Memory T cells constitute a subset of the human CD8+CD45RA+ pool with distinct phenotypic and migratory characteristics

J Immunol. 2001 Jul 1;167(1):212-20. doi: 10.4049/jimmunol.167.1.212.

Abstract

Using HLA class I-viral epitope tetramers to monitor herpes virus-specific CD8(+) T cell responses in humans, we have shown that a significant fraction of responding cells revert from a CD45RO(+) to a CD45RA(+) state after priming. All tetramer-binding CD45RA(+) cells, regardless of epitope specificity, expressed a phenotype LFA-1(high)CCR7(low) that was stable for at least 10 years in infectious mononucleosis patients and indefinitely in asymptomatic carriers. CD8(+)CD45RA(+)LFA-1(high) cells were not present in cord blood but in adults account for up to 50% of CD8(+)CD45RA(+) cells. These CD45RA(+)LFA-1(high) cells have significantly shorter telomeres than CD45RA(+)LFA-1(low) cells, suggesting that the latter represent a naive population, while the former are memory cells. CD45RA(+) memory cells are a stable population of noncycling cells, but on stimulation they are potent producers of IFN-gamma, while naive CD8(+) cells produce only IL-2. The chemokine receptor profile and migratory potential of CD45RA(+) memory cells is very similar to CD45RO(+) cells but different to naive CD8 cells. In accord with this, CD45RA(+) memory cells were significantly underrepresented in lymph nodes, but account for virtually all CD8(+)CD45RA(+) T cells in peripheral tissues of the same individuals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / immunology
  • CD8-Positive T-Lymphocytes / cytology*
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Cell Division / immunology
  • Cell Movement / immunology*
  • Chemotaxis, Leukocyte / immunology
  • Epitopes, T-Lymphocyte / metabolism
  • HLA-A2 Antigen / metabolism
  • HLA-B8 Antigen / metabolism
  • Humans
  • Immunologic Memory*
  • Immunophenotyping*
  • Interphase / immunology
  • Leukocyte Common Antigens / biosynthesis*
  • Lymphocyte Function-Associated Antigen-1 / biosynthesis
  • Organ Specificity / immunology
  • Peptide Fragments / immunology
  • Peptide Fragments / metabolism
  • Receptors, CCR5 / biosynthesis
  • Receptors, CCR7
  • Receptors, Chemokine / biosynthesis
  • T-Lymphocyte Subsets / cytology*
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism

Substances

  • CCR7 protein, human
  • Epitopes, T-Lymphocyte
  • HLA-A2 Antigen
  • HLA-B8 Antigen
  • Lymphocyte Function-Associated Antigen-1
  • Peptide Fragments
  • Receptors, CCR5
  • Receptors, CCR7
  • Receptors, Chemokine
  • Leukocyte Common Antigens