Evidence map›Paper›PMID 36111104›Full record

ReviewFrontiers in medicine2022

COVID-19 and the potential of Janus family kinase (JAK) pathway inhibition: A novel treatment strategy.

Mansoor Khaledi, Fatemeh Sameni, Sheida Yahyazade, Maedeh Radandish, Parviz Owlia, Nader Bagheri, Hamed Afkhami, Mohamad Mahjoor, Zahra Esmaelpour, Maryam Kohansal and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Identification ofMolecules (Basel, Switzerland) · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. 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

11 authors at 6 institutions in 1 country.

Mansoor KhalediDepartment of Microbiology, Faculty of Medicine, Shahed University, Tehran, Iran.
Fatemeh SameniDepartment of Microbiology, Faculty of Medicine, Shahed University, Tehran, Iran.
Sheida YahyazadeDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Maedeh RadandishDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Parviz OwliaMolecular Microbiology Research Center, Faculty of Medicine, Shahed University, Tehran, Iran.
Nader BagheriCellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Hamed AfkhamiShahed University, Tehran, Iran.
Mohamad MahjoorDepartment of Immunology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Zahra EsmaelpourReference Laboratory for Bovine Tuberculosis, Razi Vaccine and Serum Research Institute, Karaj, Iran.
Maryam KohansalDepartment of Medical Biotechnology, Fasa University of Medical Sciences, Fasa, Iran.
Farzad AghaeiCellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Shahed University · IRIsfahan University of Medical Sciences · IRShahrekord University of Medical Sciences · IRFasa University of Medical Sciences · IRIran University of Medical Sciences · IRRazi Vaccine and Serum Research Institute · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidence proposed that the severity of the coronavirus disease 2019 (COVID-19) in patients is a consequence of cytokine storm, characterized by increased IL-1β, IL-6, IL-18, TNF-α, and IFN-γ. Hence, managing the cytokine storm by drugs has been suggested for the treatment of patients with severe COVID-19. Several of the proinflammatory cytokines involved in the pathogenesis of COVID-19 infection recruit a distinct intracellular signaling pathway mediated by JAKs. Consequently, JAK inhibitors, including baricitinib, pacritinib, ruxolitinib, and tofacitinib, may represent an effective therapeutic strategy for controlling the JAK to treat COVID-19. This study indicates the mechanism of cytokine storm and JAK/STAT pathway in COVID-19 as well as the medications used for JAK/STAT inhibitors.

Indexed as

baricitinibCOVID-19JAK inhibitorspacritinibruxolitinibtofacitinib

Identifiers

PMID36111104
PMCPMC9469902
OpenAlexW4293538014

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.