Functions of NKG2D in CD8^(+) T cells: an opportunity for immunotherapy
作者机构:Loyola University ChicagoOncology InstituteMaywoodIL 60153USA
出 版 物:《Cellular & Molecular Immunology》 (中国免疫学杂志(英文版))
年 卷 期:2018年第15卷第5期
页 面:470-479页
核心收录:
学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学]
主 题:NKG2D CD28 CD8+T Cell Cancer Immunity Auto-immunity Memory Immunotherapy
摘 要:Natural killer group 2 member D(NKG2D)is a type II transmembrane ***2D is present on NK cells in both mice and humans,whereas it is constitutively expressed on CD8+T cells in humans but only expressed upon T-cell activation in ***2D is a promiscuous receptor that recognizes stress-induced surface *** NK cells,NKG2D signaling is sufficient to unleash the killing response;in CD8+T cells,this requires concurrent activation of the T-cell receptor(TCR).In this case,the function of NKG2D is to authenticate the recognition of a stressed target and enhance TCR ***28 has been established as an archetype provider of costimulation during T-cell *** has become apparent,however,that signals from other costimulatory receptors,such as NKG2D,are required for optimal T-cell function outside the priming *** review will focus on the similarities and differences between NKG2D and CD28;less well-described characteristics of NKG2D,such as the potential role of NKG2D in CD8+T-cell memory formation,cancer immunity and autoimmunity;and the opportunities for targeting NKG2D in immunotherapy.