Cytokines and transcription factors that regulate T helper cell differentiation: New players and new insights

被引:290
作者
Agnello, D
Lankford, CSR
Bream, J
Morinobu, A
Gadina, M
O'Shea, JJ
Frucht, DM
机构
[1] NIAMSD, Mol Immunol & Inflammat Branch, NIH, Bethesda, MD 20802 USA
[2] US FDA, Div Monoclonal Antibodies, Ctr Biol Evaluat & Res, Bethesda, MD 20014 USA
[3] Queens Univ Belfast, Dept Microbiol & Immunol, Belfast, Antrim, North Ireland
关键词
T helper (T-H) cells; differentiation; T(H)1 cells; T(H)2 cells; interferon-gamma; interleukin (IL)-4; IL-12; IL-23; IL-27; Stat1; Stat4; Stat6; GATA-3; c-Maf; NFATs;
D O I
10.1023/A:1023381027062
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 differentiation of naive CD4(+) T cells into subsets of T helper cells is a pivotal process with major implications for host defense and the pathogenesis of immune-mediated diseases. Though the basic paradigm was discovered more than 15 years ago, new discoveries continue to be made that offer fresh insights into the regulation of this process (1). T helper (T-H)1 cells produce interferon (IFN)-gamma, promoting cell-mediated immunity and control of intracellular pathogens. We now know that T(H)1 differentiation is regulated by transcription factors such as T-bet, Stat1, and Stat4, as well as cytokines such as IL-12, IL-23, IL-27, type I IFNs, and IFN-gamma. In contrast, T(H)2 cells produce IL-4, which promotes allergic responses and is important in host defense against helminths. The transcription factors Stat6, GATA-3, c-Maf, NFATs, and the cytokine IL-4 promote T(H)2 differentiation. These key regulators of T-H differentiation are the subject of this review.
引用
收藏
页码:147 / 161
页数:15
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