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Cutting Edge: IL-12 Is Required for the Maintenance of IFN-γ Production in T Cells Mediating Chronic Resistance to the Intracellular Pathogen, Toxoplasma gondii

机译:前沿:IL-12是维持介导对细胞内病原体弓形虫慢性耐药的T细胞中IFN-γ产生的维持所必需的

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IL-12 is required for the development of IFN-γ-dependent resistance to intracellular pathogens but is not thought to play a major role in its maintenance. To directly assess the requirement for continuous IL-12 signaling in long-term cell-mediated immunity, recombinant cytokine was transiently administered to IL-12 p40-deficient mice during the first 2 wk of infection with the intracellular pathogen Toxoplasma gondii . As expected, these animals survived the acute phase and established chronic infections. However, 4–6 wk after IL-12 withdrawal, the mice exhibited increased brain cyst burdens and succumbed to toxoplasmic encephalitis. Reactivation was associated with a loss of T-dependent IFN-γ production without a concomitant increase in Th2 cytokine expression. Importantly, parasite Ag-induced IFN-γ synthesis by purified T cells from these animals could be restored by in vitro exposure to IL-12. These results argue that endogenous IL-12 is required for the long-term maintenance of IFN-γ-dependent resistance against intracellular pathogens.
机译:IL-12是发展对细胞内病原体的IFN-γ依赖性抗性所必需的,但认为在其维持中不发挥主要作用。为了直接评估在长期细胞介导的免疫中持续IL-12信号传导的需求,在细胞内病原体弓形虫感染的前两周内,向IL-12 p40缺陷型小鼠瞬时给予重组细胞因子。正如预期的那样,这些动物在急性期幸存下来并建立了慢性感染。然而,在IL-12撤离后4-6周,小鼠表现出增加的脑囊肿负担并屈服于弓形体性脑炎。重新激活与T依赖性IFN-γ产生的损失相关,而Th2细胞因子表达却没有随之增加。重要的是,可以通过体外暴露于IL-12恢复来自这些动物的纯化T细胞的寄生虫Ag诱导的IFN-γ合成。这些结果表明,内源性IL-12是长期维持对细胞内病原体的IFN-γ依赖性耐药所必需的。

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