Cancer Immunotherapy Therapeutic Manipulation of the CD8-HLA Class I Interaction: Potential and Challenges

P. Savage
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引用次数: 3

Abstract

The interaction between CD8 and HLA class I is largely monomorphic and of low affinity. Previous studies have indicated that changing the affinity of this interaction can have dramatic biological effects. Reductions in CD8-HLA class I binding affinity can lead to inhibition of T cell mediated target cell killing, whilst modest affinity increases lead to enhanced target cell killing with retained antigenic specificity. Here it is shown that target cells bearing a high affinity chimeric MHC molecule termed a ‘Supertarget’ comprising the HLA-A2 molecule incorporating the murine MHC Kb alpha 3 domain can be killed by T cells irrespective of their native HLA or peptide specificity. We will review the immunotherapy potential of this Supertarget protein and also how novel drugs acting as agonists or antagonists at the CD8-HLA class I interface could have clinical potential.
癌症免疫疗法对CD8-HLA I类相互作用的治疗操作:潜力和挑战
CD8和HLA I类之间的相互作用在很大程度上是单态的和低亲和力的。先前的研究表明,改变这种相互作用的亲和力可以产生戏剧性的生物学效应。CD8-HLA I类结合亲和力的降低可以抑制T细胞介导的靶细胞杀伤,而适度的亲和力增加可以增强靶细胞杀伤,同时保留抗原特异性。这里的研究表明,靶细胞具有高亲和力嵌合MHC分子,称为“超级靶标”,包含含有小鼠MHC Kb α 3结构域的HLA- a2分子,无论其天然HLA或肽特异性如何,都可以被T细胞杀死。我们将回顾这种超靶蛋白的免疫治疗潜力,以及在CD8-HLA I类界面上作为激动剂或拮抗剂的新药如何具有临床潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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