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Regulation of T:B cell interactions by the Inducible Costimulator molecule:: Does ICOS "induce" disease?
被引:25
|作者:
Shilling, Rebecca A.
Bandukwala, Hozefa S.
Sperling, Anne I.
机构:
[1] Univ Chicago, Dept Med, Sect Pulm & Crit Care, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
关键词:
ICOS;
T cells;
B cells;
follicular T helper cells;
autoimmunity;
allergy;
asthma;
polymorphisms;
humoral immunity;
D O I:
10.1016/j.clim.2006.04.574
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The Inducible Costimulator molecule (ICOS), a member of the CD28 family of costimulatory molecules, was identified in 1999 as a molecule expressed primarily on activated human T cells. Induced upon activation, ICOS appears to be an ideal target for modifying T-cell-mediated immune responses. ICOS was also found to be highly expressed on germinal center T cells, suggesting that ICOS was involved in T-B cell interactions. While ICOS has subsequently been shown to be important for both Th1 and Th2 cell activation and effector function, a central role for ICOS in the generation and maintenance of humoral immunity is emerging. In this review, we summarize the evidence that the level of ICOS expression regulates T-cell-dependent B cell responses and propose a model for the rote of ICOS in diseases characterized by dysregulated humoral immunity. (c) 2006 Elsevier Inc. All rights reserved.
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页码:13 / 18
页数:6
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