首页> 美国卫生研究院文献>Reumatologia >U1-RNP and Toll-like receptors in the pathogenesis of mixed connective tissue diseasePart II. Endosomal TLRs and their biological significance in the pathogenesis of mixed connective tissue disease
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U1-RNP and Toll-like receptors in the pathogenesis of mixed connective tissue diseasePart II. Endosomal TLRs and their biological significance in the pathogenesis of mixed connective tissue disease

机译:U1-RNP和Toll样受体在混合性结缔组织病发病机制中的作用第二部分。内体TLR及其在混合性结缔组织病发病机理中的生物学意义

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摘要

Mixed connective tissue disease (MCTD) is a chronic autoimmune immunopathological disease of unknown etiology, which is characterized by the presence of various clinical symptoms and the presence of autoantibodies against U1-RNP particles. The U1-RNP component engages immune cells and their receptors in a complex network of interactions that ultimately lead to autoimmunity, inflammation, and tissue injury. The anti-U1-RNP autoantibodies form an immune complex with self-RNA, present in MCTD serum, which can act as endosomal Toll-like receptor (TLR) ligands. Inhibition of TLRs by nucleic acids is a promising area of research for the development of novel therapeutic strategies against pathogenic infection, tumorigenesis and autoimmunity. In this review we summarize current knowledge of endogenous TLRs and discuss their biological significance in the pathogenesis of MCTD. In part I we described the structure, biological function and significance of the U1-RNP complex in MCTD.
机译:混合性结缔组织病(MCTD)是一种病因不明的慢性自身免疫性免疫病理疾病,其特征是存在多种临床症状和针对U1-RNP颗粒的自身抗体。 U1-RNP成分在复杂的相互作用网络中与免疫细胞及其受体结合,最终导致自身免疫,炎症和组织损伤。抗U1-RNP自身抗体与存在于MCTD血清中的自身RNA形成免疫复合物,可以充当内体Toll样受体(TLR)配体。核酸抑制TLRs是开发针对病原体感染,肿瘤发生和自身免疫的新型治疗策略的有前途的研究领域。在这篇综述中,我们总结了目前内源性TLR的知识,并讨论了它们在MCTD发病机理中的生物学意义。在第一部分中,我们描述了MCTD中U1-RNP复合物的结构,生物学功能和意义。

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