TLR signaling pathways: Opportunities for activation and blockade in pursuit of therapy

被引:57
作者
Hoebe, K.
Jiang, Z.
Georgel, P.
Tabeta, K.
Janssen, E.
Du, X.
Beutler, B.
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[2] Niigata Univ, Grad Sch Med & Dent Sci, Dept Oral Biol Sci, Div Periodontol, Niigata 9518514, Japan
[3] La Jolla Inst Allergy & Immunol, Dept Dev Immunol, San Diego, CA USA
关键词
D O I
10.2174/138161206778743466
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The identification of the TLRs as key sensors of microbial infection has presented a series of new targets for drug development. The TLRs are linked to the most powerful inflammatory pathways in mammals. The question arises from the start: do we wish to stimulate TLR signaling in order to eradicate specific infections and/or neoplastic diseases? Or do we wish to block TLR signaling to treat inflammatory diseases? If we accept that it would be useful to modulate TLR signaling, the next step is to identify the correct molecular target(s) for the task. Perhaps it might even be possible to exercise selectivity, modulating some aspects of TLR signaling and not others. Classical and reverse genetic analyses offer insight into the possibilities that exist, and point to specific checkpoints within signaling pathways at which modulation might normally be imposed.
引用
收藏
页码:4123 / 4134
页数:12
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