Department of Biological Sciences, Virginia Tech, Blacksburg, VA, United States.
Department of Pediatrics, School of Medicine, Indiana University Bloomington, Indianapolis, IN, United States.
Front Immunol. 2018 Jul 30;9:1507. doi: 10.3389/fimmu.2018.01507. eCollection 2018.
Allergens are molecules that elicit a hypersensitive inflammatory response in sensitized individuals and are derived from a variety of sources. Alt a 1 is the most clinically important secreted allergen of the ubiquitous fungus, . It has been shown to be a major allergen causing IgE-mediated allergic response in the vast majority of -sensitized individuals. However, no studies have been conducted in regards to the innate immune eliciting activities of this clinically relevant protein. In this study, recombinant Alt a 1 was produced, purified, labeled, and incubated with BEAS-2B, NHBE, and DHBE human lung epithelial cells. Alt a 1 elicited strong induction of IL-8, MCP-1, and Gro-a/b/g. Using gene-specific siRNAs, blocking antibodies, and chemical inhibitors such as LPS-RS, it was determined that Alt a 1-induced immune responses were dependent upon toll-like receptors (TLRs) 2 and 4, and the adaptor proteins MYD88 and TIRAP. Studies utilizing human embryonic kidney cells engineered to express single receptors on the cell surface such as TLRs, further confirmed that Alt a 1-induced innate immunity is dependent upon TLR4 and to a lesser extent TLR2.
变应原是指在致敏个体中引发超敏炎症反应的分子,来源于多种来源。Alt a 1 是普遍存在的真菌的最重要的临床分泌性过敏原。它已被证明是引起绝大多数 - 致敏个体 IgE 介导的过敏反应的主要过敏原。然而,尚未对这种临床相关蛋白的先天免疫引发活性进行研究。在这项研究中,生产、纯化、标记了重组 Alt a 1,并与 BEAS-2B、NHBE 和 DHBE 人肺上皮细胞孵育。Alt a 1 强烈诱导了 IL-8、MCP-1 和 Gro-a/b/g 的产生。使用基因特异性 siRNA、阻断抗体和化学抑制剂(如 LPS-RS),确定 Alt a 1 诱导的免疫反应依赖于 Toll 样受体 (TLR) 2 和 4,以及衔接蛋白 MYD88 和 TIRAP。利用在细胞表面表达单个受体(如 TLR)的人胚肾细胞进行的研究进一步证实,Alt a 1 诱导的先天免疫依赖于 TLR4,并且在较小程度上依赖于 TLR2。