Intracellular signalling cascades regulating innate immune responses to Mycobacteria:: branching out from Toll-like receptors

被引:199
作者
Jo, Eun-Kyeong [1 ]
Yang, Chul-Su
Choi, Chul Hee
Harding, Clifford V.
机构
[1] Chungnam Natl Univ, Coll Med, Dept Microbiol, Taejon 301747, South Korea
[2] Chungnam Natl Univ, Coll Med, Med Res Inst, Taejon 301747, South Korea
[3] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
关键词
NECROSIS-FACTOR-ALPHA; BACILLUS-CALMETTE-GUERIN; NF-KAPPA-B; AVIUM SUBSP PARATUBERCULOSIS; ACTIVATED PROTEIN-KINASES; PRO-INFLAMMATORY SIGNALS; P38 MAP KINASE; TUBERCULOSIS INFECTION; GENE-EXPRESSION; DENDRITIC CELLS;
D O I
10.1111/j.1462-5822.2007.00914.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Toll-like receptors (TLRs) recognize Mycobacterium tuberculosis (Mtb) or Mtb components and initiate mononuclear phagocyte responses that influence both innate and adaptive immunity. Recent studies have revealed the intracellular signalling cascades involved in the TLR-initiated immune response to mycobacterial infection. Although both TLR2 and TLR4 have been implicated in host interactions with Mtb, the relationship between specific mycobacterial molecules and various signal transduction pathways is not well understood. This review will discuss recent studies indicating critical roles for mycobacteria and mycobacterial components in regulation of mitogen-activated protein kinases and related signal transduction pathways that govern the outcome of infection and antibacterial defence. To better understand the roles of infection-induced signalling cascades in molecular pathogenesis, future studies are needed to clarify mechanisms that integrate the multiple signalling pathways that are activated by engagement of TLRs by both individual mycobacterial molecules and whole mycobacteria. These efforts will allow for the development of novel diagnostic and therapeutic modalities for tuberculosis that targets the intracellular signalling pathways permitting the replication of this nefarious pathogen.
引用
收藏
页码:1087 / 1098
页数:12
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