Evidence map›Paper›PMID 34635393›Full record

ReviewTrends in immunology2021

RORγt protein modifications and IL-17-mediated inflammation.

Ritesh Kumar, Arianne L Theiss, K Venuprasad

Open access · greenAbstract readReview
In one paragraph

Review in Trends in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 2% 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

100 citing papers in PubMed, 1 synthesis or guideline pooled it, 150 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Article
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  15. The Role of CD4Cells · 2026
    Review
  16. Article
  17. Frontiers in microbiology · 2026
    Article
  18. Review
  19. Review
  20. mFrontiers in immunology · 2026
    Review

40 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 1 country.

Ritesh KumarDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX 75390, USA; Department of Immunology, UT Southwestern Medical Center, Dallas, TX 75390, USA; Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Arianne L TheissUniversity of Colorado, School of Medicine, Division of Gastroenterology and Hepatology, Anschutz Medical Campus, Aurora, CO 80045, USA.
K VenuprasadDepartment of Internal Medicine, UT Southwestern Medical Center, Dallas, TX 75390, USA; Department of Immunology, UT Southwestern Medical Center, Dallas, TX 75390, USA; Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: Venuprasad.poojary@utsouthwestern.edu.
Southwestern Medical CenterSouthwestern Medical Center · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Regulation of CD8+T cells by Zbtb42R01CA266072 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI Venuprasad K Poojary · 2022 to 2026
$2.1M
Regulation of Zbtb44-Eomes complex in CD8+T cells and anti-tumor immunityR01AI155786 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI POOJARY, VENUPRASAD K · 2021 to 2025
$2.1M
Mitochondrial Dysfunction and Mitophagy in IleitisR01DK117001 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI THEISS, ARIANNE L · 2018 to 2022
$1.9M
Regulation of ROR-gt in colonic inflammationR01DK115668 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI POOJARY, VENUPRASAD K · 2018 to 2021
$1.5M
NCI NIH HHS R01 CA266072NIAID NIH HHS R01 AI155786NIDDK NIH HHS R01 DK115668NIDDK NIH HHS R01 DK117001
6 · The paper itself

Abstract

RORγt, the master transcription factor for cytokine interleukin (IL)-17, is expressed explicitly in Th17 cells, γδT cells, and type 3 innate lymphoid cells in mice and humans. Since dysregulated IL-17 expression is strongly linked to several human inflammatory diseases, the RORγt-IL-17 axis has been the focus of intense research. Recently, several studies have shown that RORγt is modified by multiple post-translational mechanisms, including ubiquitination, acetylation, SUMOylation, and phosphorylation. This review discusses how post-translational modifications modulate RORγt function and its turnover to regulate IL-17-driven inflammation. Broad knowledge of these pathways is crucial for a clear understanding of the pathogenic role of RORγt

Indexed as

Interleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3AnimalsCell DifferentiationHumansImmunity, InnateInflammationMiceProtein Processing, Post-TranslationalTh17 CellsInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3autoimmune diseasesIL-17post-translational modificationsRORγtTh17

Identifiers

PMID34635393
PMCPMC8556362
OpenAlexW3207817598

What OpenQuestion 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 OpenQuestion graph.