Murillo Laura S, Morré Servaas A, Peña A Salvador
Laboratory of Immunogenetics and Department of Gastroenterology, VU University Medical Centre, Amsterdam, The Netherlands.
Drugs Today (Barc). 2003 Jun;39(6):415-38.
The magnitude of the response to a specific immunogen such as an infectious agent is the result of a complex interaction between genetic and environmental factors. For example, in intestinal inflammation, the inflammatory response appears to be regulated by the indigenous microflora of the gut, by receptors in epithelial cells and antigen-presenting cells in the intestinal mucosa, and by immunologic factors. Recent evidence suggests that genetic variants of human immunomodulating genes influence the susceptibility to and severity of infectious diseases and the subsequent clinical outcome of disease. This review will focus on recently identified pattern recognition receptors which are located on innate immune and epithelial cells, and recognize pathogen-associated molecular patterns. The binding of specific pathogen-associated molecular patterns to these receptors results in the activation of a signal transduction pathway through nuclear factor (NF)-kappaB which leads to either enhanced or inhibited immune responses that modify the production of inflammatory effectors, such as cytokines. This article reports on the identification and functional characterization including the discovery of mutants which completely abolish NF-kappaB signal transduction of pattern recognition receptors, such as the extracellular Toll-like receptors and the intracellular nucleotide oligomerization domain/caspase recruitment domain (NOD/CARD) receptors, as well as their role in clinical disease. Knowledge of pattern recognition receptors such as Toll-like receptors and NOD/CARD intracytoplasmic proteins, including their functions and their downstream signaling pathways, may provide a new molecular basis for preventing or blocking inflammation associated with pathogenic microorganisms. This could direct a new focus for better and more specific therapeutic treatments based on immuno-intervention that can promise a better quality of life for those suffering from chronic disturbances of the immune response.
对特定免疫原(如传染原)的反应强度是遗传因素和环境因素之间复杂相互作用的结果。例如,在肠道炎症中,炎症反应似乎受肠道固有微生物群、上皮细胞和肠黏膜中抗原呈递细胞的受体以及免疫因素的调节。最近的证据表明,人类免疫调节基因的遗传变异会影响传染病的易感性和严重程度以及疾病的后续临床结果。本综述将聚焦于最近发现的模式识别受体,这些受体位于天然免疫细胞和上皮细胞上,可识别病原体相关分子模式。特定病原体相关分子模式与这些受体的结合会通过核因子(NF)-κB激活信号转导途径,进而导致免疫反应增强或抑制,从而改变炎症效应分子(如细胞因子)的产生。本文报道了模式识别受体的鉴定和功能表征,包括发现完全消除NF-κB信号转导的突变体,如细胞外Toll样受体和细胞内核苷酸寡聚化结构域/半胱天冬酶招募结构域(NOD/CARD)受体,以及它们在临床疾病中的作用。了解Toll样受体和NOD/CARD胞质内蛋白等模式识别受体,包括它们的功能及其下游信号通路,可能为预防或阻断与致病微生物相关的炎症提供新的分子基础。这可能会为基于免疫干预的更好、更特异性的治疗方法指引新的方向,有望为那些患有免疫反应慢性紊乱的患者带来更高的生活质量。