Anifrolumab for refractory cutaneous lupus lesions in pediatric systemic lupus erythematosus

Type I interferon (IFN) plays an important role in the pathogenesis of systemic lupus erythematosus (SLE) and cutaneous manifestations. Anifrolumab, a fully humanized monoclonal antibody against type 1 IFN receptor, has shown a significant reduction of the disease activity of SLE and cutaneous manifestations in adults. We reported two pediatric SLE patients with refractory cutaneous lesions that dramatically improved after anifrolumab therapy. This is the first study to show clinical effects of anifrolumab for pediatric SLE patients. These cases suggest the efficacy of anifrolumab for pediatric SLE patients with refractory cutaneous lesions and elevated IFN levels.

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Publication Details

Journal
Lupus
Published
2025-03-23
DOI
https://doi.org/10.1177/09612033251330094
Citations
5
Primary Topic
Systemic Lupus Erythematosus Research
Type
article
Field-Weighted Citation Impact
8.34
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Anifrolumab for refractory cutaneous lupus lesions in pediatric systemic lupus erythematosus

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Anifrolumab for refractory cutaneous lupus lesions in pediatric systemic lupus erythematosus

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article en
5 citations

Abstract

Type I interferon (IFN) plays an important role in the pathogenesis of systemic lupus erythematosus (SLE) and cutaneous manifestations. Anifrolumab, a fully humanized monoclonal antibody against type 1 IFN receptor, has shown a significant reduction of the disease activity of SLE and cutaneous manifestations in adults. We reported two pediatric SLE patients with refractory cutaneous lesions that dramatically improved after anifrolumab therapy. This is the first study to show clinical effects of anifrolumab for pediatric SLE patients. These cases suggest the efficacy of anifrolumab for pediatric SLE patients with refractory cutaneous lesions and elevated IFN levels.

LupusVol. 34(5)
Tokyo Metropolitan Children's Medical Center (JP), Institute of Science Tokyo (JP)
Good health and well-being
Openalex Percentile: Top 2%
Systemic Lupus Erythematosus Research
8.34
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