State Key Laboratory of Drug Research & Center of Pharmaceutics, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
University of Chinese Academy of Sciences, Beijing, China.
Nat Nanotechnol. 2021 Nov;16(11):1271-1280. doi: 10.1038/s41565-021-00972-7. Epub 2021 Sep 27.
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.
I 型干扰素(IFN)功能障碍可能导致肿瘤中的免疫缺陷。目前的补充 IFN 治疗部分恢复了抗癌免疫,但同时通过上调多个免疫检查点诱导免疫逃逸。在这里,我们创建了一种 T 淋巴细胞膜修饰的表观遗传纳米诱导剂,该诱导剂通过程序性细胞死亡蛋白 1(PD1)进行工程设计,我们称之为 OPEN,用于递送 IFN 诱导剂 ORY-1001。OPEN 增加了 IFNs 并阻止了 IFN 诱导的免疫检查点上调。OPEN 还通过 PDL1/PD1 识别靶向表达程序性死亡配体 1(PDL1)的肿瘤,随后触发 OPEN 和免疫检查点蛋白的内化。装载 ORY-1001 的 OPEN 上调了肿瘤内 IFNs 及其下游主要组织相容性复合体 I 和 PDL1。补充的 PDL1 使 OPEN 进一步结合,从而阻断 PDL1。这些连续的过程导致肿瘤内总和活性细胞毒性 T 淋巴细胞的密度分别增加了八倍和二十九倍,并强烈抑制了异种移植物肿瘤的生长。这种 T 淋巴细胞膜修饰的表观遗传纳米诱导剂为增强抗肿瘤免疫提供了一个可推广的平台。