articleJournal of Clinical InvestigationNov 1, 2003BRONZE OA

Induction of FoxP3 and acquisition of T regulatory activity by stimulated human CD4+CD25– T cells

Pacific Northwest Diabetes Research Institute · Virginia Mason Medical Center

PubMed
Indexed incrossrefdoajpubmed

Abstract

CD4+CD25+ regulatory T (TR) cells have been described in both humans and mice. In mice, TR are thymically derived, and lack of TR leads to organ-specific autoimmunity. Recently, the forkhead/winged helix transcription factor, FoxP3, has been shown to be important for the function of TR cells in mice. In this study, human TR cells were examined and, in results similar to those of studies done in mice, expression of FoxP3 was found exclusively in CD4+CD25+ T cells and correlated with the suppressive activity of these cells. In contrast to the mouse studies, activation of human CD4+CD25- T cells led to expression of FoxP3. Expression of FoxP3 in activated human CD4+CD25+ cells also correlated with suppression of…

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Authors

7

Topics & keywords

Keywords
  • IL-2 receptor
  • FOXP3
  • Interleukin 21
  • Biology
  • Cell biology
  • Immune system
  • T cell
  • Immunology
UN Sustainable Development Goals
  • Good health and well-being
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