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一种新型的NKG2D受体配体可激活自然杀伤细胞和巨噬细胞并诱导肿瘤免疫。

A novel ligand for the NKG2D receptor activates NK cells and macrophages and induces tumor immunity.

作者信息

Diefenbach Andreas, Hsia Jennifer K, Hsiung Ming-Yu B, Raulet David H

机构信息

Department of Molecular and Cell Biology, Cancer Research Laboratory, University of California, Berkeley 94720-3200, USA.

出版信息

Eur J Immunol. 2003 Feb;33(2):381-91. doi: 10.1002/immu.200310012.

Abstract

NK cells are involved in the immune response against viral and microbial infections and tumors. In contrast to B and T cells, NK cells employ various modes of immune recognition. An important mode of immune recognition employed by NK cells is "induced self recognition" exemplified by the NKG2D receptor-ligand system. The NKG2D immunoreceptor, expressed by NK cells, and by activated CD8+ T cells and macrophages, recognizes one of several cell surface ligands that are distantly related to MHC class I molecules (i.e. H60 and Rae1 proteins in mice, and MHC class I chain-related proteins and UL-16-binding proteins in humans). These ligands are not expressed abundantly by most normal cells but are up-regulated on cells exposed to various forms of cellular insults. Here we report the cloning of another ligand for NKG2D; transcripts of this ligand are found in a wide variety of tissues and in various tumor cells. Cross-linking of NKG2D with the novel ligand potently activated NK cells and macrophages. Tumor cells ectopically expressing the molecule were efficiently rejected by naive mice, and induced strong protective immunity to the parental, ligand-negative tumor cells.

摘要

自然杀伤细胞参与针对病毒、微生物感染及肿瘤的免疫反应。与B细胞和T细胞不同,自然杀伤细胞采用多种免疫识别模式。自然杀伤细胞所采用的一种重要免疫识别模式是以NKG2D受体 - 配体系统为代表的“诱导性自身识别”。自然杀伤细胞、活化的CD8 + T细胞和巨噬细胞表达的NKG2D免疫受体,可识别几种与MHC I类分子远缘相关的细胞表面配体之一(即小鼠中的H60和Rae1蛋白,以及人类中的MHC I类链相关蛋白和UL - 16结合蛋白)。这些配体在大多数正常细胞中表达不丰富,但在受到各种形式细胞损伤的细胞上会上调表达。在此我们报告了NKG2D的另一种配体的克隆;该配体的转录本存在于多种组织和各种肿瘤细胞中。NKG2D与这种新配体的交联能有效激活自然杀伤细胞和巨噬细胞。异位表达该分子的肿瘤细胞被未接触过抗原的小鼠有效排斥,并诱导对亲本的、配体阴性肿瘤细胞产生强烈的保护性免疫。

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