Evidence map›Paper›PMID 38301652›Full record

ArticleImmunity2024

Reversible, tunable epigenetic silencing of TCF1 generates flexibility in the T cell memory decision.

Kathleen Abadie, Elisa C Clark, Rajesh M Valanparambil, Obinna Ukogu, Wei Yang, Riza M Daza, Kenneth K H Ng, Jumana Fathima, Allan L Wang, Judong Lee and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
10.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
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  8. Design principles of the cytotoxic CD8Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Review
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  11. Article
  12. Regulators of CD8Nature reviews. Immunology · 2026
    Review
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  15. Article
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  17. Article
  18. Design principles of the cytotoxic CD8bioRxiv : the preprint server for biology · 2025
    Article
  19. Article
  20. Pre-division TCF1 drop determines long-term CD8 T cell fates.bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 1 country.

Kathleen AbadieDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Elisa C ClarkDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Rajesh M ValanparambilEmory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Obinna UkoguDepartment of Applied Mathematics, University of Washington, Seattle, WA 98105, USA.
Wei YangDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Riza M DazaDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Kenneth K H NgDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Jumana FathimaDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Allan L WangDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Judong LeeEmory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Tahseen H NastiEmory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Avinash BhandoolaT-Cell Biology and Development Unit, Laboratory of Genome Integrity, Center for Cancer Research, National Cancer Institute, National Institute of Health, Bethesda, MD 20892, USA.
Armita NourmohammadDepartment of Applied Mathematics, University of Washington, Seattle, WA 98105, USA; Department of Physics, University of Washington, Seattle, WA 98105, USA; Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Rafi AhmedEmory Vaccine Center and Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA; Brotman Baty Institute for Precision Medicine, Seattle, WA 98195, USA; Allen Discovery Center for Cell Lineage Tracing, Seattle, WA 98109, USA; Howard Hughes Medical Institute, Seattle, WA 98195, USA; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA. Electronic address: shendure@uw.edu.
Junyue CaoDepartment of Genome Sciences, University of Washington, Seattle, WA 98195, USA; Laboratory of Single-Cell Genomics and Population Dynamics, The Rockefeller University, New York, NY 10065, USA. Electronic address: jcao@rockefeller.edu.
Hao Yuan KuehDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA. Electronic address: kueh@uw.edu.
University of Washington · USEmory University · USHoward Hughes Medical Institute · USNational Cancer Institute · USUniversity of Washington Applied Physics Laboratory · US

Funding

T cell Development and RegenerationZIABC011633 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BHANDOOLA, AVINASH · 2015 to 2025
$20.5M
Versatile, exponentially scalable methods for single cell molecular profilingR01HG010632 · NHGRI · UNIVERSITY OF WASHINGTON · PI Jay Ashok Shendure, Bruce Colston Trapnell · 2019 to 2026
$5.9M
T CELL MEMORY TO VIRUSESR01AI030048 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AHMED, RAFI · 1990 to 2022
$5.2M
Learning a molecular shape space for the adaptive immune systemR35GM142795 · NIGMS · UNIVERSITY OF WASHINGTON · PI NOURMOHAMMAD, ARMITA · 2021 to 2025
$1.8M
Input encoding in T-cell receptor signalingR21EB027327 · NIBIB · UNIVERSITY OF WASHINGTON · PI KUEH, HAO YUAN · 2019 to 2021
$622k
NHGRI NIH HHS R01 HG010632NIAID NIH HHS R01 AI030048NIBIB NIH HHS R21 EB027327NIGMS NIH HHS R35 GM142795
6 · The paper itself

Abstract

The immune system encodes information about the severity of a pathogenic threat in the quantity and type of memory cells it forms. This encoding emerges from lymphocyte decisions to maintain or lose self-renewal and memory potential during a challenge. By tracking CD8

Indexed as

CD8-Positive T-LymphocytesMemory T CellsCell DifferentiationClone CellsEpigenesis, GeneticImmunologic Memoryacute infectioncell fate decisionsimmune memorylineage plasticitylive-cell imagingmathematical modelingsingle-cell dynamicssystems immunologyT cell differentiationtime-resolved single-cell RNA-seq

Identifiers

PMID38301652
PMCPMC10922671
OpenAlexW4391406674

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.