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Ixodes ricinus Salivary Serpin IRS-2 Affects Th17 Differentiation via Inhibition of the Interleukin-6/STAT-3 Signaling Pathway

机译:稻蓟马唾液丝氨酸蛋白酶抑制剂IRS-2通过抑制白介素6 / STAT-3信号通路影响Th17分化。

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摘要

Th17 cells constitute a subset of CD4+ T lymphocytes that play a crucial role in protection against extracellular bacteria and fungi. They are also associated with tissue injury in autoimmune and inflammatory diseases. Here, we report that serpin from the tick Ixodes ricinus, IRS-2, inhibits Th17 differentiation by impairment of the interleukin-6 (IL-6)/STAT-3 signaling pathway. Following activation, mature dendritic cells produce an array of cytokines, including the pleiotropic cytokine IL-6, which triggers the IL-6 signaling pathway. The major transcription factor activated by IL-6 is STAT-3. We show that IRS-2 selectively inhibits production of IL-6 in dendritic cells stimulated with Borrelia spirochetes, which leads to attenuated STAT-3 phosphorylation and finally to impaired Th17 differentiation. The results presented extend the knowledge about the effect of tick salivary serpins on innate immunity cells and their function in driving adaptive immune responses.
机译:Th17细胞是CD4 + T淋巴细胞的子集,在保护细胞外细菌和真菌中起着至关重要的作用。它们还与自身免疫和炎性疾病中的组织损伤有关。在这里,我们报告说,来自pin虱(Ixodes ricinus)IRS-2的丝氨酸蛋白酶抑制剂(serpin)通过白介素6(IL-6)/ STAT-3信号通路的损伤抑制Th17分化。激活后,成熟的树突状细胞产生一系列细胞因子,包括多效性细胞因子IL-6,这会触发IL-6信号通路。 IL-6激活的主要转录因子是STAT-3。我们表明,IRS-2选择性抑制在由疏螺旋体刺激的树突状细胞中产生IL-6,这导致STAT-3磷酸化减弱,并最终损害Th17分化。提出的结果扩展了关于of唾液丝氨酸蛋白酶抑制蛋白对先天免疫细胞的影响及其在驱动适应性免疫应答中的功能的知识。

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