肿瘤微环境
生物
多路复用
人口
免疫疗法
计算生物学
模式
免疫系统
判别式
桥接(联网)
生物信息学
癌症
人工智能
癌症免疫疗法
数字化病理学
细胞
癌症研究
模态(人机交互)
虚拟病人
计算机科学
机器学习
肿瘤浸润淋巴细胞
免疫学
H&E染色
作者
Jeya Maria Jose Valanarasu,Hanwen Xu,Naoto Usuyama,Chanwoo Kim,Cliff Wong,Peniel Argaw,Racheli Ben Shimol,Angela Crabtree,Kevin Matlock,Alexandra Q. Bartlett,Jaspreet Bagga,裕二 池谷,Sheng Zhang,Tristan Naumann,Bernard A. Fox,Bill Wright,Ari Robicsek,Brian Piening,Carlo Bifulco,Sheng Wang
出处
期刊:Cell
[Cell Press]
日期:2025-12-09
卷期号:189 (2): 386-400.e19
被引量:31
标识
DOI:10.1016/j.cell.2025.11.016
摘要
The tumor immune microenvironment (TIME) critically impacts cancer progression and immunotherapy response. Multiplex immunofluorescence (mIF) is a powerful imaging modality for deciphering TIME, but its applicability is limited by high cost and low throughput. We propose GigaTIME, a multimodal AI framework for population-scale TIME modeling by bridging cell morphology and states. GigaTIME learns a cross-modal translator to generate virtual mIF images from hematoxylin and eosin (H&E) slides by training on 40 million cells with paired H&E and mIF data across 21 proteins. We applied GigaTIME to 14,256 patients from 51 hospitals and over 1,000 clinics across seven US states in Providence Health, generating 299,376 virtual mIF slides spanning 24 cancer types and 306 subtypes. This virtual population uncovered 1,234 statistically significant associations linking proteins, biomarkers, staging, and survival. Such analyses were previously infeasible due to the scarcity of mIF data. Independent validation on 10,200 TCGA patients further corroborated our findings.
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