Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Infect Immun. 2013 May;81(5):1420-9. doi: 10.1128/IAI.01301-12. Epub 2013 Feb 19.
Filarial infection is initiated by mosquito-derived third-stage larvae (L3) deposited on the skin that transit through the epidermis, which contains Langerhans cells (LC) and keratinocytes (KC), among other cells. This earliest interaction between L3 and the LC likely conditions the priming of the immune system to the parasite. To determine the nature of this interaction, human LC (langerin(+) E-cadherin(+) CD1a(+)) were generated in vitro and exposed to live L3. LC exposed to live L3 for 48 h showed no alterations in the cell surface markers CD14, CD86, CD83, CD207, E-cadherin, CD80, CD40, and HLA-DR or in mRNA expression of inflammation-associated genes, such as those for interleukin 18 (IL-18), IL-18BP, and caspase 1. In contrast to L3, live tachyzoites of Toxoplasma gondii, an intracellular parasite, induced production of CXCL9, IP-10, and IL-6 in LC. Furthermore, preexposure of LC to L3 did not alter Toll-like receptor 3 (TLR3)- or TLR4-mediated expression of the proinflammatory cytokines IL-1β, gamma interferon (IFN-γ), IL-6, or IL-10. Interestingly, cocultures of KC and LC produced significantly more IL-18, IL-1α, and IL-8 than did cultures of LC alone, although exposure of the cocultures to live L3 did not result in altered cytokine production. Microarray examination of ex vivo LC from skin blisters that were exposed to live L3 also showed few significant changes in gene expression compared with unexposed blisters, further underscoring the relatively muted response of LC to L3. Our data suggest that failure by LC to initiate an inflammatory response to the invasive stage of filarial parasites may be a strategy for immune evasion by the filarial parasite.
丝虫感染是由蚊子传播的第三期幼虫(L3)在皮肤上沉积引起的,这些幼虫穿过表皮,其中含有朗格汉斯细胞(LC)和角质形成细胞(KC)等细胞。L3 与 LC 之间的这种最早相互作用可能使免疫系统对寄生虫产生启动作用。为了确定这种相互作用的性质,体外生成了人类 LC(朗格汉斯蛋白(+)E-钙粘蛋白(+)CD1a(+)),并将其暴露于活的 L3 中。将 LC 暴露于活的 L3 中 48 小时后,细胞表面标记物 CD14、CD86、CD83、CD207、E-钙粘蛋白、CD80、CD40 和 HLA-DR 或炎症相关基因(如白细胞介素 18(IL-18)、IL-18BP 和半胱天冬酶 1)的 mRNA 表达均无改变。与 L3 相反,活的刚地弓形虫(一种细胞内寄生虫)滋养体诱导 LC 产生 CXCL9、IP-10 和 IL-6。此外,LC 预先暴露于 L3 不会改变 TLR3 或 TLR4 介导的促炎细胞因子 IL-1β、γ干扰素(IFN-γ)、IL-6 或 IL-10 的表达。有趣的是,与单独 LC 培养物相比,KC 和 LC 的共培养物产生的 IL-18、IL-1α 和 IL-8 明显更多,尽管将共培养物暴露于活的 L3 不会导致细胞因子产生改变。与未暴露的水疱相比,用活的 L3 暴露于皮肤水疱的 ex vivo LC 的微阵列检查显示基因表达变化很少,这进一步强调了 LC 对 L3 的反应相对较温和。我们的数据表明,LC 未能对丝虫寄生虫的侵袭阶段引发炎症反应可能是丝虫寄生虫免疫逃避的一种策略。