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激活 NKG2C 受体:功能特征及临床应用中的当前策略。

Activating NKG2C Receptor: Functional Characteristics and Current Strategies in Clinical Applications.

机构信息

Laboratory of Clinical Immunogenetics and Pharmacogenetics, Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wroclaw, Poland.

Department of Biosensors and Processing of Biomedical Signals, Faculty of Biomedical Engineering, Silesian University of Technology, Zabrze, Poland.

出版信息

Arch Immunol Ther Exp (Warsz). 2023 Mar 10;71(1):9. doi: 10.1007/s00005-023-00674-z.

Abstract

The interest in NK cells and their cytotoxic activity against tumour, infected or transformed cells continuously increases as they become a new efficient and off-the-shelf agents in immunotherapies. Their actions are balanced by a wide set of activating and inhibitory receptors, recognizing their complementary ligands on target cells. One of the most studied receptors is the activating CD94/NKG2C molecule, which is a member of the C-type lectin-like family. This review is intended to summarise latest research findings on the clinical relevance of NKG2C receptor and to examine its contribution to current and potential therapeutic strategies. It outlines functional characteristics and molecular features of CD94/NKG2C, its interactions with HLA-E molecule and presented antigens, pointing out a key role of this receptor in immunosurveillance, especially in the human cytomegalovirus infection. Additionally, the authors attempt to shed some light on receptor's unique interaction with its ligand which is shared with another receptor (CD94/NKG2A) with rather opposite properties.

摘要

自然杀伤 (NK) 细胞及其对肿瘤、感染或转化细胞的细胞毒性作用引起了人们越来越多的兴趣,因为它们成为免疫治疗中一种新的有效且现成的药物。其作用受到一系列广泛的激活和抑制受体的平衡,这些受体识别靶细胞上互补的配体。研究最多的受体之一是激活的 CD94/NKG2C 分子,它是 C 型凝集素样家族的成员。这篇综述旨在总结 NKG2C 受体的最新临床相关性研究结果,并研究其对当前和潜在治疗策略的贡献。它概述了 CD94/NKG2C 的功能特征和分子特征,及其与 HLA-E 分子和呈递抗原的相互作用,指出了该受体在免疫监视中的关键作用,特别是在人类巨细胞病毒感染中。此外,作者试图阐明该受体与另一个受体(CD94/NKG2A)独特的相互作用,该受体与具有相反特性的配体共享。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3812/10006277/083f152e1d13/5_2023_674_Fig1_HTML.jpg

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