Multimodal stimulation screens reveal unique and shared genes limiting T cell fitness

Chun Pu Lin, Pierre L. Levy, Astrid Alflen, Georgi Apriamashvili, Maarten A. Ligtenberg, David W. Vredevoogd, Onno B. Bleijerveld, Ferhat Alkan, Yuval Malka, Liesbeth Hoekman, Ettai Markovits, Austin George, Joleen J.H. Traets, Oscar Krijgsman, Alex van Vliet, Joanna Poźniak, Carlos Ariel Pulido-Vicuña, Beaunelle de Bruijn, Susan E. van Hal-van Veen, Julia BoshuizenPim W. van der Helm, Judit Díaz-Gómez, Hamdy Warda, Leonie M. Behrens, Paula Mardesic, Bilal Dehni, Nils L. Visser, Jean Christophe Marine, Gal Markel, William J. Faller, Maarten Altelaar, Reuven Agami, Michal J. Besser, Daniel S. Peeper*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Genes limiting T cell antitumor activity may serve as therapeutic targets. It has not been systematically studied whether there are regulators that uniquely or broadly contribute to T cell fitness. We perform genome-scale CRISPR-Cas9 knockout screens in primary CD8 T cells to uncover genes negatively impacting fitness upon three modes of stimulation: (1) intense, triggering activation-induced cell death (AICD); (2) acute, triggering expansion; (3) chronic, causing dysfunction. Besides established regulators, we uncover genes controlling T cell fitness either specifically or commonly upon differential stimulation. Dap5 ablation, ranking highly in all three screens, increases translation while enhancing tumor killing. Loss of Icam1-mediated homotypic T cell clustering amplifies cell expansion and effector functions after both acute and intense stimulation. Lastly, Ctbp1 inactivation induces functional T cell persistence exclusively upon chronic stimulation. Our results functionally annotate fitness regulators based on their unique or shared contribution to traits limiting T cell antitumor activity.

Original languageEnglish
Article numbere10
Pages (from-to)623-645
Number of pages23
JournalCancer Cell
Volume42
Issue number4
DOIs
Publication statusPublished - 8 Apr 2024

Bibliographical note

Publisher Copyright:
© 2024 The Authors

Keywords

  • activation-induced cell death
  • cancer immunotherapy
  • CRISPR-Cas9 screen
  • Ctbp1
  • Dap5
  • dysfunction
  • effector function
  • exhaustion
  • Icam1
  • T cells

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