Functional assay for human CD4+CD25+ Treg cells reveals an age-dependent loss of suppressive activity

Laura Tsaknaridis, Leslie Spencer, Nicole Culbertson, Kevin Hicks, Dorian LaTocha, Yuan K. Chou, Ruth H. Whitham, Antony Bakke, Richard E. Jones, Halina Offner, Dennis N. Bourdette, Arthur A. Vandenbark

Research output: Contribution to journalArticle

145 Scopus citations

Abstract

CD4+CD25+ regulatory T cells (Treg cells) prevent T cell-mediated autoimmune diseases in rodents. To develop a functional Treg assay for human blood cells, we used FACS- or bead-sorted CD4 +CD25+ T cells from healthy donors to inhibit anti-CD3/CD28 activation of CD4+CD25- indicator T cells. The data clearly demonstrated classical Treg suppression of CD4 +CD25- indicator cells by both CD4+CD25 +high and CD4+CD25+low T cells obtained by FACS or magnetic bead sorting. Suppressive activity was found in either CD45RO- (naive) or CD45RO+ (memory) subpopulations, was independent of the TCR signal strength, required cell-cell contact, and was reversible by interleukin-2 (IL-2). Of general interest is that a wider sampling of 27 healthy donors revealed an age- but not gender-dependent loss of suppressive activity in the CD4+CD25+ population. The presence or absence of suppressive activity in CD4+CD25+ T cells from a given donor could be demonstrated consistently over time, and lack of suppression was not due to method of sorting, strength of signal, or sensitivity of indicator cells. Phenotypic markers did not differ on CD4 +CD25+ T cells tested ex vivo from suppressive vs. nonsuppressive donors, although, upon activation in vitro, suppressive CD4 +CD25+ T cells had significantly higher expression of both CTLA-4 and GITR than CD4+CD25- T cells from the same donors. Moreover, antibody neutralization of CTLA-4, GITR, IL-10, or IL-17 completely reversed Treg-induced suppression. Our results are highly consistent with those reported for murine Treg cells and are the first to demonstrate that suppressive activity of human CD4+CD25+ T cells declines with age.

Original languageEnglish (US)
Pages (from-to)296-308
Number of pages13
JournalJournal of Neuroscience Research
Volume74
Issue number2
DOIs
StatePublished - Oct 15 2003

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Keywords

  • Age dependence
  • Human CD4CD25 T cells
  • Regulatory T cells

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience

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