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Natural killer cell activation enhances immune pathology and promotes chronic infection by limiting CD8+ T-cell immunity

机译:通过限制CD8 + T细胞免疫力,自然杀伤细胞激活增强免疫病理并促进慢性感染

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摘要

Infections with HIV, hepatitis B virus, and hepatitis C virus can turn into chronic infections, which currently affect more than 500 million patients worldwide. It is generally thought that virus-mediated T-cell exhaustion limits T-cell function, thus promoting chronic disease. Here we demonstrate that natural killer (NK) cells have a negative impact on the development of T-cell immunity by using the murine lymphocytic choriomeningitis virus. NK cell-deficient (Nfil3−/−, E4BP4−/−) mice exhibited a higher virus-specific T-cell response. In addition, NK cell depletion caused enhanced T-cell immunity in WT mice, which led to rapid virus control and prevented chronic infection in lymphocytic choriomeningitis virus clone 13- and reduced viral load in DOCILE-infected animals. Further experiments showed that NKG2D triggered regulatory NK cell functions, which were mediated by perforin, and limited T-cell responses. Therefore, we identified an important role of regulatory NK cells in limiting T-cell immunity during virus infection.
机译:感染艾滋病毒,乙型肝炎病毒和丙型肝炎病毒可转变为慢性感染,目前影响全球5亿多患者。通常认为病毒介导的T细胞衰竭限制了T细胞功能,从而促进了慢性疾病。在这里,我们证明了自然杀手(NK)细胞通过使用鼠淋巴细胞性脉络膜脑膜炎病毒对T细胞免疫的发展具有负面影响。 NK细胞缺陷(Nfil3-/-,E4BP4-/-)小鼠表现出更高的病毒特异性T细胞应答。此外,NK细胞耗竭可导致WT小鼠的T细胞免疫增强,从而导致病毒快速控制并防止了淋巴细胞性脉络膜脑膜炎病毒克隆13的慢性感染,并减少了DOCILE感染动物的病毒载量。进一步的实验表明,NKG2D触发了由穿孔素介导的调节性NK细胞功能和有限的T细胞反应。因此,我们确定了病毒感染过程中调节性NK细胞在限制T细胞免疫中的重要作用。

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