Circulating CD20dim T-lymphocytes increase with age: evidence for a memory cytotoxic phenotype

Clin Lab Haematol. 1995 Dec;17(4):323-8.

Abstract

The CD20 antigen has been regarded as a B lineage specific, 35 kDa, non-glycosylated membrane phosphoprotein, which functions as either a Ca2+ ion channel or as a regulatory protein of such a channel. Weak expression of CD20 (CD20dim), however, has recently been reported on a sub-population of T lymphocytes. We present results which confirm the existence of a CD20dim T lymphocyte population and show that such cells have a reduced antibody-binding capacity, when compared to CD20bright B-cells (10337 +/- 642 and 346311 +/- 24264 respectively). In addition, CD20dim cell counts vary with age, with the highest levels occurring in octogenarians: cord blood 0.3 +/- 0.1% (n = 13), 20-60 year-old group 2.1 +/- 1.1% (n = 18) and individuals > or = 61 years of age 6.9 +/- 3.2% (n = 10) (P < 0.001). Further characterization of CD20dim T cells, using three colour flow cytometry, demonstrated a predominantly memory cytotoxic phenotype, in that the cells were CD8+CD28+CD45RO+T-CR alpha beta +CD38-HLA-DR-.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antigen-Antibody Reactions
  • Antigens, CD20 / blood*
  • Fetal Blood / immunology
  • Flow Cytometry
  • Humans
  • Immunologic Memory*
  • Immunophenotyping
  • Infant, Newborn
  • Middle Aged
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes, Cytotoxic*

Substances

  • Antigens, CD20