Eming R
Klinik für Dermatologie und Allergologie, Universitätsklinikum Gießen und Marburg GmbH, Standort Marburg, Baldingerstraße, 35043, Marburg, Deutschland,
Hautarzt. 2015 Aug;66(8):574-82. doi: 10.1007/s00105-015-3656-3.
Pemphigus is a severe bullous autoimmune dermatosis that represents a clinical challenge despite high-dose immunosuppressive therapy due to the therapy-related comorbidities and the lack of long-term control of disease activity.
Which targeted therapies are currently used in pemphigus and which innovative therapeutic strategies are in clinical development?
A review of the literature in PubMed was performed under consideration of the current guideline for the treatment of pemphigus as well as of our own results. Discussion of basic findings and results of targeted therapies in autoantibody-mediated autoimmune disorders were taken into account.
Immunapheresis and high-dose intravenous immunoglobulins with the aim of reducing circulating autoantibodies have been successfully used in the treatment of pemphigus. Depletion of autoreactive B-lymphocytes provides the rationale for the use of the monoclonal anti-CD20 antibody rituximab which demonstrated long-term clinical remission of pemphigus in clinical trials. Current developments include the investigation of humanised B-cell depleting antibodies in other B-cell driven autoimmune disorders as well as the identification of new cellular and molecular target structures that are essential in the humoral autoimmune cascade and exert important immune regulatory functions, respectively.
The well-characterised basic pathogenesis of pemphigus results in targeted therapies. Currently, therapies aiming at rapid reduction of circulating autoantibodies and the depletion of autoreactive B-cells are in clinical use. More cellular and molecular target structures are being investigated in other autoantibody-driven autoimmune disorders and they provide promising candidates for innovative pathogenesis-related therapeutic strategies in pemphigus in the future.
天疱疮是一种严重的大疱性自身免疫性皮肤病,尽管采用了高剂量免疫抑制治疗,但由于治疗相关的合并症以及疾病活动缺乏长期控制,仍是一项临床挑战。
目前天疱疮使用哪些靶向治疗方法,哪些创新治疗策略正在临床开发中?
根据天疱疮治疗的现行指南以及我们自己的研究结果,对PubMed中的文献进行了综述。考虑了自身抗体介导的自身免疫性疾病中靶向治疗的基本发现和结果。
旨在减少循环自身抗体的免疫吸附和高剂量静脉注射免疫球蛋白已成功用于天疱疮的治疗。自身反应性B淋巴细胞的清除为使用单克隆抗CD20抗体利妥昔单抗提供了理论依据,该抗体在临床试验中显示出天疱疮的长期临床缓解。当前的进展包括在其他B细胞驱动的自身免疫性疾病中研究人源化B细胞清除抗体,以及鉴定在体液自身免疫级联反应中至关重要且分别发挥重要免疫调节功能的新细胞和分子靶结构。
天疱疮明确的基本发病机制促成了靶向治疗。目前,旨在快速减少循环自身抗体和清除自身反应性B细胞的治疗方法正在临床应用中。在其他自身抗体驱动的自身免疫性疾病中正在研究更多的细胞和分子靶结构,它们为未来天疱疮创新的发病机制相关治疗策略提供了有前景的候选方案。