免疫系统
表观遗传学
细胞毒性T细胞
免疫疗法
淋巴细胞
生物
癌症研究
抗原
免疫检查点
下调和上调
免疫
细胞生物学
免疫学
基因
遗传学
体外
作者
Yihui Zhai,Jinming Wang,Tianqun Lang,Ying Kong,Rong Rong,Ying Cai,Ran Wei,Fengqin Xiong,Chao Zheng,Wang Yanke,Yang Yu,Helen He Zhu,Pengcheng Zhang,Yaping Li
标识
DOI:10.1038/s41565-021-00972-7
摘要
Impaired type I interferons (IFNs) may cause immune deficiency in tumours. Current supplementary IFN therapy partially restores anticancer immunity but simultaneously induces immune evasion by upregulating multiple immune checkpoints. Here we create a T lymphocyte membrane-decorated epigenetic nanoinducer that is engineered with programmed cell death protein 1 (PD1), which we call OPEN, for the delivery of the IFN inducer ORY-1001. OPEN increases IFNs and blocks IFN-induced immune checkpoint upregulation. OPEN also targets tumours that express programmed cell death ligand 1 (PDL1) through PDL1/PD1 recognition and subsequently triggers the internalization of OPEN and immune checkpoint proteins. OPEN, which is loaded with ORY-1001, upregulates intratumoural IFNs and downstream major histocompatibility complex I and PDL1. The replenished PDL1 enables further ligation of OPEN, which in turn blocks PDL1. These sequential processes result in an eight- and 29-fold increase of the intratumoural densities of total and active cytotoxic T lymphocytes, respectively, and a strong inhibition of xenograft tumour growth. This T lymphocyte membrane-decorated epigenetic nanoinducer presents a generalizable platform to boost antitumour immunity.
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