Evidence map›Paper›PMID 35459733›Full record

SynthesisJournal for immunotherapy of cancer2022

JAK inhibitors and COVID-19.

Gabriel Levy, Paola Guglielmelli, Peter Langmuir, Stefan N Constantinescu

Erratum issuedOpen access · goldAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
9.8field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 65 citations in OpenAlex.

  1. Pooled it
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  4. Dermatologic Toxicities Induced by JAK Inhibitors.American journal of clinical dermatology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 4 countries.

Gabriel LevySignal Transduction and Molecular Hematology, Ludwig Institute for Cancer Research, Brussels, Belgium.ORCID 0000-0001-6746-3083
Paola GuglielmelliDepartment of Clinical and Experimental Medicine, University of Florence, Firenze, Italy.
Peter LangmuirOncology Targeted Therapeutics, Incyte Corp, Wilmington, Delaware, USA.
Stefan N ConstantinescuSignal Transduction and Molecular Hematology, Ludwig Institute for Cancer Research, Brussels, Belgium stefan.constantinescu@uclouvain.be.ORCID 0000-0002-8599-2699
Ludwig Cancer Research · BEAzienda Ospedaliero-Universitaria Careggi · ITTarget (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During SARS-CoV-2 infection, the innate immune response can be inhibited or delayed, and the subsequent persistent viral replication can induce emergency signals that may culminate in a cytokine storm contributing to the severe evolution of COVID-19. Cytokines are key regulators of the immune response and virus clearance, and, as such, are linked to the-possibly altered-response to the SARS-CoV-2. They act via a family of more than 40 transmembrane receptors that are coupled to one or several of the 4 Janus kinases (JAKs) coded by the human genome, namely JAK1, JAK2, JAK3, and TYK2. Once activated, JAKs act on pathways for either survival, proliferation, differentiation, immune regulation or, in the case of type I interferons, antiviral and antiproliferative effects. Studies of graft-versus-host and systemic rheumatic diseases indicated that JAK inhibitors (JAKi) exert immunosuppressive effects that are non-redundant with those of corticotherapy. Therefore, they hold the potential to cut-off pathological reactions in COVID-19. Significant clinical experience already exists with several JAKi in COVID-19, such as baricitinib, ruxolitinib, tofacitinib, and nezulcitinib, which were suggested by a meta-analysis (Patoulias

Indexed as

COVID-19 Drug TreatmentJanus Kinase InhibitorsAntiviral AgentsAzetidinesCytokinesHumansImidazolesIndazolesPiperidinesSARS-CoV-2Antiviral AgentsAzetidinesCytokinesImidazolesIndazolesJanus Kinase InhibitorsnezulcitinibPiperidinesautoimmunityCOVID-19cytokineshematologic neoplasmstherapies, investigational

Identifiers

PMID35459733
PMCPMC9035837
OpenAlexW4224314146

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.