Sustained Interferon Signature Suppression With Anifrolumab in a Patient With STING‐Associated Vasculopathy with Onset in Infancy Refractory to <scp>JAK</scp> Inhibitor and Dazukibart Therapy

This case underscores the challenges in treating patients with SAVI and highlights the utility of IFN I scores as a theragnostic biomarker. Although high-dose JAKi and dazukibart failed to achieve sustained control of IFN I signaling, treatment with anifrolumab durably suppressed IFN scores and demonstrated promising efficacy, which allows for the investigation of the role of IFN I signaling in the disease pathogenesis of SAVI and other interferonopathies in future clinical trials.

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Publication Details

Journal
Arthritis & Rheumatology
Published
2025-03-11
DOI
https://doi.org/10.1002/art.43145
Citations
8
Primary Topic
Cytokine Signaling Pathways and Interactions
Type
article
Field-Weighted Citation Impact
8.36

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article

Sustained Interferon Signature Suppression With Anifrolumab in a Patient With STING‐Associated Vasculopathy with Onset in Infancy Refractory to JAK Inhibitor and Dazukibart Therapy

Oluwatobi Arisa, Douglas B. Kuhns, Sara Alehashemi, Cody J. Peer et al.
8 citations
Arthritis & Rheumatology
Cytokine Signaling Pathways and Interactions
8.36
article

Sustained Interferon Signature Suppression With Anifrolumab in a Patient With STING‐Associated Vasculopathy with Onset in Infancy Refractory to JAK Inhibitor and Dazukibart Therapy

Oluwatobi Arisa, Douglas B. Kuhns, Sara Alehashemi, Cody J. Peer, Raphaela Goldbach‐Mansky, Danielle Fink, Adriana A. de Jesus, William D. Figg, Bjoern Buehring, Andre Rastegar, Ben Colton, Kip Friend, Sachin Gaurav, Alexi Baumgardner
article en
8 citations

Abstract

This case underscores the challenges in treating patients with SAVI and highlights the utility of IFN I scores as a theragnostic biomarker. Although high-dose JAKi and dazukibart failed to achieve sustained control of IFN I signaling, treatment with anifrolumab durably suppressed IFN scores and demonstrated promising efficacy, which allows for the investigation of the role of IFN I signaling in the disease pathogenesis of SAVI and other interferonopathies in future clinical trials.

Arthritis & RheumatologyVol. 77(8)
University of Wuppertal (DE), Frederick National Laboratory for Cancer Research (US), National Institute of Allergy and Infectious Diseases (US), National Cancer Institute (US), National Institutes of Health Clinical Center (US)
Pfizer, National Institutes of Health
Openalex Percentile: Top 2%
Cytokine Signaling Pathways and Interactions
8.36
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