Evidence map›Paper›PMID 36901757›Full record

ArticleInternational journal of molecular sciences2023

TCF-1 Is Required for CD4 T Cell Persistence Functions during AlloImmunity.

Mahinbanu Mammadli, Liye Suo, Jyoti Misra Sen, Mobin Karimi

Open access · goldFull text read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. mInternational journal of oral science · 2024
    Article
  11. Article
  12. CD4Frontiers in immunology · 2023
    Article
  13. Review
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

4 authors at 2 institutions in 1 country.

Mahinbanu MammadliDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Liye SuoDepartment of Pathology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.ORCID 0000-0001-8838-5969
Jyoti Misra SenNational Institute on Aging-National Institute of Health, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Mobin KarimiDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.ORCID 0000-0002-3240-4814
SUNY Upstate Medical University · USJohns Hopkins University · US

Funding

T cell development in the thymus and age-dependent thymic involutionZIAAG000768 · NIA · NATIONAL INSTITUTE ON AGING · PI EGAN, JOSEPHINE · 2009 to 2025
$4.0M
Novel strategies to separate GVHD from GVTK22AI130182 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI KARIMI, MOBIN · 2017 to 2018
$266k
NIAID NIH HHS AI130182Upstate Medical University Cancer Center grant 1146249-1-75632
6 · The paper itself

Abstract

The transcription factor T cell factor-1 (TCF-1) is encoded by Tcf7 and plays a significant role in regulating immune responses to cancer and pathogens. TCF-1 plays a central role in CD4 T cell development; however, the biological function of TCF-1 on mature peripheral CD4 T cell-mediated alloimmunity is currently unknown. This report reveals that TCF-1 is critical for mature CD4 T cell stemness and their persistence functions. Our data show that mature CD4 T cells from TCF-1 cKO mice did not cause graft versus host disease (GvHD) during allogeneic CD4 T cell transplantation, and donor CD4 T cells did not cause GvHD damage to target organs. For the first time, we showed that TCF-1 regulates CD4 T cell stemness by regulating CD28 expression, which is required for CD4 stemness. Our data showed that TCF-1 regulates CD4 effector and central memory formation. For the first time, we provide evidence that TCF-1 differentially regulates key chemokine and cytokine receptors critical for CD4 T cell migration and inflammation during alloimmunity. Our transcriptomic data uncovered that TCF-1 regulates critical pathways during normal state and alloimmunity. Knowledge acquired from these discoveries will enable us to develop a target-specific approach for treating CD4 T cell-mediated diseases.

Indexed as

CD4-Positive T-LymphocytesGraft vs Host DiseaseAnimalsCD28 AntigensHepatocyte Nuclear Factor 1-alphaMiceMice, Inbred C57BLTranscription FactorsTransplantation, HomologousCD28 AntigensHepatocyte Nuclear Factor 1-alphaHnf1a protein, mouseTranscription FactorsalloimmunityCD4 T cell serum level cytokine productionCD4 T cells stemnessTCF-1

Identifiers

PMID36901757
PMCPMC10002223
OpenAlexW4321523293

What OpenQuestion holds

Textfull text, public
LicenceCC BY
reference markers read1
measurements read56
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 OpenQuestion graph.