Pathophysiology of generalized pustular psoriasis

被引:16
|
作者
Young, Kelly Z. [1 ]
Sarkar, Mrinal K. [2 ]
Gudjonsson, Johann E. [2 ,3 ]
机构
[1] Univ Michigan, Med Sch, Ann Arbor, MI USA
[2] Univ Michigan, Dept Dermatol, Ann Arbor, MI USA
[3] Univ Michigan, Taubman Ctr 1910, Dept Dermatol, 1500 E Med Ctr Dr, Ann Arbor, MI 48109 USA
关键词
autoinflammation; generalized pustular psoriasis; genetics; IL-36; psoriasis vulgaris; ANTAGONIST DEFICIENCY; AP1S3; MUTATIONS; PATIENT; DISEASE; IL-36; LEUKOCYTES; AUTOPHAGY; DIAGNOSIS; VULGARIS; PATHWAY;
D O I
10.1111/exd.14768
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Psoriasis is a chronic, immune-mediated skin disease that affects over 3% of adults in the United States. Psoriasis can present in several clinical forms. Of these, generalized pustular psoriasis is an acute, severe form, associated with increased morbidity and mortality. Unlike the more common plaque psoriasis, which is thought to feature dysregulation of the adaptive immune system, generalized pustular psoriasis reflects heightened autoinflammatory responses. Recent advances in genetic and immunological studies highlight a key role of the IL-36 immune axis in the pathogenesis of generalized pustular psoriasis. In this article, we review the psoriatic subtypes and discuss diagnostic criteria of generalized pustular psoriasis, discuss several newly identified genetic variants associated with pustular disease in the skin, and discuss how these mutations shed light on pustular disease mechanisms. Furthermore, we gather insights from recent transcriptomic studies that similarly implicate a pathogenic role of the IL-36 immune axis in generalized pustular psoriasis.
引用
收藏
页码:1194 / 1203
页数:10
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