High cell surface expression of CD4 allows distinction of CD4+CD25+ antigen-specific effector T cells from CD4+CD25+ regulatoiy T cells in murine experimental autoimmune encephalomyelitis

被引:10
作者
Li, Jinzhu [1 ]
Ridgway, William [3 ]
Fathman, C. Garrison [2 ]
Tse, Harley Y. [1 ]
Shaw, Michael K. [1 ]
机构
[1] Wayne State Univ, Sch Med, Dept Immunol & Microbiol, Detroit, MI 48201 USA
[2] Stanford Univ, Sch Med, Div Immunol & Rheumatol, Dept Med, Stanford, CA 94040 USA
[3] Univ Pittsburgh, Sch Med, Dept Med, Div Rheumatol & Immunol, Pittsburgh, PA 15261 USA
关键词
experimental autoimmune encephalomyelitis; CD4; CD25; T cells; cellular proliferation; FACS; treg;
D O I
10.1016/j.jneuroim.2007.09.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Analysis of T regulatory cells (Treg) and T effector cells (Teff) in experimental autoimmune encephalomyelitis is complicated by the fact that both cell types express CD4 and CD25. We demonstrate that encephalitogenic T cells, following antigen recognition, up-regulate cell surface expression of CD4. The CD4(high) sub-population contains all of the antigen response as shown by proliferation and cytokine secretion, and only these cells are capable of transferring EAE to naive animals. On the other hand, a FACS separable CD25(+) sub-population of cells displayed consistent levels of CD4 prior to and after antigen stimulation. These cells displayed characteristics of Treg, such as expressing high levels of the Foxp3 gene and the ability to suppress mitogenic T cell responses. (c) 2007 Elsevier B.V All rights reserved.
引用
收藏
页码:57 / 67
页数:11
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