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青少年系统性硬皮病的免疫发病机制。

Immunopathogenesis of Juvenile Systemic Sclerosis.

机构信息

Division of Rheumatology, Department of Pediatrics, University of Washington, Seattle, WA, United States.

Division of Pediatric Rheumatology, Department of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA, United States.

出版信息

Front Immunol. 2019 Jun 25;10:1352. doi: 10.3389/fimmu.2019.01352. eCollection 2019.

Abstract

Juvenile-onset systemic sclerosis (jSSc) is a rare and severe autoimmune disease with associated life-threatening organ inflammation and evidence of fibrosis. The organ manifestations of jSSc resemble adult SSc, but with better outcomes and survival. The etiology of jSSc appears to reflect adult-onset SSc, with similar inflammatory mediators and autoantibodies, but with a significant population of children with uncharacterized anti-nuclear antibodies. The genetics of patients with jSSc differ from women with SSc, resembling instead the genes of adult males with SSc, with additional HLA genes uniquely associated with childhood-onset disease. Current treatments are aimed at inhibiting the inflammatory aspect of disease, but important mechanisms of fibrosis regulated by dermal white adipose tissue dendritic cells may provide an avenue for targeting and potentially reversing the fibrotic stage.

摘要

青少年发病的系统性硬化症(jSSc)是一种罕见且严重的自身免疫性疾病,伴有危及生命的器官炎症和纤维化证据。jSSc 的器官表现类似于成人 SSc,但预后和存活率更好。jSSc 的病因似乎反映了成人发病的 SSc,具有相似的炎症介质和自身抗体,但有相当一部分儿童的抗核抗体特征不明。jSSc 患者的遗传学与 SSc 女性不同,更类似于成年男性 SSc 的基因,此外还存在与儿童发病疾病独特相关的 HLA 基因。目前的治疗方法旨在抑制疾病的炎症方面,但真皮白色脂肪组织树突状细胞调节的纤维化重要机制可能为靶向治疗并可能逆转纤维化阶段提供途径。

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