KLF2 maintains lineage fidelity and suppresses CD8 T cell exhaustion during acute LCMV infection

Naïve CD8 T cells have the potential to differentiate into a spectrum of functional states during an immune response. How these developmental decisions are made and what mechanisms exist to suppress differentiation toward alternative fates remains unclear. We employed in vivo CRISPR-Cas9-based perturbation sequencing to assess the role of ~40 transcription factors (TFs) and epigenetic modulators in T cell fate decisions. Unexpectedly, we found that knockout of the TF <i>Klf2</i> resulted in aberrant differentiation to exhausted-like CD8 T cells during acute infection. KLF2 was required to suppress the exhaustion-promoting TF TOX and to enable the TF TBET to drive effector differentiation. KLF2 was also necessary to maintain a polyfunctional tumor-specific progenitor state. Thus, KLF2 provides effector CD8 T cell lineage fidelity and suppresses the exhaustion program.

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Publication Details

Journal
Science
Published
2025-02-13
DOI
https://doi.org/10.1126/science.adn2337
Citations
52
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
41.47
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article

KLF2 maintains lineage fidelity and suppresses CD8 T cell exhaustion during acute LCMV infection

Eric Fagerberg, Jaiveer Singh, Brian G. Hunt, Edward De Brouwer et al.
52 citations
Science
Immune Cell Function and Interaction
41.47
article

KLF2 maintains lineage fidelity and suppresses CD8 T cell exhaustion during acute LCMV infection

Eric Fagerberg, Jaiveer Singh, Brian G. Hunt, Edward De Brouwer, Weiguo Cui, Christine Dien, John S. Tsang, Smita Krishnaswamy, Leena Abdullah, Jian Shen, Nivedita R. Iyer, Kelli A. Connolly, Josephine R. Giles, Emily Kessler, Jessica N. Buck, John Attanasio, Martina Damo, Gena G. Foster, Yina H. Huang, Nikhil S. Joshi, Emily Borr, Jiaming He
article en
52 citations

Abstract

Naïve CD8 T cells have the potential to differentiate into a spectrum of functional states during an immune response. How these developmental decisions are made and what mechanisms exist to suppress differentiation toward alternative fates remains unclear. We employed in vivo CRISPR-Cas9-based perturbation sequencing to assess the role of ~40 transcription factors (TFs) and epigenetic modulators in T cell fate decisions. Unexpectedly, we found that knockout of the TF <i>Klf2</i> resulted in aberrant differentiation to exhausted-like CD8 T cells during acute infection. KLF2 was required to suppress the exhaustion-promoting TF TOX and to enable the TF TBET to drive effector differentiation. KLF2 was also necessary to maintain a polyfunctional tumor-specific progenitor state. Thus, KLF2 provides effector CD8 T cell lineage fidelity and suppresses the exhaustion program.

ScienceVol. 387(6735)
Dartmouth College (US), Northwestern University (US), Yale University (US), University of Chicago (US), Parker Institute for Cancer Immunotherapy (US), Chan Zuckerberg Initiative (United States) (US), Translational Therapeutics (United States) (US), University of Pennsylvania (US)
Good health and well-being
Openalex Percentile: Top 0%
Immune Cell Function and Interaction
41.47
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