Overexpression of monosialoganglioside GM3 on lymphocyte plasma membrane in patients with HIV infection

J Acquir Immune Defic Syndr Hum Retrovirol. 1996 Jun 1;12(2):112-9. doi: 10.1097/00042560-199606010-00003.

Abstract

This study was undertaken to analyze both the GM3 expression on peripheral blood lymphocytes of HIV-infected patients and the relationship between ganglioside content and anti-GM3 reactivity. GM3 expression was determined as a percentage of lipid-bound sialic acid and by cytofluorimetric analysis in 25 AIDS patients, 20 anti-HIV+ asymptomatic subjects, 25 patients with different viral disease, and 25 healthy donors. GM3 distribution was analyzed by immunofluorescence and immunoelectron microscopy. A follow-up study to detect anti-lymphocytic GM3 antibodies was performed in progressive and nonprogressive anti-HIV+ subjects. Lymphocytes from HIV-infected patients showed a significant increase of plasma membrane GM3 content; no difference was found between CD4+ and CD8+ cells. Immunofluorescence and immunoelectron microscopic analysis showed that GM3 was distributed in large clusters over the cell plasma membrane. The follow-up study revealed that the occurrence of anti-lymphocytic GM3 antibodies was significantly higher in patients with progressive disease, compared with asymptomatic non-progressive subjects. These findings revealed that (1) the increased GM3 content in HIV-infected patients is detected at the plasma membrane level, (2) GM3 overexpression is able to induce an increased reactivity with anti-GM3 antibodies, and (3) the appearance of anti-lymphocytic GM3 antibodies in asymptomatic anti-HIV+ subjects could have prognostic relevance for the risk of developing AIDS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Autoantibodies / blood
  • Cell Membrane / metabolism
  • Flow Cytometry
  • G(M3) Ganglioside / blood*
  • G(M3) Ganglioside / immunology
  • HIV Infections / blood*
  • HIV Infections / immunology
  • Humans
  • Lymphocytes / metabolism*
  • Lymphocytes / ultrastructure
  • Microscopy, Immunoelectron

Substances

  • Antibodies, Monoclonal
  • Autoantibodies
  • G(M3) Ganglioside