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Myd88-Dependent In Vivo Maturation of Splenic Dendritic Cells Induced by Leishmania donovani and Other Leishmania Species

机译:利什曼原虫和其他利什曼原虫物种诱导的脾脏树突状细胞的Myd88依赖性体内成熟

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摘要

The usual agent of visceral leishmaniasis in the Old World is Leishmania donovani, which typically produces systemic diseases in humans and mice. L. donovani has developed efficient strategies to infect and persist in macrophages from spleen and liver. Dendritic cells (DC) are sentinels of the immune system. Following recognition of evolutionary conserved microbial products, DC undergo a maturation process and activate antigen-specific naïve T cells. In the present report we provide new insights into how DC detect Leishmania in vivo. We demonstrate that in both C57BL/6 and BALB/c mice, systemic injection of L. donovani induced the migration of splenic DC from marginal zones to T-cell areas. During migration, DC upregulated the expression of major histocompatibility complex II and costimulatory receptors (such as CD40, CD80, and CD86). Leishmania-induced maturation requires live parasites and is not restricted to L. donovani, as L. braziliensis, L. major, and L. mexicana induced a similar process. Using a green fluorescent protein-expressing parasite, we demonstrate that DC undergoing maturation in vivo display no parasite internalization. We also show that L. donovani-induced DC maturation was partially abolished in MyD88-deficient mice. Taken together, our data suggest that Leishmania-induced DC maturation results from direct recognition of Leishmania by DC, and not from DC infection, and that MyD88-dependent receptors are implicated in this process.
机译:在旧世界,内脏利什曼病的常见病原是利什曼原虫,它通常在人和小鼠中引起全身性疾病。 L. donovani已开发出有效的策略来感染并持续存在于脾脏和肝脏的巨噬细胞中。树突状细胞(DC)是免疫系统的前哨。在认识到进化上保守的微生物产物后,DC经历了成熟过程并激活了抗原特异性幼稚T细胞。在本报告中,我们提供有关DC如何在体内检测利什曼原虫的新见解。我们证明,在C57BL / 6和BALB / c小鼠中,全身注射L. donovani诱导脾脏DC从边缘区迁移到T细胞区域。在迁移过程中,DC上调了主要组织相容性复合体II和共刺激受体(例如CD40,CD80和CD86)的表达。利什曼原虫诱导的成熟需要活的寄生虫,并且不限于杜氏乳杆菌,因为巴西乳杆菌,大乳杆菌和墨西哥乳杆菌也诱导了类似的过程。使用表达绿色荧光蛋白的寄生虫,我们证明DC在体内进行成熟显示没有寄生虫内在化。我们还显示,在MyD88缺陷型小鼠中,杜氏乳杆菌诱导的DC成熟被部分消除。两者合计,我们的数据表明,利什曼原虫诱导的DC成熟是由DC直接识别利什曼原虫引起的,而不是DC感染引起的,并且MyD88依赖性受体与该过程有关。

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