Evidence map›Paper›PMID 29915024›Full record

ArticleThe Journal of experimental medicine2018

Effector CD4 T cells with progenitor potential mediate chronic intestinal inflammation.

Boyoung Shin, Robert L Kress, Philip A Kramer, Victor M Darley-Usmar, Susan L Bellis, Laurie E Harrington

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Progenitor exhausted PD-1Nature cardiovascular research · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Erlotinib suppresses tumorigenesis in a mouse model of colitis-associated cancer.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2024
    Article
  13. Durable CD4Trends in immunology · 2024
    Review
  14. Review
  15. Immunometabolism (Cobham, Surrey) · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Sweet Immune Checkpoint Targets to Enhance T Cell Therapy.Journal of immunology (Baltimore, Md. : 1950) · 2022
    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

6 authors.

Boyoung ShinDepartment of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-7926-5527
Robert L KressDepartment of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL.
Philip A KramerDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL.
Victor M Darley-UsmarDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL.
Susan L BellisDepartment of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL.
Laurie E HarringtonDepartment of Cell, Developmental, and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL lharring@uab.edu.ORCID 0000-0002-6832-9529

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
UAB-UCSD O'Brien Core Center for Acute Kidney Injury ResearchP30DK079337 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AGARWAL, ANUPAM · 2008 to 2022
$18.3M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
STAT4 regulation of effector CD4 T cells and CNS inflammationR01AI113007 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HARRINGTON, LAURIE ELLEN · 2015 to 2019
$1.8M
Regulation of effector CD4 T cell subsets during inflammatory bowel diseaseR01DK084082 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HARRINGTON, LAURIE ELLEN · 2010 to 2014
$1.6M
Glycosylation-dependent mechanisms regulating ovarian tumor cell survivalR01GM111093 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BELLIS, SUSAN L · 2014 to 2017
$874k
NCI NIH HHS P30 CA013148NIAID NIH HHS R01 AI113007NIAMS NIH HHS P30 AR048311NIDDK NIH HHS P30 DK079337NIDDK NIH HHS R01 DK084082NIGMS NIH HHS R01 GM111093
6 · The paper itself

Abstract

Dysregulated CD4 T cell responses are causally linked to autoimmune and chronic inflammatory disorders, yet the cellular attributes responsible for maintaining the disease remain poorly understood. Herein, we identify a discrete population of effector CD4 T cells that is able to both sustain and confer intestinal inflammation. This subset of pathogenic CD4 T cells possesses a unique gene signature consistent with self-renewing T cells and hematopoietic progenitor cells, exhibits enhanced survival, and continually seeds the terminally differentiated IFNγ-producing cells in the inflamed intestine. Mechanistically, this population selectively expresses the glycosyltransferase ST6Gal-I, which is required for optimal expression of the stemness-associated molecule TCF1 by effector CD4 T cells. Our findings indicate that the chronicity of T cell-mediated inflammation is perpetuated by specific effector CD4 T cells with stem-like properties.

Indexed as

Animalsbeta-D-Galactoside alpha 2-6-SialyltransferaseCD4-Positive T-LymphocytesCell DifferentiationCell Self RenewalCell SurvivalChronic DiseaseColitisGene Expression ProfilingHepatocyte Nuclear Factor 1-alphaInflammationInterferon-gammaIntestinesMice, Inbred C57BLMitochondriaN-Acetylneuraminic Acidbeta-D-Galactoside alpha 2-6-SialyltransferaseHepatocyte Nuclear Factor 1-alphaHnf1a protein, mouseInterferon-gammaN-Acetylneuraminic AcidSialyltransferases

Identifiers

PMID29915024
PMCPMC6028516

What OpenQuestion holds

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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.