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肝脏中 NK 细胞的关键特征和归巢特性是由激活的 iNKT 细胞塑造的。

Key features and homing properties of NK cells in the liver are shaped by activated iNKT cells.

机构信息

Department of Vaccinology and Applied Microbiology, Helmholtz Centre for Infection Research, D-38124, Braunschweig, Germany.

Center for Infectious Medicine, Department of Medicine, Karolinska Institute, Karolinska University Hospital Huddinge, Stockholm, S-14186, Sweden.

出版信息

Sci Rep. 2019 Nov 8;9(1):16362. doi: 10.1038/s41598-019-52666-9.

Abstract

The contribution of natural killer (NK) cells to the clearance of hepatic viral infections is well recognized. The recently discovered heterogeneity of NK cell populations renders them interesting targets for immune interventions. Invariant natural killer T (iNKT) cells represent a key interaction partner for hepatic NK cells. The present study addressed whether characteristics of NK cells in the liver can be shaped by targeting iNKT cells. For this, the CD1d-binding pegylated glycolipid αGalCerMPEG was assessed for its ability to modulate the features of NK cells permanently or transiently residing in the liver. In vivo administration resulted in enhanced functionality of educated and highly differentiated CD27 Mac-1 NK cells accompanied by an increased proliferation. Improved liver homing was supported by serum-derived and cellular factors. Reduced viral loads in a mCMV infection model confirmed the beneficial effect of NK cells located in the liver upon stimulation with αGalCerMPEG. Thus, targeting iNKT cell-mediated NK cell activation in the liver represents a promising approach for the establishment of liver-directed immune interventions.

摘要

自然杀伤 (NK) 细胞对清除肝脏病毒感染的贡献已得到广泛认可。最近发现 NK 细胞群体存在异质性,这使得它们成为免疫干预的有趣靶点。恒定自然杀伤 T(iNKT) 细胞是 NK 细胞在肝脏中的主要相互作用伙伴。本研究旨在探讨针对 iNKT 细胞是否可以改变肝脏 NK 细胞的特征。为此,评估了 CD1d 结合聚乙二醇化糖脂αGalCerMPEG 永久性或短暂性调节肝脏中固有 NK 细胞特征的能力。体内给药导致具有教育意义的和高度分化的 CD27 Mac-1 NK 细胞的功能增强,同时伴有增殖增加。血清衍生和细胞因子支持改善的肝脏归巢。在 mCMV 感染模型中降低病毒载量证实了刺激αGalCerMPEG 后位于肝脏中的 NK 细胞的有益作用。因此,针对 iNKT 细胞介导的 NK 细胞在肝脏中的激活代表了建立肝脏定向免疫干预的一种有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2c4/6841958/e2ced889bf57/41598_2019_52666_Fig1_HTML.jpg

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