Similar Molecular Features in Two Cases of <scp>CARD14</scp>‐Associated Papulosquamous Eruption

Subjects carrying variants in the caspase recruitment domain family member 14 (CARD14) gene can exhibit characteristics of psoriasis and pityriasis rubra pilaris (PRP). The term 'CARD14-associated papulosquamous eruption (CAPE)' is used to describe individuals presenting with symptoms of both conditions. This study aimed to diagnose two cases of CAPE and explore the pathogenic mechanisms, including inflammatory trends and differential features. Whole-exome sequencing and Sanger sequencing identified a novel variant, c.2768T>C and a recurrent variant, c.467T>C, in CARD14 in two unrelated individuals, both exhibiting incomplete penetrance. Both of patients exhibited increased IL-17A in skin lesions, but not in serum, potentially explaining the reported cases with low response rate to secukinumab. One patient also exhibited increased IL-23A in serum. Additionally, the epidermis of lesions showed aberrant late differentiation and active NF-κB signalling.

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Publication Details

Journal
Australasian Journal of Dermatology
Published
2025-03-14
DOI
https://doi.org/10.1111/ajd.14455
Citations
2
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
4.01

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article

Similar Molecular Features in Two Cases of CARD14‐Associated Papulosquamous Eruption

Yumeng Wang, Haifei Liu, Bing Wang, Jiawen Chen et al.
2 citations
Australasian Journal of Dermatology
Dermatology and Skin Diseases
4.01
article

Similar Molecular Features in Two Cases of CARD14‐Associated Papulosquamous Eruption

Yumeng Wang, Haifei Liu, Bing Wang, Jiawen Chen, Ming Li, Zhirong Yao, Xiaobo Feng, Jinxiang Yang, Fuh‐Miin Liang
article en
2 citations

Abstract

Subjects carrying variants in the caspase recruitment domain family member 14 (CARD14) gene can exhibit characteristics of psoriasis and pityriasis rubra pilaris (PRP). The term 'CARD14-associated papulosquamous eruption (CAPE)' is used to describe individuals presenting with symptoms of both conditions. This study aimed to diagnose two cases of CAPE and explore the pathogenic mechanisms, including inflammatory trends and differential features. Whole-exome sequencing and Sanger sequencing identified a novel variant, c.2768T>C and a recurrent variant, c.467T>C, in CARD14 in two unrelated individuals, both exhibiting incomplete penetrance. Both of patients exhibited increased IL-17A in skin lesions, but not in serum, potentially explaining the reported cases with low response rate to secukinumab. One patient also exhibited increased IL-23A in serum. Additionally, the epidermis of lesions showed aberrant late differentiation and active NF-κB signalling.

Australasian Journal of DermatologyVol. 66(3)
Shanghai Jiao Tong University (CN), XinHua Hospital (CN), Children's Hospital of Fudan University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 8%
Dermatology and Skin Diseases
4.01
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