MedicineBiology

S. Sakaguchi, N. Sakaguchi, J. Shimizu, S. Yamazaki, T. Sakihama, M. Itoh, Y. Kuniyasu, T. Nomura, M. Toda, Takeshi Takahashi

2001.8.1IMMUNOLOGICAL REVIEWS

DOI: 10.1034/j.1600-065x.2001.1820102.x

tlooto Summary

There is accumulating evidence that T‐cell‐mediated dominant control of self‐reactive T‐cells contributes to the maintenance of immunologic self‐tolerance and its alteration can cause autoimmune disease.

Abstract

Summary: There is accumulating evidence that T‐cell‐mediated dominant control of self‐reactive T‐cells contributes to the maintenance of immunologic self‐tolerance and its alteration can cause autoimmune disease. Efforts to delineate such a regulatory T‐cell population have revealed that CD25 + cells in the CD4 + population in normal naive animals bear the ability to prevent autoimmune disease in vivo and, upon antigenic stimulation, suppress the activation/proliferation of other T cells in vitro . The CD25 + CD4 + regulatory T cells, which are naturally anergic and suppressive, appear to be produced by the normal thymus as a functionally distinct subpopulation of T cells. They play critical roles not only in preventing autoimmunity but also in controlling tumor immunity and transplantation tolerance.

Citation format

SAKAGUCHI, S., et al. Immunologic tolerance maintained by CD25+ CD4+ regulatory t cells: Their common role in controlling autoimmunity, tumor immunity, and transplantation tolerance. IMMUNOLOGICAL REVIEWS, 2001, 182.