[Biologics for connective tissue diseases and vasculitides].

4区 医学 Q3 Medicine
Internist Pub Date : 2022-02-01 Epub Date: 2022-01-14 DOI:10.1007/s00108-021-01249-w
Bernhard Hellmich, Joerg C Henes
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引用次数: 0

Abstract

Despite therapy with glucocorticoids (GC) and conventional immunosuppressants, patients with connective tissue diseases and vasculitides often develop functionally relevant and prognostically unfavourable internal organ damage. Based on new pathogenetic insights, biologics and small molecules have recently been studied as targeted therapies for collagen vascular diseases and vasculitides. The B lymphocyte stimulator antagonist belimumab has been used for the treatment of systemic lupus erythematosus (SLE) for several years and has recently also been approved as an add-on therapy for lupus nephritis. Anifrolumab, an antibody against the type‑1 interferon receptor, has also been shown to be effective in phase III trials for the treatment of SLE. The interleukin (IL)-6-antagonist tocilizumab showed efficacy in the treatment of interstitial lung disease (ILD) in systemic sclerosis (SSc) and thus has been approved in the USA, although the phase III trial had a negative primary endpoint. In Europe the tyrosine inhibitor nintedanib is approved for progressive ILD in SSc. Tocilizumab is approved for the treatment of giant cell arteritis and reduces both the risk of recurrence and the cumulative GC requirement. The B‑lymphocyte depleting antibody rituximab is approved for induction and maintenance therapy of granulomatosis with polyangiitis and microscopic polyangiitis (MPA) and is currently also being investigated for the treatment of eosinophilic granulomatosis with polyangiitis (EGPA). In patients with EGPA, the IL‑5 antibody mepolizumab leads to improved disease control and reduces GC requirements. A phase III trial of the small molecule antagonist avacopan targeting the complement C5a receptor as a replacement for high-dose GC in induction therapy of GPA and MPA met its primary endpoints. Various other biologics and small molecule antagonists are currently in clinical development for several type of vasculitis and collagen vascular diseases, some of them at advanced stages.

[用于结缔组织疾病和血管疾病的生物制剂]。
尽管使用糖皮质激素(GC)和常规免疫抑制剂治疗,结缔组织疾病和血管血管炎患者经常发生功能相关和预后不利的内脏器官损伤。基于新的发病机制,生物制剂和小分子药物最近被研究作为胶原血管疾病和血管粥样硬化的靶向治疗。B淋巴细胞刺激拮抗剂belimumab已被用于治疗系统性红斑狼疮(SLE)多年,最近也被批准作为狼疮肾炎的附加治疗。Anifrolumab是一种针对1型干扰素受体的抗体,在治疗SLE的III期试验中也被证明是有效的。白细胞介素(IL)-6拮抗剂tocilizumab在治疗系统性硬化症(SSc)的间质性肺疾病(ILD)中显示出疗效,因此已在美国获得批准,尽管III期试验的主要终点为阴性。在欧洲,酪氨酸抑制剂尼达尼布被批准用于治疗SSc的进行性ILD。Tocilizumab被批准用于治疗巨细胞动脉炎,可降低复发风险和累积GC要求。B淋巴细胞消耗抗体美罗华(rituximab)被批准用于诱导和维持治疗肉芽肿病合并多血管炎和显微多血管炎(MPA),目前也正在研究治疗嗜酸性肉芽肿病合并多血管炎(EGPA)。在EGPA患者中,IL - 5抗体mepolizumab可改善疾病控制并降低GC需求。一项针对补体C5a受体的小分子拮抗剂avacopan在GPA和MPA诱导治疗中替代大剂量GC的III期试验达到了主要终点。各种其他生物制剂和小分子拮抗剂目前正在临床开发中,用于几种类型的血管炎和胶原血管疾病,其中一些已进入晚期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Internist
Internist 医学-医学:内科
CiteScore
1.20
自引率
0.00%
发文量
139
审稿时长
4-8 weeks
期刊介绍: Der Internist is an internationally respected journal dealing with all aspects of internal medicine. The journal serves both the scientific exchange and the continuing education of internists working in practical or clinical environments as well as of general practitioners who are particularly interested in internal medicine. The focus is on the topics of prevention, diagnostic approaches, management of complications, and current therapy strategies. Comprehensive reviews on a specific topical issue focus on providing evidenced based information on diagnostics and therapy. Case reports feature interesting cases and aim at optimizing diagnostic and therapeutic strategies. Review articles under the rubric "Continuing Medical Education" present verified results of scientific research and their integration into daily practice.
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