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Uncompromised NK cell activation is essential for virus-specific CTL activity during acute influenza virus infection

机译:在急性流感病毒感染期间毫不妥协的NK细胞活化对于病毒特异性CTL活性至关重要

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摘要

Natural killer (NK) cells are indispensable components of both the innate and adaptive immune response. However, their precise roles in the cross-talk between innate and adaptive immunity during influenza virus infection remain controversial. By comparing NK cell dynamics and activity under a sub-lethal dose and high dose of influenza virus infection, we showed that influenza virus PR8 directly infected NK cells during natural infection, which was consistent with our previous findings obtained from an in vitro investigation of human NK cells. The impairments in cytotoxicity and IFN-γ production by spleen NK cells following high-dose infection were accompanied by decreased virus-specific killing mediated by cytotoxic T lymphocytes (CTLs). Importantly, the weakened CTL activity could be reversed by adoptive transfer of spleen NK cells harvested from low-dose-infected mice but not healthy donors. Taken together, our data provide direct evidence supporting the contribution of NK cells to antiviral T-cell responses. This study also indicates that a novel NK-targeted immune evasion strategy is used by influenza virus to shrink both innate and adaptive immune responses.
机译:天然杀伤细胞(NK)是先天性和适应性免疫反应必不可少的组成部分。然而,它们在流感病毒感染过程中先天免疫与适应性免疫之间的相互作用中的确切作用仍存在争议。通过比较亚致死剂量和高剂量流感病毒感染下的NK细胞动力学和活性,我们显示流感病毒PR8在自然感染期间直接感染了NK细胞,这与我们先前从人体体外研究中获得的发现是一致的NK细胞。大剂量感染后,脾NK细胞对细胞毒性和IFN-γ产生的损害伴随着由细胞毒性T淋巴细胞(CTL)介导的病毒特异性杀伤力的降低。重要的是,通过从低剂量感染小鼠而非健康供体中收获的脾NK细胞过继转移,可以逆转减弱的CTL活性。两者合计,我们的数据提供直接的证据支持NK细胞对抗病毒T细胞反应的贡献。这项研究还表明,流感病毒使用一种新颖的针对NK的免疫逃避策略来缩小先天和适应性免疫应答。

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