Evidence map›Paper›PMID 34847076›Full record

ArticleJCI insight2022

Pirfenidone increases IL-10 and improves acute pancreatitis in multiple clinically relevant murine models.

Ejas Palathingal Bava, John George, Mohammad Tarique, Srikanth Iyer, Preeti Sahay, Beatriz Gomez Aguilar, Dujon B Edwards, Bhuwan Giri, Vrishketan Sethi, Tejeshwar Jain and 8 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05350371 (Evaluation of Pirfenidone as a Therapy in Patients With Predicted Moderate to Severe Acute Pancreatitis), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.0field-weighted citation impact, top 4% 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.

NCT05350371 phase1 / phase2recruitingnot on this mapstarted 2023, after this paper: background citation

Evaluation of Pirfenidone as a Therapy in Patients With Predicted Moderate to Severe Acute Pancreatitis

TypeinterventionalSponsorUniversity of Alabama at BirminghamRan2023 to 2027Enrolled60ConditionsPancreatitis, AcuteArmsPirfenidone Oral Tablet, Placebo
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Genetic and pharmacologic modulations elucidate NRF2 protective role in acute pancreatitis.American journal of physiology. Gastrointestinal and liver physiology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Acute pancreatitis: mechanisms and therapeutic approaches.Signal transduction and targeted therapy · 2026
    Review
  8. Article
  9. L-arginine-induced chronic pancreatitis in mice: Evaluating effects of pirfenidone and simvastatin.World journal of gastrointestinal pharmacology and therapeutics · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Renalase peptides reduce pancreatitis severity in mice.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  16. Pirfenidone use in fibrotic diseases: What do we know so far?Immunity, inflammation and disease · 2024
    Review
  17. Article
  18. Interleukins: pathophysiological role in acute pancreatitis.Archives of medical science : AMS · 2024
    Article
  19. Article
  20. Observational
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

18 authors at 2 institutions in 1 country.

Ejas Palathingal BavaDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
John GeorgeDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Mohammad TariqueDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Srikanth IyerDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Preeti SahayDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Beatriz Gomez AguilarDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Dujon B EdwardsDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Bhuwan GiriDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Vrishketan SethiDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Tejeshwar JainDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Prateek SharmaDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Utpreksha VaishDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Harrys K C JacobDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Anthony FerrantellaDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Craig L MaynardDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Ashok K SalujaDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Rajinder K DawraDepartment of Surgery and Sylvester Comprehensive Cancer Center, University of Miami, Miami, Florida, USA.
Vikas DudejaDepartment of Surgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Sylvester Comprehensive Cancer Center · USUniversity of Alabama at Birmingham · US

Funding

Therapeutic efficacy of Pirfenidone in PancreatitisR01DK111834 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI DUDEJA, VIKAS · 2017 to 2020
$1.4M
NIDDK NIH HHS R01 DK111834
6 · The paper itself

Abstract

Despite decades of research, there is no specific therapy for acute pancreatitis (AP). In the current study, we have evaluated the efficacy of pirfenidone, an antiinflammatory and antifibrotic agent that is approved by the FDA for treatment of idiopathic pulmonary fibrosis (IPF), in ameliorating local and systemic injury in AP. Our results suggest that treatment with pirfenidone in therapeutic settings (e.g., after initiation of injury), even when administered at the peak of injury, reduces severity of local and systemic injury and inflammation in multiple models of AP. In vitro evaluation suggests that pirfenidone decreases cytokine release from acini and macrophages and disrupts acinar-macrophage crosstalk. Therapeutic pirfenidone treatment increases IL-10 secretion from macrophages preceding changes in histology and modulates the immune phenotype of inflammatory cells with decreased levels of inflammatory cytokines. Antibody-mediated IL-10 depletion, use of IL-10-KO mice, and macrophage depletion experiments confirmed the role of IL-10 and macrophages in its mechanism of action, as pirfenidone was unable to reduce severity of AP in these scenarios. Since pirfenidone is FDA approved for IPF, a trial evaluating the efficacy of pirfenidone in patients with moderate to severe AP can be initiated expeditiously.

Indexed as

FibrosisPancreasPancreatitisAcinar CellsAnimalsAnti-Inflammatory Agents, Non-SteroidalCells, CulturedCytokinesDisease Models, AnimalInterleukin-10MacrophagesMiceParacrine CommunicationPyridonesSignal TransductionAnti-Inflammatory Agents, Non-SteroidalCytokinesIL10 protein, mouseInterleukin-10pirfenidonePyridonesChemokinesCytokinesGastroenterologyInflammationMacrophages

Identifiers

PMID34847076
PMCPMC8855813
OpenAlexW3217556469

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.