Potential deleterious effect of anti-viral cytotoxic lymphocyte through the CD95 (FAS/APO-1)-mediated pathway during chronic HIV infection

Immunol Lett. 1997 Jun 1;57(1-3):53-8. doi: 10.1016/s0165-2478(97)00070-9.

Abstract

The potential deleterious effect through a CD95-based pathway of anti-viral cytotoxic lymphocyte (CTL) during HIV-infection was studied. The present paper reports that a Nef specific CTL line derived from an HIV-infected person is able to kill not only Nef-expressing target cells but also CD95+ compliant Jurkat cells. The two mechanisms of cytotoxicity, i.e. perforin-vs-CD95-dependent were differentiated according to their respective Ca(2+)-dependence. The existence of the dual killing machinery in the anti-HIV CTL line was correlated with the coexpression in these cells of perforin and CD95-L molecules. A model of AIDS pathogenesis involving the deleterious effect through the CD95 pathway of the viral specific CTL response is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigen-Presenting Cells / immunology
  • Calcium / immunology
  • Cell Line
  • Cell Line, Transformed
  • Chronic Disease
  • Cytotoxicity Tests, Immunologic
  • Fas Ligand Protein
  • Gene Products, nef / immunology*
  • HIV Infections / immunology*
  • Humans
  • Jurkat Cells
  • Membrane Glycoproteins / biosynthesis
  • Perforin
  • Pore Forming Cytotoxic Proteins
  • T-Lymphocytes, Cytotoxic / cytology
  • T-Lymphocytes, Cytotoxic / immunology*
  • fas Receptor / immunology*
  • nef Gene Products, Human Immunodeficiency Virus

Substances

  • FASLG protein, human
  • Fas Ligand Protein
  • Gene Products, nef
  • Membrane Glycoproteins
  • Pore Forming Cytotoxic Proteins
  • fas Receptor
  • nef Gene Products, Human Immunodeficiency Virus
  • Perforin
  • Calcium