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肿瘤免疫中的NKG2D配体

NKG2D ligands in tumor immunity.

作者信息

Nausch N, Cerwenka A

机构信息

Division of Innate Immunity, German Cancer Research Center, Im Neuenheimer Feld 280, Heidelberg, Germany.

出版信息

Oncogene. 2008 Oct 6;27(45):5944-58. doi: 10.1038/onc.2008.272.

Abstract

The activating receptor NKG2D (natural-killer group 2, member D) and its ligands play an important role in the NK, gammadelta(+) and CD8(+) T-cell-mediated immune response to tumors. Ligands for NKG2D are rarely detectable on the surface of healthy cells and tissues, but are frequently expressed by tumor cell lines and in tumor tissues. It is evident that the expression levels of these ligands on target cells have to be tightly regulated to allow immune cell activation against tumors, but at the same time avoid destruction of healthy tissues. Importantly, it was recently discovered that another safeguard mechanism controlling activation via the receptor NKG2D exists. It was shown that NKG2D signaling is coupled to the IL-15 receptor pathway in a cell-specific manner suggesting that priming of NKG2D-mediated activation depends on the cellular microenvironment and the distinct cellular context. This review will provide a broad overview of our up-to-date knowledge of the NKG2D receptor and its ligands in the context of tumor immunology. Strategies to amplify NKG2D-mediated antitumor responses and counteract tumor immune escape mechanisms will be discussed.

摘要

激活受体NKG2D(自然杀伤细胞2族D成员)及其配体在自然杀伤细胞、γδ(+)和CD8(+) T细胞介导的肿瘤免疫反应中发挥重要作用。NKG2D的配体在健康细胞和组织表面很少能检测到,但在肿瘤细胞系和肿瘤组织中经常表达。显然,这些配体在靶细胞上的表达水平必须受到严格调控,以允许免疫细胞激活来对抗肿瘤,同时避免对健康组织的破坏。重要的是,最近发现存在另一种通过受体NKG2D控制激活的保障机制。研究表明,NKG2D信号以细胞特异性方式与白细胞介素-15受体途径偶联,这表明NKG2D介导的激活启动取决于细胞微环境和独特的细胞背景。本综述将全面概述我们目前在肿瘤免疫学背景下对NKG2D受体及其配体的认识。还将讨论增强NKG2D介导的抗肿瘤反应和对抗肿瘤免疫逃逸机制的策略。

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