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CXC趋化因子配体10控制中枢神经系统中的病毒感染:通过募集和激活自然杀伤细胞在先天免疫反应中发挥作用的证据。

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.

作者信息

Trifilo Matthew J, Montalto-Morrison Cynthia, Stiles Linda N, Hurst Kelley R, Hardison Jenny L, Manning Jerry E, Masters Paul S, Lane Thomas E

机构信息

Department of Molecular Biology and Biochemistry, University of California, Irvine, California 92697-3900, USA.

出版信息

J Virol. 2004 Jan;78(2):585-94. doi: 10.1128/jvi.78.2.585-594.2004.

Abstract

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.

摘要

趋化因子如何塑造针对中枢神经系统(CNS)病毒感染的免疫反应,很大程度上是在抗原特异性淋巴细胞的募集和激活背景下进行考虑的。然而,趋化因子在病毒感染后早期就会表达,这表明其在协调先天性免疫反应中发挥重要作用。在此,我们评估了CXC趋化因子配体10(CXCL10)在促进中枢神经系统冠状病毒感染后先天性防御机制中的作用。用表达重组CXCL10的鼠冠状病毒(小鼠肝炎病毒)对RAG1(-/-)小鼠进行脑内感染,结果显示可预防疾病并提高存活率,这与中枢神经系统内自然杀伤(NK)细胞的募集和激活显著增加相关。NK细胞的积累导致病毒滴度降低,这依赖于γ干扰素的分泌。这些结果表明,CXCL10的表达通过增强先天性免疫反应,在中枢神经系统冠状病毒感染后的防御中起关键作用。

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