Massive activation of immune cells with an intact T cell repertoire in acute human immunodeficiency virus syndrome

J Infect Dis. 1995 Jul;172(1):105-12. doi: 10.1093/infdis/172.1.105.

Abstract

In 8 patients with symptomatic, acute primary infection with human immunodeficiency virus (HIV), a dramatic and persistent decrease in CD4+ lymphocytes was seen, accompanied by a marked increase in activated/memory CD8+ T cells (CD38+, CD45R0+, HLA-DR+, with high amounts of cell adhesion molecules), which represented most circulating lymphocytes, but no gross alterations in V beta T cell repertoire. Extremely high plasma levels of proinflammatory cytokines were observed. Three patients were followed for 2-3 years: The number of CD4+ cells, extremely low at first, increased significantly in a few months but decreased rapidly after a short stable period. Cytotoxic T lymphocytes bearing markers of immunologic activation/memory could play an important role in the earliest phases of the disease. It remains to be established how such a dramatic onset could determine the rapid progression of the infection that seems characteristic of patients with acute HIV syndrome.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / immunology*
  • Adult
  • Antigens, CD / blood
  • Biomarkers
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Female
  • Fluorescent Antibody Technique
  • HIV Antibodies / blood
  • HIV Core Protein p24 / blood
  • HIV Seropositivity / immunology
  • HIV-1*
  • HLA-DR Antigens / blood
  • Humans
  • Immunophenotyping
  • Lymphocyte Activation*
  • Male
  • Receptors, Antigen, T-Cell, alpha-beta / analysis
  • Reference Values
  • T-Lymphocytes / immunology*

Substances

  • Antigens, CD
  • Biomarkers
  • HIV Antibodies
  • HIV Core Protein p24
  • HLA-DR Antigens
  • Receptors, Antigen, T-Cell, alpha-beta