Author:
Cuccarese Michael F.,Earnshaw Berton A.,Heiser Katie,Fogelson Ben,Davis Chadwick T.,McLean Peter F.,Gordon Hannah B.,Skelly Kathleen-Rose,Weathersby Fiona L.,Rodic Vlad,Quigley Ian K.,Pastuzyn Elissa D.,Mendivil Brandon M.,Lazar Nathan H.,Brooks Carl A.,Carpenter Joseph,Probst Brandon L.,Jacobson Pamela,Glazier Seth W.,Ford Jes,Jensen James D.,Campbell Nicholas D.,Statnick Michael A.,Low Adeline S.,Thomas Kirk R.,Carpenter Anne E.,Hegde Sharath S.,Alfa Ronald W.,Victors Mason L.,Haque Imran S.,Chong Yolanda T.,Gibson Christopher C.
Abstract
ABSTRACTDevelopment of accurate disease models and discovery of immune-modulating drugs is challenged by the immune system’s highly interconnected and context-dependent nature. Here we apply deep-learning-driven analysis of cellular morphology to develop a scalable “phenomics” platform and demonstrate its ability to identify dose-dependent, high-dimensional relationships among and between immunomodulators, toxins, pathogens, genetic perturbations, and small and large molecules at scale. High-throughput screening on this platform demonstrates rapid identification and triage of hits for TGF-β- and TNF-α-driven phenotypes. We deploy the platform to develop phenotypic models of active SARS-CoV-2 infection and of COVID-19-associated cytokine storm, surfacing compounds with demonstrated clinical benefit and identifying several new candidates for drug repurposing. The presented library of images, deep learning features, and compound screening data from immune profiling and COVID-19 screens serves as a deep resource for immune biology and cellular-model drug discovery with immediate impact on the COVID-19 pandemic.
Publisher
Cold Spring Harbor Laboratory
Cited by
20 articles.
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