Evidence map›Paper›PMID 31375130›Full record

ArticleArthritis research & therapy2019

Comparison of baricitinib, upadacitinib, and tofacitinib mediated regulation of cytokine signaling in human leukocyte subpopulations.

Iain B McInnes, Nicole L Byers, Richard E Higgs, Jonathan Lee, William L Macias, Songqing Na, Robert A Ortmann, Guilherme Rocha, Terence P Rooney, Thomas Wehrman and 3 more

Registry-linked trialOpen access · goldAbstract readComparative Study
In one paragraph

Article in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04332042 (TOFAcitinib in Patients With Early Onset SARS-CoV2 Interstitial Pneumonia), which is not on this map. Cited by 158 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
158citing papers in PubMed, 3 pooled it
13.0field-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.

NCT04332042 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

TOFAcitinib in Patients With Early Onset SARS-CoV2 Interstitial Pneumonia

TypeinterventionalSponsorUniversità Politecnica delle MarcheRan2020 to 2020Enrolled50ConditionsSARS-COv2 Related Interstitial PneumoniaArmsTofacitinib
3 · Its place in the literature

Who cites it

158 citing papers in PubMed, 3 syntheses or guidelines pooled it, 278 citations in OpenAlex.

  1. JAK inhibitors and COVID-19.Journal for immunotherapy of cancer · 2022
    Pooled it
  2. Pooled it
  3. Guideline
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Article
  9. JAK inhibitors and menstrual cycle alterations: insights from a case series of 16 female patients.Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG · 2026
    Article
  10. Article
  11. Article
  12. Pharmacologic Inhibition of JAK1/2 Potentiates Aminoglycoside-Induced Ototoxicity.Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2026
    Article
  13. Myopathies in clinical care: a focus on treatable causes.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Crohn's disease exacerbated by ghost pills of upadacitinib.Clinical journal of gastroenterology · 2025
    Article
  19. Article
  20. Article

98 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

13 authors at 4 institutions in 2 countries.

Iain B McInnesInstitute of Infection, Immunity and Inflammation, University of Glasgow, University Avenue, Glasgow, G128QQ, UK. Iain.McInnes@glasgow.ac.uk.
Nicole L ByersEli Lilly and Company, Indianapolis, IN, USA.
Richard E HiggsEli Lilly and Company, Indianapolis, IN, USA.
Jonathan LeeEli Lilly and Company, Indianapolis, IN, USA.
William L MaciasEli Lilly and Company, Indianapolis, IN, USA.
Songqing NaEli Lilly and Company, Indianapolis, IN, USA.
Robert A OrtmannEli Lilly and Company, Indianapolis, IN, USA.
Guilherme RochaEli Lilly and Company, Indianapolis, IN, USA.
Terence P RooneyEli Lilly and Company, Indianapolis, IN, USA.
Thomas WehrmanPrimity Bio, Fremont, CA, USA.
Xin ZhangEli Lilly and Company, Indianapolis, IN, USA.
Steven H ZuckermanEli Lilly and Company, Indianapolis, IN, USA.
Peter C TaylorBotnar Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
Eli Lilly (United States) · USPrimity Bio (United States) · USUniversity of Glasgow · GBUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe in vitro pharmacology of baricitinib, upadacitinib, and tofacitinib was evaluated to understand differences among these JAK inhibitors (JAKis) at the cellular level.

methodsPeripheral blood mononuclear cells from healthy donors were incubated with different JAKis, levels of phosphorylated signal transducer and activator of transcription (pSTAT) were measured following cytokine stimulation, and half maximum inhibitory concentration (IC

resultsDistinct JAKis displayed different in vitro pharmacologic profiles. For example, tofacitinib and upadacitinib were the most potent inhibitors of the JAK1/3-dependent cytokines tested (interleukin [IL]-2, IL-4, IL-15, and IL-21) with lower IC

conclusionsDifferent JAKis modulated distinct cytokine pathways to varying degrees, and no agent potently or continuously inhibited an individual cytokine signaling pathway throughout the dosing interval. Notably, baricitinib inhibited JAK1/3 signaling to a lesser extent than upadacitinib and tofacitinib, while upadacitinib, baricitinib, and tofacitinib inhibited the signaling of JAK2/2-dependent cytokines, including GM-CSF and IL-3, as well as the signaling of the JAK2/TYK2-dependent cytokine G-CSF.

Indexed as

Arthritis, RheumatoidAzetidinesBiomarkersCytokinesFlow CytometryHeterocyclic Compounds, 3-RingHumansJanus Kinase InhibitorsLeukocytes, MononuclearPiperidinesProtein Kinase InhibitorsPurinesPyrazolesPyrimidinesPyrrolesSignal TransductionAzetidinesbaricitinibBiomarkersCytokinesHeterocyclic Compounds, 3-RingJanus Kinase InhibitorsPiperidinesProtein Kinase InhibitorsPurinesPyrazolesPyrimidinesPyrrolesSulfonamidestofacitinibupadacitinibBaricitinibCytokineJanus kinasePhosphorylated signal transducer and activator of transcriptionPotencyReceptor kinase signalingRheumatoid arthritisSelectivityTofacitinibUpadacitinib

Identifiers

PMID31375130
PMCPMC6679539
OpenAlexW2966093740

What OpenQuestion holds

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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.