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CXC Chemokine Ligand 10 Controls Viral Infection in the Central Nervous System: Evidence for a Role in Innate Immune Response through Recruitment and Activation of Natural Killer Cells

机译:CXC趋化因子配体10控制中枢神经系统中的病毒感染:通过招募和激活自然杀伤细胞在先天免疫反应中的作用的证据。

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摘要

How chemokines shape the immune response to viral infection of the central nervous system (CNS) has largely been considered within the context of recruitment and activation of antigen-specific lymphocytes. However, chemokines are expressed early following viral infection, suggesting an important role in coordinating innate immune responses. Herein, we evaluated the contributions of CXC chemokine ligand 10 (CXCL10) in promoting innate defense mechanisms following coronavirus infection of the CNS. Intracerebral infection of RAG1−/− mice with a recombinant CXCL10-expressing murine coronavirus (mouse hepatitis virus) resulted in protection from disease and increased survival that correlated with a significant increase in recruitment and activation of natural killer (NK) cells within the CNS. Accumulation of NK cells resulted in a reduction in viral titers that was dependent on gamma interferon secretion. These results indicate that CXCL10 expression plays a pivotal role in defense following coronavirus infection of the CNS by enhancing innate immune responses.
机译:在募集和激活抗原特异性淋巴细胞的背景下,已经广泛考虑了趋化因子如何形成对中枢神经系统(CNS)病毒感染的免疫反应。然而,趋化因子在病毒感染后早期表达,提示在协调先天免疫应答中的重要作用。在本文中,我们评估了冠状病毒感染中枢神经系统后CXC趋化因子配体10(CXCL10)在促进先天防御机制中的作用。用重组表达CXCL10的鼠冠状病毒(小鼠肝炎病毒)对RAG1-/-小鼠进行脑内感染可预防疾病,并延长生存期,这与CNS内自然杀伤(NK)细胞的募集和激活显着增加有关。 NK细胞的积累导致病毒滴度降低,这取决于γ干扰素的分泌。这些结果表明CXCL10表达在冠状病毒感染中枢神经系统后通过增强先天免疫应答在防御中起关键作用。

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