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April 5, 2026Cancer Research0 citations

Abstract 4258: In vivo genome-scale enhancer screen decodes T cell fate decisions in the tumor

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KJKeely JiACAlex Chang-Yu ChenLHLaura G. Hinojosa

Key Points

  • This research aims to identify the regulatory elements within the core exhaustion program that drive T cell dysfunction during cancer.
  • Utilized a pooled CRISPR-based enhancer deletion platform (SNIP-R) for kilobase-scale perturbations in primary T cells.
  • Conducted an in vivo genome-scale enhancer deletion screen on OVA-specific CD8+ T cells in OVA-expressing tumors.
  • Identified regulatory networks within the core exhaustion program affecting T cell persistence and differentiation.
  • Discovered a regulatory element located 100kb upstream of the Klf6 gene that improves tumor control when deleted.
  • Klf6-100kb perturbed T cells showed increased competition against control populations and higher generation of effector-like T cells.
  • Established that the core exhaustion program contains causal regulatory elements behind T cell exhaustion.

Abstract

Abstract During chronic infection and cancer progression, T cells enter a dysfunctional state called exhaustion, posing a significant challenge to disease control and immunotherapy outcomes. Previously, we and others have shown that T cell exhaustion is a differentiation process regulated at the epigenetic level. Exhausted T cells share a conserved program of chromatin accessibility landscapes across chronic infections and tumors (core exhaustion program) that is imprinted in early T cell differentiation. However, it remains unclear whether and which open chromatin regions within the core exhaustion program play a causal role in driving the exhausted state. We hypothesize that the core exhaustion program contains transcriptional enhancers that regulate T cell persistence and differentiation in exhaustion, preventing reinvigoration of function. To test it, we leveraged our novel enhancer editing platform called Systematic Non-coding element Interrogation by Paired sgRNAs (SNIP-R), a pooled CRISPR-based enhancer deletion platform optimized for kilobase-scale perturbation in primary T cells. We performed the first in vivo genome-scale enhancer deletion screen on ova-specific CD8+ T cells (OT-1) in OVA-expressing tumors. We identified networks of regulatory elements in the core exhaustion program that regulate T cell persistence and subset formation in the tumor. Validation studies from the screen showed that deleting one such regulatory element 100kb upstream of the Klf6 gene (Klf6-100kb) in T cells improved tumor control. Klf6-100kb perturbed T cells strongly outcompeted control populations and had increased generation of effector-like T cells in the tumor compared to control perturbations. Together, we showed that the core exhaustion program contains causal regulatory elements underlying T cell exhaustion and pinpointed new targets for developing next-generation adoptive T cell therapies. Citation Format: Keely Y. Ji, Alex Chang-Yu Chen, Laura Hinojosa, Bolutito Babatunde, Daniela Martinez, Thomas J. LaSalle, Maria Zschummel, Marc A. Schwartz, Ferhat Ay, Debattama Sen. In vivo genome-scale enhancer screen decodes T cell fate decisions in the tumor abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4258.

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Cite This Study

Ji et al. (2026) studied this question.

synapsesocial.com/papers/69d1fcd4a79560c99a0a2928https://doi.org/10.1158/1538-7445.am2026-4258
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Abstract 7042: Enhancing TCR T cell function in solid tumors through in vivo combinatorial screens and single-cell analysis2024
  2. 2Abstract 7034: Pooled CRISPR screening coupled with single-cell sequencing identifies modifiers of CAR T cell state in the context of chronic antigen stimulation2024
  3. 3Abstract 5625: Epigenetic reprogramming of T cell exhaustion2026
  4. 4Abstract 1689: CRISPR functional genetic screening for immune enhancers of inhibitor receptors in human primary CD8 T cells2024
  5. 5Abstract LT02: Regulation of Exhausted CD8+ T cell Differentiation by IKZF Transcription Factors2024 · 1 citations