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CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab

CARD14-associated papulosquamous eruption is an autosomal dominant genodermatosis characterized by early-onset, generalized erythematous patches and plaques with prominent scales, mostly with facial involvement. Heterozygous gain-of-function variants in the CARD14 gene have been reported to be causa...

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Detalles Bibliográficos
Autores principales: Dai, Shangzhi, Zhang, Shanshan, Wang, Chenliang, Lin, Xin, Lin, Zhimiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868849/
https://www.ncbi.nlm.nih.gov/pubmed/36699196
http://dx.doi.org/10.1016/j.xjidi.2022.100174
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author Dai, Shangzhi
Zhang, Shanshan
Wang, Chenliang
Lin, Xin
Lin, Zhimiao
author_facet Dai, Shangzhi
Zhang, Shanshan
Wang, Chenliang
Lin, Xin
Lin, Zhimiao
author_sort Dai, Shangzhi
collection PubMed
description CARD14-associated papulosquamous eruption is an autosomal dominant genodermatosis characterized by early-onset, generalized erythematous patches and plaques with prominent scales, mostly with facial involvement. Heterozygous gain-of-function variants in the CARD14 gene have been reported to be causative for this entity. The pathogenesis mainly involves the IL-23‒IL-17 inflammatory circuit, yet the efficacy of anti‒IL-17 treatment remained less examined. In this study, we report one previously unidentified variant underlying the CARD14-associated papulosquamous eruption and showed its gain-of-function property. Furthermore, we present the beneficial effect of anti‒IL-17A treatment in our patient.
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spelling pubmed-98688492023-01-24 CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab Dai, Shangzhi Zhang, Shanshan Wang, Chenliang Lin, Xin Lin, Zhimiao JID Innov Original Article CARD14-associated papulosquamous eruption is an autosomal dominant genodermatosis characterized by early-onset, generalized erythematous patches and plaques with prominent scales, mostly with facial involvement. Heterozygous gain-of-function variants in the CARD14 gene have been reported to be causative for this entity. The pathogenesis mainly involves the IL-23‒IL-17 inflammatory circuit, yet the efficacy of anti‒IL-17 treatment remained less examined. In this study, we report one previously unidentified variant underlying the CARD14-associated papulosquamous eruption and showed its gain-of-function property. Furthermore, we present the beneficial effect of anti‒IL-17A treatment in our patient. Elsevier 2022-12-11 /pmc/articles/PMC9868849/ /pubmed/36699196 http://dx.doi.org/10.1016/j.xjidi.2022.100174 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Dai, Shangzhi
Zhang, Shanshan
Wang, Chenliang
Lin, Xin
Lin, Zhimiao
CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab
title CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab
title_full CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab
title_fullStr CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab
title_full_unstemmed CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab
title_short CARD14 Missense Variant Underlying CARD14-Associated Papulosquamous Eruption with Beneficial Response to Secukinumab
title_sort card14 missense variant underlying card14-associated papulosquamous eruption with beneficial response to secukinumab
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868849/
https://www.ncbi.nlm.nih.gov/pubmed/36699196
http://dx.doi.org/10.1016/j.xjidi.2022.100174
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