Evidence map›Paper›PMID 40176112›Full record

ArticleOrphanet journal of rare diseases2025

Tofacitinib treatment for psoriatic skin lesions associated with Aicardi-Goutières syndrome 7/Singleton-Merten syndrome 1.

Shanice Beerepoot, Lucas Grinwis, Adeline L Vanderver, Marjo S van der Knaap, Taco W Kuijpers

Abstract readCase ReportsLetter
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. medRxiv : the preprint server for health sciences · 2026
    Article
  2. Article
  3. A review of core immuno-inflammatory mechanisms and key regulatory targets in psoriasis.American journal of clinical and experimental immunology · 2026
    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

5 authors.

Shanice BeerepootDepartment of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children'S Hospital, Amsterdam University Medical Centers, VU University, 1081 HV, Amsterdam, The Netherlands.
Lucas GrinwisDepartment of Pediatric Immunology, Rheumatology and Infectious Diseases, Amsterdam University Medical Centers, Emma Children'S Hospital, University of Amsterdam, Amsterdam, The Netherlands.
Adeline L VanderverDivision of Neurology, The Children'S Hospital of Philadelphia, Philadelphia, PA, USA.
Marjo S van der KnaapDepartment of Child Neurology, Amsterdam Leukodystrophy Center, Emma Children'S Hospital, Amsterdam University Medical Centers, VU University, 1081 HV, Amsterdam, The Netherlands.
Taco W KuijpersDepartment of Pediatric Immunology, Rheumatology and Infectious Diseases, Amsterdam University Medical Centers, Emma Children'S Hospital, University of Amsterdam, Amsterdam, The Netherlands. t.w.kuijpers@amsterdamumc.nl.ORCID http://orcid.org/0000-0002-7421-3370

Funding

Clinical Outcomes in Aicardi Goutières SyndromeU01NS106845 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI VANDERVER, ADELINE LUCIE · 2019 to 2023
$7.5M
NINDS NIH HHS U01 NS106845NINDS NIH HHS U01NS106845
6 · The paper itself

Abstract

The purpose of this letter to the editor is to illustrate the effect of tofacitinib on psoriatic skin lesions in a patient with Aicardi-Goutières syndrome (AGS) type 7/Singleton-Merten syndrome 1. AGS is characterized by an encephalopathy of variable severity and systemic autoinflammatory manifestations due to continuous type I interferon (IFN) induction. While traditional JAK 1/2 inhibitors like baricitinib and ruxolitinib have proven effectiveness for systemic inflammatory symptoms, they face reimbursement issues in some countries. Tofacitinib, a JAK 1/3 inhibitor, significantly improved psoriatic skin lesions in our patient without the need for additional immunosuppressive therapy. Within one month of starting tofacitinib, psoriatic rashes and ulcerative skin lesions markedly improved, in the absence of a reduction in the IFN-stimulated gene signature or CD169 expression on monocytes. The clinical benefits persisted until the treatment was discontinued, after which symptoms recurred. Resuming tofacitinib treatment again led to improvement. No adverse effects were observed. This case highlights the potential of tofacitinib as a clinically effective treatment for psoriatic skin lesions in AGS and offers a viable alternative for JAK 1/2 inhibitors for this target symptom. Further studies are needed to confirm the long-term safety of JAK 1/3 inhibitors in AGS as well as their possible efficacy and dosing to address other systemic symptoms or neurologic manifestations.

Indexed as

Autoimmune Diseases of the Nervous SystemCerebellumNervous System MalformationsOdontodysplasiaPiperidinesProtein Kinase InhibitorsPsoriasisPyrimidinesPyrrolesAortic DiseasesDental Enamel HypoplasiaFemaleHumansMaleMetacarpusMuscular DiseasesPiperidinesProtein Kinase InhibitorsPyrimidinesPyrrolestofacitinibAicardi-Goutières syndrome 7InterferonopathyJanus kinase (JAK) inhibitorSingleton-Merten syndrome 1Tofacitinib

Identifiers

PMID40176112
PMCPMC11967008

What OpenQuestion holds

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Registered trials

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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.