Mesh : Humans Caspase 3 Alopecia / genetics Dermatitis Mutation Cicatrix / pathology

来  源:   DOI:10.1097/DAD.0000000000002428

Abstract:
UNASSIGNED: Central centrifugal cicatricial alopecia (CCCA) is a scarring alopecia that disproportionately affects patients with skin of color. Genetic studies have revealed that approximately 30% of CCCAs are associated with peptidyl arginine deiminase 3 misfolding mutations. Patients with CCCA usually have a poor prognosis with progressive and permanent hair loss. To further characterize CCCA, we evaluated the inflammatory milieu, PDL1, and caspase 3 expression. The data support the idea of CCCA being a CD4-predominant T-cell process. The loss of PDL1 and increase in caspase 3 expression raises the possibility of involvement of the PD1/PDL1 pathway in CCCA.
摘要:
中央离心性瘢痕性脱发(CCCA)是一种瘢痕性脱发,不成比例地影响肤色患者。遗传研究表明,大约30%的CCCA与肽基精氨酸脱亚胺酶3错误折叠突变有关。CCCA患者通常预后不良,进行性和永久性脱发。为了进一步表征CCCA,我们评估了炎症环境,PDL1和caspase3表达。数据支持CCCA是CD4占优势的T细胞过程的想法。PDL1的缺失和caspase3表达的增加增加了PD1/PDL1途径参与CCCA的可能性。
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