Immunologic tolerance maintained by CD25<sup>+</sup> CD4<sup>+</sup> regulatory T cells: their common role in controlling autoimmunity, tumor immunity, and transplantation tolerance
抄録
<jats:p><jats:bold>Summary:</jats:bold> 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<jats:sup>+</jats:sup> cells in the CD4<jats:sup>+</jats:sup> population in normal naive animals bear the ability to prevent autoimmune disease <jats:italic>in vivo</jats:italic> and, upon antigenic stimulation, suppress the activation/proliferation of other T cells <jats:italic>in vitro</jats:italic>. The CD25<jats:sup>+</jats:sup> CD4<jats:sup>+</jats:sup> 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.</jats:p>
収録刊行物
-
- Immunological Reviews
-
Immunological Reviews 182 (1), 18-32, 2001-08
Wiley
- Tweet
詳細情報 詳細情報について
-
- CRID
- 1360855571166271744
-
- NII論文ID
- 30013451208
-
- ISSN
- 1600065X
- 01052896
-
- データソース種別
-
- Crossref
- CiNii Articles