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Facial erythema after the treatment of dupilumab in SLE patient

BACKGROUND: Dupilumab is a receptor antagonist binding to the alpha subunit of the interleukin-4 receptor. Through binding to it, dupilumab inhibits signaling of both IL-4 and IL-13, the representative Th2 biomarkers. Recently, in addition to the treatment effects for atopic dermatitis (AD), there i...

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Autores principales: Jang, Dong Hyek, Lee, Jae In, Bae, Joo Yoon, Jung, Hye Jung, Park, Mi Yeon, Ahn, Jiyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491356/
https://www.ncbi.nlm.nih.gov/pubmed/32944024
http://dx.doi.org/10.1186/s13223-020-00458-6
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author Jang, Dong Hyek
Lee, Jae In
Bae, Joo Yoon
Jung, Hye Jung
Park, Mi Yeon
Ahn, Jiyoung
author_facet Jang, Dong Hyek
Lee, Jae In
Bae, Joo Yoon
Jung, Hye Jung
Park, Mi Yeon
Ahn, Jiyoung
author_sort Jang, Dong Hyek
collection PubMed
description BACKGROUND: Dupilumab is a receptor antagonist binding to the alpha subunit of the interleukin-4 receptor. Through binding to it, dupilumab inhibits signaling of both IL-4 and IL-13, the representative Th2 biomarkers. Recently, in addition to the treatment effects for atopic dermatitis (AD), there is an emerging adverse event as facial erythema. CASE PRESENTATION: A twenty-seven-year-old female patient developed erythema and desquamation on the face and neck after dupilumab administration. She had AD on her arms, legs, and trunk before the treatment but there was no atopic clinical feature in her face and neck. With the treatment of dupilumab, her skin lesions of the body have improved from the beginning of the treatment. In the patch test, including dupilumab, there was no specific finding other than the 1+ response to neomycin on day 2. In the intradermal test to dupilumab, a positive result was observed 15 min later, but negative both days 1 and 2. The blood examination showed an elevation of both ANA as 1:80 and anti-phospholipid antibodies (Anti-cardiolipin IgM, IgG, and Anti- beta 2 GPI IgG). She was diagnosed with Systemic lupus erythematosus (SLE) based on diagnostic criteria by a rheumatologist. CONCLUSION: Dupilumab is an emerging therapeutic agent for AD, and treatment cases are increasing in Korea. However, there are several adverse events during the treatment of dupilumab. Herein, we report the unexpected adverse event during the treatment of dupilumab in SLE patients.
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spelling pubmed-74913562020-09-16 Facial erythema after the treatment of dupilumab in SLE patient Jang, Dong Hyek Lee, Jae In Bae, Joo Yoon Jung, Hye Jung Park, Mi Yeon Ahn, Jiyoung Allergy Asthma Clin Immunol Case Report BACKGROUND: Dupilumab is a receptor antagonist binding to the alpha subunit of the interleukin-4 receptor. Through binding to it, dupilumab inhibits signaling of both IL-4 and IL-13, the representative Th2 biomarkers. Recently, in addition to the treatment effects for atopic dermatitis (AD), there is an emerging adverse event as facial erythema. CASE PRESENTATION: A twenty-seven-year-old female patient developed erythema and desquamation on the face and neck after dupilumab administration. She had AD on her arms, legs, and trunk before the treatment but there was no atopic clinical feature in her face and neck. With the treatment of dupilumab, her skin lesions of the body have improved from the beginning of the treatment. In the patch test, including dupilumab, there was no specific finding other than the 1+ response to neomycin on day 2. In the intradermal test to dupilumab, a positive result was observed 15 min later, but negative both days 1 and 2. The blood examination showed an elevation of both ANA as 1:80 and anti-phospholipid antibodies (Anti-cardiolipin IgM, IgG, and Anti- beta 2 GPI IgG). She was diagnosed with Systemic lupus erythematosus (SLE) based on diagnostic criteria by a rheumatologist. CONCLUSION: Dupilumab is an emerging therapeutic agent for AD, and treatment cases are increasing in Korea. However, there are several adverse events during the treatment of dupilumab. Herein, we report the unexpected adverse event during the treatment of dupilumab in SLE patients. BioMed Central 2020-07-03 /pmc/articles/PMC7491356/ /pubmed/32944024 http://dx.doi.org/10.1186/s13223-020-00458-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Jang, Dong Hyek
Lee, Jae In
Bae, Joo Yoon
Jung, Hye Jung
Park, Mi Yeon
Ahn, Jiyoung
Facial erythema after the treatment of dupilumab in SLE patient
title Facial erythema after the treatment of dupilumab in SLE patient
title_full Facial erythema after the treatment of dupilumab in SLE patient
title_fullStr Facial erythema after the treatment of dupilumab in SLE patient
title_full_unstemmed Facial erythema after the treatment of dupilumab in SLE patient
title_short Facial erythema after the treatment of dupilumab in SLE patient
title_sort facial erythema after the treatment of dupilumab in sle patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491356/
https://www.ncbi.nlm.nih.gov/pubmed/32944024
http://dx.doi.org/10.1186/s13223-020-00458-6
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