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Topical application of the quaternary ammonium compound didecyldimethylammonium chloride activates type 2 innate lymphoid cells and initiates a mixed-type allergic response

机译:季铵化合物二癸基二甲基氯化铵的局部应用可激活2型先天淋巴样细胞并引发混合型变态反应

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摘要

Didecyldimethylammonium chloride (DDAC) is an antimicrobial dialkyl-quaternary ammonium compound used in industrial and commercial products. Clinical data suggest that DDAC exposure elicits multiple types of hypersensitivity reactions; here, we confirm this observation in a BALB/c murine model. To examine the immunological mechanism behind this mixed-type response and the potential involvement of type 2 innate lymphoid cells (ILC2s), we assessed early immune responses in the skin following topical DDAC exposure (0.125% and 0.5%). DDAC exposure resulted in a rapid and dramatic increase in the Th2-skewing and ILC2 activating cytokine thymic stromal lymphopoietin. Correspondingly, dermal ILC2s were activated 24 hours after DDAC exposure, resulting in increased expression of CD25, ICOS and KLRG1, and decreased CD127 throughout 7 days of exposure. Following ILC2 activation, the Th2 cytokine IL-4 was elevated compared to control mice in total ear protein lysate (0.5% DDAC). Rag2−/− mice were used to determine a functional role for ILC2s in DDAC induced sensitization. ILC2s from Rag2−/− mice were similarly activated by DDAC and, importantly, produced significant levels of IL-4 and IL-5 in the skin (0.5% DDAC). These data indicate that ILC2s contribute to early Th2 immune responses following DDAC exposure. ILC2s have been previously implicated in allergic responses, but to our knowledge have not been thoroughly investigated in chemical sensitization. These results indicate that following DDAC exposure, skin ILC2s become activated and produce Th2 cytokines, providing a possible mechanism for the development of the mixed-type allergic responses commonly observed with chemical sensitizers.
机译:十二烷基二甲基氯化铵(DDAC)是用于工业和商业产品的抗菌二烷基季铵盐化合物。临床数据表明,DDAC暴露会引起多种类型的超敏反应。在这里,我们在BALB / c鼠模型中证实了这一观察结果。为了检查这种混合型应答和2型先天性淋巴样细胞(ILC2s)潜在参与的免疫机制,我们评估了局部DDAC暴露后皮肤中的早期免疫应答(0.125%和0.5%)。 DDAC暴露导致Th2偏斜和ILC2激活细胞因子胸腺基质淋巴细胞生成素的急剧增加。相应地,真皮ILC2s在DDAC暴露后24小时被激活,导致CD25,ICOS和KLRG1的表达增加,并且在暴露的7天中CD127减少。在ILC2激活后,总耳蛋白裂解液(0.5%DDAC)中的Th2细胞因子IL-4与对照小鼠相比升高。使用Rag2 -/-小鼠确定ILC2在DDAC诱导的致敏中的功能作用。来自Rag2 -/-小鼠的ILC2同样被DDAC激活,重要的是,在皮肤中产生了显着水平的IL-4和IL-5(0.5%DDAC)。这些数据表明,ILC2有助于DDAC暴露后早期Th2免疫应答。 ILC2s以前曾涉及过敏反应,但据我们所知,尚未在化学致敏方面进行彻底研究。这些结果表明,在DDAC暴露后,皮肤ILC2被激活并产生Th2细胞因子,这为化学敏化剂常见的混合型过敏反应的发展提供了可能的机制。

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