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IFN-γ-Induced Macrophage Antileishmanial Mechanisms in Mice: A Role for Immunity- Related GTPases Irgm1 and Irgm3 in Leishmania donovani Infection in the Liver

机译:IFN-γ诱导的小鼠巨噬细胞抗利什曼原虫机制:免疫相关的GTPases Irgm1和Irgm3在肝脏利什曼原虫感染中的作用

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摘要

In C57BL/6 mice, Leishmania donovani infection in the liver provoked IFN-γ induced expression of the immunity-related GTPases (IRG), Irgm1 and Irgm3. To gauge the antileishmanial effects of these macrophage factors in the liver, intracellular infection was analyzed in IRG-deficient mice. In early- (but not late-) stage infection, Irgm3−/− mice failed to properly control parasite replication, generated little tissue inflammation and were hyporesponsive to pentavalent antimony (Sb) chemotherapy. Observations limited to early-stage infection in Irgm1−/− mice demonstrated increased susceptibility and virtually no inflammatory cell recruitment to heavily-parasitized parenchymal foci but an intact response to chemotherapy. In L. donovani infection in the liver, the absence of either Irgm1 or Irgm3 impairs early inflammation and initial resistance; the absence of Irgm3, but not Irgm1, also appears to impair the intracellular efficacy of Sb chemotherapy.
机译:在C57BL / 6小鼠中,肝脏中的利什曼原虫感染引起了IFN-γ诱导免疫相关GTPases(IRG),Irgm1和Irgm3的表达。为了评估这些巨噬细胞因子在肝脏中的抗疟疾作用,在IRG缺陷型小鼠中分析了细胞内感染。在早期(但不是晚期)感染中,Irgm3 -/-小鼠未能正确控制寄生虫复制,几乎没有组织炎症,并且对五价锑(Sb)化疗反应低下。仅限于Irgm1 -/-小鼠早期感染的观察结果表明,易感性增加,几乎没有炎性细胞募集到高度寄生的实质性病灶,但对化学疗法的反应却完整。在肝脏的多诺氏乳杆菌感染中,缺少Irgm1或Irgm3会损害早期炎症和初始抵抗力。 Irgm3的缺失而不是Irgm1的缺失似乎也会损害Sb化疗的细胞内功效。

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