Sirard Jean-Claude, Vignal Cécile, Dessein Rodrigue, Chamaillard Mathias
NSERM, U801, Institut Pasteurde Lille, Université Lille 2, Lille, France.
PLoS Pathog. 2007 Dec 28;3(12):e152. doi: 10.1371/journal.ppat.0030152.
In mammals, tissue-specific sets of pattern-recognition molecules, including Nod-like receptors (NLR), enable concomitant and sequential detection of microbial-associated molecular patterns from both the extracellular and intracellular microenvironment. Repressing and de-repressing the cytosolic surveillance machinery contributes to vital immune homeostasis and protective responses within specific tissues. Conversely, defective biology of NLR drives the development of recurrent infectious, autoimmune and/or inflammatory diseases by failing to mount barrier functions against pathogens, to tolerate commensals, and/or to instruct the adaptive immune response against microbes. Better decoding microbial strategies that are evolved to circumvent NLR sensing will provide clues for the development of rational therapies aimed at curing and/or preventing common and emerging immunopathologies.
在哺乳动物中,包括Nod样受体(NLR)在内的组织特异性模式识别分子组,能够同时并相继地检测来自细胞外和细胞内微环境的微生物相关分子模式。抑制和解除对胞质监测机制的抑制有助于特定组织内至关重要的免疫稳态和保护性反应。相反,NLR的生物学功能缺陷会导致复发性感染性、自身免疫性和/或炎性疾病的发生,因为它无法对病原体发挥屏障功能、无法耐受共生菌和/或无法指导针对微生物的适应性免疫反应。更好地解读为规避NLR感知而进化出的微生物策略,将为开发旨在治愈和/或预防常见及新出现的免疫病理学疾病的合理疗法提供线索。