School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
School of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Sci Adv. 2024 Aug 23;10(34):eado6566. doi: 10.1126/sciadv.ado6566.
XPO1 (Exportin-1/CRM1) is a nuclear export protein that is frequently overexpressed in cancer and functions as a driver of oncogenesis. Currently small molecules that target XPO1 are being used in the clinic as anticancer agents. We identify XPO1 as a target for natural killer (NK) cells. Using immunopeptidomics, we have identified a peptide derived from XPO1 that can be recognized by the activating NK cell receptor KIR2DS2 in the context of human leukocyte antigen-C. The peptide can be endogenously processed and presented to activate NK cells specifically through this receptor. Although high XPO1 expression in cancer is commonly associated with a poor prognosis, we show that the outcome of specific cancers, such as hepatocellular carcinoma, can be substantially improved if there is concomitant evidence of NK cell infiltration. We thus identify XPO1 as a bona fide tumor antigen recognized by NK cells that offers an opportunity for a personalized approach to NK cell therapy for solid tumors.
XPO1(Exportin-1/CRM1)是一种核输出蛋白,在癌症中经常过表达,是致癌作用的驱动因素。目前,靶向 XPO1 的小分子正被用于临床作为抗癌药物。我们确定 XPO1 是自然杀伤 (NK) 细胞的靶点。通过免疫肽组学,我们已经鉴定出一种来源于 XPO1 的肽,它可以在人类白细胞抗原-C 的背景下被激活 NK 细胞受体 KIR2DS2 识别。该肽可以被内源性加工并呈递给激活 NK 细胞,特异性地通过该受体。尽管癌症中高 XPO1 表达通常与预后不良相关,但我们表明,如果有 NK 细胞浸润的证据,特定癌症(如肝细胞癌)的结局可以得到显著改善。因此,我们确定 XPO1 是 NK 细胞识别的真正肿瘤抗原,为 NK 细胞治疗实体瘤提供了个性化方法的机会。