医学
银屑病
免疫缺陷
病因学
皮肤病科
联机孟德尔在人类中的遗传
泛发性脓疱性银屑病
脓疱性银屑病
红皮病
免疫学
生物
遗传学
病理
免疫系统
基因
表型
作者
Piranit Nik Kantaputra,Suteeraporn Chaowattanapanit,Salin Kiratikanon,Romanee Chaiwarith,Charoen Choonhakarn,Worrachet Intachai,Natalina Quarto,Sissades Tongsima,James R. Ketudat Cairns,Chumpol Ngamphiw,John J. McGrath,Mati Chuamanochan
标识
DOI:10.1111/1346-8138.16081
摘要
Adult-onset immunodeficiency syndrome (AOID) with anti-interferon (IFN)-γ autoantibodies is characterized by an AIDS-like illness with disruptive IFN-γ signaling. Patients generally present with recurrent and disseminated opportunistic infections along with neutrophilic dermatoses. Generalized pustular psoriasis (GPP; Online Mendelian Inheritance in Man #614204) is characterized by acute generalized erythema and scaling with numerous aseptic pustules. Mutations in SERPINA3 have been reported as predisposing risk factors for both AOID and GPP. Here, we report two unrelated patients, one with AOID and a pustular skin reaction and the other with GPP, who both carried the same heterozygous variant c.718G>A (p.Val240Met) in SERPINA1. Our observation of a shared mutation in SERPINA1 in AOID and GPP indicate possible pathobiological and disease mechanism similarities in these two disorders. Thus, variants in both SERPINA1, SERPINA3, and potentially other SERPIN family members may be associated with the etiology of GPP and AOID.
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