects in responsiveness to IL-2 were observed in the B cells of HIV-infected viremic patients in the context of B cell receptor stimulation. These data provide new insight into the mechanisms associated with ineffective humoral responses in HIV disease.

Publication types

  • Comparative Study

MeSH terms

  • Antigens, CD / blood
  • B-Lymphocytes / immunology*
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes / immunology*
  • CD40 Ligand / blood*
  • Cell Culture Techniques
  • Cross-Sectional Studies
  • Flow Cytometry
  • HIV Infections / blood
  • HIV Infections / immunology*
  • Humans
  • Interleukin-2 / blood
  • Interleukin-2 / metabolism
  • Lymphocyte Activation*
  • Reference Values
  • Viral Load
  • Viremia / blood
  • Viremia / immunology

Substances

  • Antigens, CD
  • Interleukin-2
  • CD40 Ligand