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丙型肝炎病毒核心蛋白对 NK 细胞系 YTS 功能反应的影响。

The effects of hepatitis C virus core protein on functional responses in the NK cell line YTS.

机构信息

Department of Medicine, Center for Infectious Medicine, Huddinge University Hospital Karolinska Institute, Stockholm, Sweden.

出版信息

Scand J Immunol. 2012 Jan;75(1):54-60. doi: 10.1111/j.1365-3083.2011.02624.x.

Abstract

Hepatitis C virus infection affects more than 170 million people worldwide. More than 80% of the patients are not able to eliminate the virus and progress to a chronic infection that usually culminates in complications such as cirrhosis and/or hepatocellular carcinoma. Although the adaptive immune response has been widely shown to be essential for viral clearance, the role of natural killer (NK) cells is not clearly understood. In this study, the effect of HCV core protein is examined on NK cell function, i.e., cytotoxicity and cytokine secretion. The expression of core protein in the YTS NK cell line led to an increase in the percentage of apoptotic cells soon after transduction. The surviving cells exhibited decreased cytotoxicity associated with decreases in perforin and granzyme B expression. Furthermore, the HCV core protein-transduced YTS NK cells had reduced IFNγ production as well as an altered surface receptor expression pattern. These features may correspond to a state of functional anergy similar to that seen in T cells transduced with HCV core protein. Together, these data suggest that HCV core protein may alter NK cell function.

摘要

丙型肝炎病毒感染影响全球超过 1.7 亿人。超过 80%的患者无法清除病毒,进展为慢性感染,通常最终导致肝硬化和/或肝细胞癌等并发症。尽管适应性免疫反应已被广泛证明对病毒清除至关重要,但自然杀伤 (NK) 细胞的作用尚不清楚。在这项研究中,研究了丙型肝炎病毒核心蛋白对 NK 细胞功能(即细胞毒性和细胞因子分泌)的影响。YTS NK 细胞系中转录核心蛋白后,很快就会导致凋亡细胞的百分比增加。存活细胞表现出与穿孔素和颗粒酶 B 表达减少相关的细胞毒性降低。此外,HCV 核心蛋白转导的 YTS NK 细胞产生的 IFNγ 减少,表面受体表达模式发生改变。这些特征可能对应于与转导 HCV 核心蛋白的 T 细胞相似的功能无反应状态。总之,这些数据表明 HCV 核心蛋白可能改变 NK 细胞的功能。

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