Evidence map›Paper›PMID 42187316›Full record

SynthesisJournal of the European Academy of Dermatology and Venereology : JEADV2026

Large-scale meta-analysis of infection risk with JAK-STAT inhibitors in 29,000 patients.

Máté Krebs, Lili Gulyás, Karen Krisztina Fazekas, Benedek Nagy, Mária Veronika Kolonics, Fanni Adél Meznerics, Norbert Kiss, András Bánvölgyi, Péter Hegyi, Péter Holló and 1 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Journal of the European Academy of Dermatology and Venereology : JEADV, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Large-scale meta-analysis of infection risk with JAK-STAT inhibitors in 29,000 patients.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Pooled it
  2. 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.

Máté KrebsDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0009-0004-6394-4276
Lili GulyásDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Karen Krisztina FazekasCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Benedek NagyDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Mária Veronika KolonicsDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Fanni Adél MeznericsDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Norbert KissDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
András BánvölgyiDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Péter HegyiCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Péter HollóDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Lajos Vince KeményDepartment of Dermatology, Venereology and Dermatooncology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionJanus kinase signal transducer and transcription activator (JAK-STAT) inhibitors have revolutionized the treatment of immune-mediated inflammatory diseases (IMIDs) of the skin, such as in atopic dermatitis, alopecia areata and vitiligo. Although several meta-analyses have confirmed their efficacy, concerns remain about the risk of infection, as the JAK-STAT pathway plays a key role in immune defence. Previous meta-analyses examined only selected, pre-specified infection categories and have not comprehensively evaluated all reported infection types or compared systemic and topical agents.

methodsWe performed a systematic review and meta-analysis of randomized controlled trials (RCTs) that reported infection-related adverse events in patients treated with systemic or topical JAK-STAT inhibitors for IMIDs of the skin. The study followed the PRISMA 2020 and Cochrane guidelines (PROSPERO: CRD 42024615839). Overall risk ratios (RRs) with 95% confidence intervals (CI) were calculated using a random-effects model.

resultsSeventy-four RCTs were included, involving more than 29,000 patients. JAK-STAT inhibitors were associated with an increased risk of influenza (RR = 2.12, 95% CI 1.03-4.36), bronchitis (RR = 2.03, 95% CI 1.43-2.88) and herpes zoster (RR = 1.67, 95% CI 1.29-2.15) compared to a placebo. The risk was particularly elevated in patients with atopic dermatitis (influenza: 3.22, 95% CI 2.03-5.10, herpes zoster: RR = 2.00, 95% CI 1.34-2.99). No significant risks were identified for serious, fungal or opportunistic infections, and topical JAK-STAT inhibitors demonstrated a favourable safety profile comparable to vehicle controls.

conclusionsThis meta-analysis provides a comprehensive assessment of the risk of infection associated with JAK-STAT inhibitors in IMIDs of the skin. Although overall safety is acceptable, clinicians should be aware of the higher infection risk of influenza and herpes zoster and should consider vaccination and preventive strategies for high-risk patients with atopic dermatitis. The main limitation is that the included studies involved highly selected populations with few comorbidities and short follow-up.

Indexed as

Janus Kinase InhibitorsJanus KinasesSTAT Transcription FactorsHumansRandomized Controlled Trials as TopicJanus Kinase InhibitorsJanus KinasesSTAT Transcription Factorsabrocitinibadverse reactionsatopic dermatitisbaricitinibbrepocitinibdelgocitinibdeucravacitinibdeuruxolitinibfilgotinibgusacitinibherpes zosterimmune‐mediated inflammatory diseases of the skininfection riskinfluenzaitacitinibivarmacitinibJAK–STAT inhibitorJanus kinase inhibitorspeficitinibpovorcitinibritlecitinibropsacitinibruxolitinibtofacitinibupadacitinibzasocitinib

Identifiers

PMID42187316
PMCPMC13613348

What OpenQuestion holds

Textmetadata
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.