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Persistently Active Microbial Molecules Prolong Innate Immune Tolerance In Vivo

机译:持久活性微生物分子可延长体内的先天免疫耐受性

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摘要

Measures that bolster the resolution phase of infectious diseases may offer new opportunities for improving outcome. Here we show that inactivation of microbial lipopolysaccharides (LPS) can be required for animals to recover from the innate immune tolerance that follows exposure to Gram-negative bacteria. When wildtype mice are exposed to small parenteral doses of LPS or Gram-negative bacteria, their macrophages become reprogrammed (tolerant) for a few days before they resume normal function. Mice that are unable to inactivate LPS, in contrast, remain tolerant for several months; during this time they respond sluggishly to Gram-negative bacterial challenge, with high mortality. We show here that prolonged macrophage reprogramming is maintained in vivo by the persistence of stimulatory LPS molecules within the cells' in vivo environment, where naïve cells can acquire LPS via cell-cell contact or from the extracellular fluid. The findings provide strong evidence that inactivation of a stimulatory microbial molecule can be required for animals to regain immune homeostasis following parenteral exposure to bacteria. Measures that disable microbial molecules might enhance resolution of tissue inflammation and help restore innate defenses in individuals recovering from many different infectious diseases.
机译:支持传染病解决阶段的措施可能会为改善结果提供新的机会。在这里,我们表明,动物要从暴露于革兰氏阴性细菌后的先天免疫耐受中恢复过来,可能需要使微生物脂多糖(LPS)失活。当野生型小鼠暴露于小剂量肠胃外的LPS或革兰氏阴性细菌时,它们的巨噬细胞在重新恢复正常功能前几天会被重新编程(耐受)。相比之下,不能灭活LPS的小鼠可以耐受几个月。在这段时间内,他们对革兰氏阴性细菌的攻击反应迟钝,死亡率很高。我们在这里显示通过在体内环境中刺激性LPS分子的持续存在,在体内可以维持延长的巨噬细胞重编程,在该环境中,幼稚细胞可以通过细胞与细胞的接触或从细胞外液中获得LPS。这些发现提供了有力的证据,证明动物肠胃外暴露于细菌后,可能需要使微生物分子失活才能恢复免疫稳态。禁用微生物分子的措施可能会增强组织炎症的分辨率,并有助于恢复从许多不同传染病中康复的个体的先天防御能力。

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