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Microfluidics guided by deep learning for cancer immunotherapy screening.
Ao, Zheng; Cai, Hongwei; Wu, Zhuhao; Hu, Liya; Nunez, Asael; Zhou, Zhuolong; Liu, Hongcheng; Bondesson, Maria; Lu, Xiongbin; Lu, Xin; Dao, Ming; Guo, Feng.
Affiliation
  • Ao Z; Department of Intelligent Systems Engineering, Indiana University, Bloomington, IN 47405.
  • Cai H; Department of Intelligent Systems Engineering, Indiana University, Bloomington, IN 47405.
  • Wu Z; Department of Intelligent Systems Engineering, Indiana University, Bloomington, IN 47405.
  • Hu L; Department of Intelligent Systems Engineering, Indiana University, Bloomington, IN 47405.
  • Nunez A; Department of Intelligent Systems Engineering, Indiana University, Bloomington, IN 47405.
  • Zhou Z; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Liu H; Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Bondesson M; Department of Industrial and Systems Engineering, University of Florida, Gainesville, FL 32611.
  • Lu X; Department of Intelligent Systems Engineering, Indiana University, Bloomington, IN 47405.
  • Lu X; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Dao M; Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN 46202.
  • Guo F; Melvin and Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, IN 46202.
Proc Natl Acad Sci U S A ; 119(46): e2214569119, 2022 11 16.
Article in En | MEDLINE | ID: mdl-36343225
ABSTRACT
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Deep Learning / Neoplasms Type of study: Diagnostic_studies / Screening_studies Limits: Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Deep Learning / Neoplasms Type of study: Diagnostic_studies / Screening_studies Limits: Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2022 Type: Article