细胞毒性T细胞
抗原
免疫系统
癌症研究
内体
热休克蛋白90
肿瘤抗原
细胞生物学
化学
癌症免疫疗法
基因敲除
免疫
生物
CDC37型
免疫检查点
免疫疗法
抗原提呈细胞
树突状细胞
癌细胞
激酶
胞浆
交叉展示
封锁
癌症
抗原呈递
T细胞
免疫学
获得性免疫系统
抗体
CD8型
细胞外
作者
Ruxin Wang,YunYi Zhang,Xiangyu Meng,Jianli Zhao,Yue Xing,Qian Ouyang,Ning Zhang,Huiping Chen,Nanyan Miao,Erwei Song,Di Huang
标识
DOI:10.1002/advs.202506518
摘要
Abstract Tumor mutational burden (TMB), usually representing high immunogenicity, cannot always predict treatment response of immune checkpoint blockade (ICB). Here, it is showed that defective antigen cross‐presentation in type 1 conventional dendritic cells (cDC1) is responsible for lacking tumor‐specific cytotoxic T lymphocytes (CTLs) in triple‐negative breast cancer (TNBC) patients. Mechanistically, tumor cytosolic CDC37, shuttled via extracellular vesicles (EVs) into the endosomes of intratumor dendritic cells (DCs), inhibits antigen cross‐presentation by locking antigen binding to HSP90 and precluding their translocation from endosomes to cytoplasm. CDC37 knockdown in tumor cells or inhibiting CDC37/HSP90 interaction in DCs efficiently promotes antigen translocation and enhances their cross‐presentation, which improves ICB therapeutic responses. Clinically, high tumor CDC37 expression is associated with low infiltration of antigen‐specific CTLs and poor ICB efficacy in TNBC patients. Therefore, tumor EV‐shuttled CDC37 locks antigen/chaperone interaction and impairs antigen cross‐presentation in DCs. Moreover, targeting CDC37 is promising to enhance anti‐tumor immunity and reverse ICB resistance.
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