Pathogen-associated molecular pattern contamination as putative endogenous ligands of Toll-like receptors.

Min-Fu Tsan, Baochong Gao
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引用次数: 105

Abstract

Extensive work in recent years has suggested that a number of endogenous molecules, their derivatives or degradation products may be potent activators of the innate immune system capable of inducing pro-inflammatory cytokine production by the monocyte-macrophage system and the activation and maturation of dendritic cells. The cytokine-like effects of these endogenous molecules are mediated via Toll-like receptor (TLR) signal transduction pathways in a manner similar to pathogen-associated molecular patterns (PAMPs). However, recent evidence suggests that the reported cytokine effects of some of these putative endogenous ligands are in fact due to contaminating PAMPs. The reasons for the failure to recognize PAMP contaminants being responsible for the putative TLR ligands of these endogenous molecules include: (i) failure to use highly purified preparations free of PAMP contamination; (ii) failure to recognize the heat sensitivity of lipopolysaccharide (LPS); and (iii) failure to consider contaminant(s) other than LPS. Strategies are proposed to avoid future designation of PAMP contamination as putative endogenous ligands of TLRs.

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病原体相关的分子模式污染作为假定的内源性toll样受体配体。
近年来的大量研究表明,许多内源性分子及其衍生物或降解产物可能是先天免疫系统的有效激活剂,能够诱导单核-巨噬细胞系统产生促炎细胞因子,并激活和成熟树突状细胞。这些内源性分子的细胞因子样作用是通过toll样受体(TLR)信号转导途径介导的,其方式类似于病原体相关分子模式(PAMPs)。然而,最近的证据表明,报道的一些这些假定的内源性配体的细胞因子作用实际上是由于污染了PAMPs。未能识别PAMP污染物是这些内源性分子的TLR配体的原因包括:(i)未能使用不含PAMP污染的高纯度制剂;(ii)不能识别脂多糖(LPS)的热敏性;(iii)未能考虑LPS以外的污染物。提出了避免未来将PAMP污染指定为TLRs的假定内源性配体的策略。
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