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IFN-gamma-induced macrophage antileishmanial mechanisms in mice: A role for immunity-related GTPases, Irgm1 and Irgm3, in Leishmania donovani infection in the liver

机译:干扰素-γ诱导的小鼠巨噬细胞反噬机制: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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In C57BL/6 mice, Leishmania donovani infection in the liver provoked IFN-gamma-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. (C) 2015 Elsevier Inc. All rights reserved.
机译:在C57BL / 6小鼠中,肝脏中的利什曼原虫多巴尼病毒感染引起了IFN-γ诱导的免疫相关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,几乎没有组织发炎,并且对五价锑(Sb)化疗反应低下。仅限于Irgm1(-/-)小鼠的早期感染的观察结果表明,易感性增加,几乎没有炎症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好。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。 (C)2015 Elsevier Inc.保留所有权利。

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