Expression of CD69 after in vitro stimulation: a rapid method for quantitating impaired lymphocyte responses in HIV-infected individuals

J Acquir Immune Defic Syndr Hum Retrovirol. 1996 Jan 1;11(1):95-104. doi: 10.1097/00042560-199601010-00013.

Abstract

A flow cytometric assay based on expression of the activation antigen CD69 was developed to analyze immunological responses of T cells from human immunodeficiency virus (HIV)-infected (HIV+) or HIV-seronegative (HIV-) donors after in vitro simulation by antigens and polyclonal activators. The levels of CD69 on freshly-isolated or unstimulated, cultured CD3+, CD4+, or CD8+ peripheral blood lymphocyte (PBL) subsets were low and did not differ greatly between HIV+ and HIV- donors. The frequencies of CD3+, CD4+, and CD8+ lymphocytes from HIV+ donors that expressed CD69 after culture with antigenic or mitogenic stimuli were significantly lower than in HIV- donors. Comparison of CD69 expression with [3H]thymidine incorporation revealed that both assays could detect lymphocyte responses to antigenic or mitogenic stimuli. The CD3+ PBL from HIV+ or HIV- donors did not show increased CD69 expression after culture with soluble or cross-linked recombinant envelope glycoprotein, gp120. The gp120, however, significantly inhibited CD69 expression in phytohemagglutinin-stimulated T cells in vitro and may also affect T-cell activation in vivo. These studies demonstrate the usefulness of this CD69 expression assay for the rapid assessment of defects in immune responses of phenotypically defined lymphocyte subsets in HIV+ patients and for testing the effects of agents that modulate immune activation.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, CD / biosynthesis*
  • Antigens, Differentiation, T-Lymphocyte / biosynthesis*
  • CD3 Complex / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • Cells, Cultured
  • DNA Replication
  • Flow Cytometry
  • HIV Envelope Protein gp120 / pharmacology
  • HIV Infections / immunology*
  • HIV Seropositivity / immunology
  • Humans
  • Immunophenotyping
  • Lectins, C-Type
  • Lymphocyte Activation* / drug effects
  • Male
  • Mitogens / pharmacology
  • Prospective Studies
  • Recombinant Proteins
  • Thymidine / metabolism

Substances

  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CD3 Complex
  • CD69 antigen
  • HIV Envelope Protein gp120
  • Lectins, C-Type
  • Mitogens
  • Recombinant Proteins
  • Thymidine