Evidence map›Paper›PMID 34777255›Full record

ReviewFrontiers in endocrinology2021

Emerging Roles of T Cells in the Pathogenesis of Nonalcoholic Steatohepatitis and Hepatocellular Carcinoma.

Petra Hirsova, Adebowale O Bamidele, Haiguang Wang, Davide Povero, Xavier S Revelo

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
7.7field-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

48 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. From model to man: Understanding Tregs' dual role in MASLD.JHEP reports : innovation in hepatology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Do autoantigens drive MASH progression?Hepatology (Baltimore, Md.) · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. The Role of CD4International journal of molecular sciences · 2024
    Review
  17. Review
  18. Review
  19. The PD-1/PD-L1 Axis in the Biology of MASLD.International journal of molecular sciences · 2024
    Review
  20. 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

5 authors at 2 institutions in 1 country.

Petra HirsovaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Adebowale O BamideleDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, United States.
Haiguang WangDepartment of Integrative Biology and Physiology, University of Minnesota, Minneapolis, MN, United States.
Davide PoveroDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, United States.
Xavier S ReveloDepartment of Integrative Biology and Physiology, University of Minnesota, Minneapolis, MN, United States.
Mayo Clinic in Arizona · USUniversity of Minnesota · US

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
DIABETES AND METABOLISMT32DK007352 · NIDDK · MAYO CLINIC ROCHESTER · PI MICHAEL D. JENSEN · 1986 to 2026
$9.4M
Immune Mechanisms Regulating Cardiac RemodelingR01HL155993 · NHLBI · UNIVERSITY OF MINNESOTA · PI REVELO, XAVIER, VAN BERLO, JOHANNES (JOP) · 2021 to 2024
$2.9M
Pathobiology of Nonalcoholic SteatohepatitisR01DK130884 · NIDDK · MAYO CLINIC ROCHESTER · PI Petra Hirsova · 2021 to 2026
$2.5M
Mechanisms of B Cell Pathogenicity in Non-Alcoholic Fatty Liver DiseaseR01DK122056 · NIDDK · UNIVERSITY OF MINNESOTA · PI REVELO, XAVIER · 2019 to 2023
$1.7M
Gastrointestinal Cues Influence Metabolic Control of Regulatory T cell FunctionK01DK124358 · NIDDK · MAYO CLINIC ROCHESTER · PI BAMIDELE, ADEBOWALE O · 2020 to 2024
$723k
NHLBI NIH HHS R01 HL155993NIDDK NIH HHS K01 DK124358NIDDK NIH HHS P30 DK084567NIDDK NIH HHS R01 DK122056NIDDK NIH HHS R01 DK130884NIDDK NIH HHS T32 DK007352
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) has become the most common chronic liver disease worldwide. A significant proportion of patients with NAFLD develop a progressive inflammatory condition termed nonalcoholic steatohepatitis (NASH), which may eventually advance to cirrhosis and hepatocellular carcinoma (HCC). NASH is characterized by steatosis, hepatocyte ballooning, and lobular inflammation. Heightened immune cell infiltration is a hallmark of NASH, yet the mechanisms whereby hepatic inflammation occurs in NASH and how it contributes to disease initiation and progression remain incompletely understood. Emerging evidence indicates that intrahepatic T cell immune mechanisms play an integral role in the pathogenesis of NASH and its transition to HCC. In this review, we summarize the current knowledge regarding the T cell-mediated mechanisms of inflammation in NASH. We highlight recent preclinical and human studies implicating various subsets of conventional and innate-like T cells in the onset and progression of NASH and HCC. Finally, we discuss the potential therapeutic strategies targeting T cell-mediated responses for the treatment of NASH.

Indexed as

AnimalsCarcinoma, HepatocellularHumansInflammationLiver CirrhosisLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseT-LymphocytesCD4/CD8 lymphocytesHCCInflammationNASHT cells

Identifiers

PMID34777255
PMCPMC8581300
OpenAlexW3210485981

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.