Toll-like receptor regulation of effector T lymphocyte function

被引:118
作者
Reynolds, Joseph M. [1 ,2 ,3 ]
Dong, Chen [1 ,2 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Ctr Inflammat & Canc, Houston, TX 77030 USA
[3] Rosalind Franklin Univ Med & Sci, Dept Microbiol & Immunol, N Chicago, IL 60064 USA
关键词
Toll-like receptors; T lymphocytes; gamma/delta T cells; NKT cells; ESCHERICHIA-COLI INFECTION; IFN-GAMMA PRODUCTION; B-CELL RESPONSES; NKT CELLS; SIGNALING PATHWAY; CPG-OLIGODEOXYNUCLEOTIDES; TLR2; ENGAGEMENT; CUTTING EDGE; IMMUNE REGULATION; IL-4; PRODUCTION;
D O I
10.1016/j.it.2013.06.003
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 landmark discovery of pattern-recognition receptors, including Toll-like receptors (TLRs), furthered our understanding on how the host rapidly responds to invading pathogens. For over a decade now, extensive research has demonstrated the crucial role of multiple TLRs in the detection of a broad range of molecules expressed by microbial pathogens as well as host-derived danger signals. TLR activation is the hallmark of the innate immune response. Recent evidence, however, demonstrates that cells of the adaptive immune response use these innate signaling pathways as well. This review discusses recent findings regarding TLR functionality in T lymphocytes with a specific emphasis on the promotion of T helper cell-dependent inflammation through direct TLR signaling.
引用
收藏
页码:511 / 519
页数:9
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