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深度学习引导的微流控用于肿瘤免疫治疗筛选

英文原题:Microfluidics guided by deep learning for cancer immunotherapy screening.

查看英文原题

Microfluidics guided by deep learning for cancer immunotherapy screening.

PubMed 2022/11/07(内容时间) Proc Natl Acad Sci U S A Q1 · IF 9.5(JCR 2025)

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中文摘要

免疫细胞浸润和细胞毒性在炎症和免疫治疗中均发挥关键作用。然而,目前癌症免疫治疗筛选方法忽略了T细胞穿透肿瘤间质的能力,显著限制了实体瘤有效疗法的开发。本文介绍一种自动化高通量微流控平台,可同时追踪T细胞在基质组成可调的三维肿瘤培养物中的浸润动态和细胞毒作用。平台借助基于临床数据深度学习方法开发的TIL(肿瘤浸润淋巴细胞)评分分析器,根据T细胞浸润模式评分,评估不同治疗的疗效。研究人员使用该技术筛选药物库,发现一种表观遗传药物——赖氨酸特异性组蛋白去甲基化酶1抑制剂(LSD1i)——可有效促进T细胞浸润肿瘤,并在体内与免疫检查点抑制剂抗PD-1联合后增强疗效。本研究展示了一种自动化筛选免疫细胞与实体瘤相互作用的系统和策略,可用于发现免疫疗法及联合疗法。

展开英文摘要原文

Immunocyte infiltration and cytotoxicity play critical roles in both inflammation and immunotherapy.

However, current cancer immunotherapy screening methods overlook the capacity of the T cells to penetrate the tumor stroma, thereby significantly limiting the development of effective treatments for solid tumors.

Here, we present an automated high-throughput microfluidic platform for simultaneous tracking of the dynamics of T cell infiltration and cytotoxicity within the 3D tumor cultures with a tunable stromal makeup. By recourse to a clinical tumor-infiltrating lymphocyte (TIL) score analyzer, which is based on a clinical data-driven deep learning method, our platform can evaluate the efficacy of each treatment based on the scoring of T cell infiltration patterns.

By screening a drug library using this technology, we identified an epigenetic drug (lysine-specific histone demethylase 1 inhibitor, LSD1i) that effectively promoted T cell tumor infiltration and enhanced treatment efficacy in combination with an immune checkpoint inhibitor (anti-PD1) in vivo.

We demonstrated an automated system and strategy for screening immunocyte-solid tumor interactions, enabling the discovery of immuno- and combination therapies.

论文信息

作者
Ao Z、Cai H、Wu Z、Hu L、Nunez A、Zhou Z、Liu H、Bondesson M
单位
Department of Intelligent Systems Engineering, Indiana University, Bloomington, IN 47405.
文献类型
非美国政府资助研究 · 美国 NIH 资助研究
期刊
Proceedings of the National Academy of Sciences of the United States of America2022 Nov 16
原文标识
PubMed 36343225 · DOI 10.1073/pnas.2214569119