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系统性硬化症发病机制中的功能性自身抗体。

Functional autoantibodies in systemic sclerosis pathogenesis.

机构信息

Department of Rheumatology and Clinical Immunology, University Hospital Charité, Luisenstraße 13, 10117, Berlin, Germany,

出版信息

Curr Rheumatol Rep. 2015 May;17(5):34. doi: 10.1007/s11926-015-0505-4.

Abstract

Circulating antinuclear autoantibodies contribute to the diagnosis of systemic sclerosis (SSc) and correlate with disease-specific organ manifestations. Recent findings show the induction of interstitial lung disease and obliterative vasculopathy by transfer of IgG from SSc patients in healthy mice indicating a contribution of antibodies to SSc pathogenesis. Several functional or agonistic autoantibodies have been described in SSc, thus putting autoimmunity into a new spotlight. Autoantibodies against the angiotensin II receptor type-1 and the endothelin1 receptor type-A are associated with severe disease and provide new insights into its pathogenesis. They link the hallmarks of SSc, vasculopathy, immune activation, and fibrosis. At present, the contribution of the specific antibodies to disease manifestations remains to be examined. However; functional autoantibodies could represent a significant piece in the puzzle of SSc pathogenesis and may open new gateways and opportunities for therapeutic intervention. This review focuses on the features of functional autoantibodies in SSc.

摘要

循环抗核自身抗体有助于系统性硬化症 (SSc) 的诊断,并与特定于疾病的器官表现相关。最近的发现表明,通过将 SSc 患者的 IgG 转移到健康小鼠中,诱导了间质性肺病和闭塞性血管病,表明抗体对 SSc 发病机制有一定的贡献。在 SSc 中已经描述了几种功能或激动性自身抗体,因此将自身免疫置于新的焦点。针对血管紧张素 II 受体 1 型和内皮素 1 受体 A 型的自身抗体与严重疾病相关,并为其发病机制提供了新的见解。它们将 SSc 的特征、血管病变、免疫激活和纤维化联系起来。目前,特定抗体对疾病表现的贡献仍有待研究。然而,功能自身抗体可能是 SSc 发病机制之谜中的重要一环,并可能为治疗干预开辟新的途径和机会。本文重点介绍了 SSc 中功能自身抗体的特征。

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