Stability of the Regulatory T Cell Lineage in Vivo

Author:

Rubtsov Yuri P.1,Niec Rachel E.1,Josefowicz Steven1,Li Li2,Darce Jaime2,Mathis Diane2,Benoist Christophe2,Rudensky Alexander Y.1

Affiliation:

1. Howard Hughes Medical Institute and Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.

2. Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.

Abstract

Self-Renewing T Cells The homeostasis of cell populations within an organism can be achieved through a variety of mechanisms, including the differentiation of precursor populations, self-renewal of terminally differentiated cells, or by programming cells to be extremely long-lived. Regulatory T cells that express the transcription factor Foxp3 are critical for maintaining immune tolerance by preventing excessive inflammation and autoimmunity. Rubtsov et al. (p. 1667 ) now use genetic fate mapping and cell transfer studies in vivo to demonstrate that Foxp3-expressing cells are remarkably stable under both basal and inflammatory conditions. Thus, regulatory T cells appear to be maintained through self-renewal and should maintain their identity if used in adoptive cell therapies for treatment of autoimmunity or other inflammatory disorders.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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