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[系统性硬化症发病机制的更新:迈向新的治疗机遇]

[Updates in systemic sclerosis pathogenesis: Toward new therapeutic opportunities].

作者信息

Didier K, Robbins A, Antonicelli F, Pham B N, Giusti D, Servettaz A

机构信息

Service de médecine interne, maladies infectieuses et immunologie clinique, faculté de médecine de Reims, CHU de Reims, 51100 Reims, France; EA 7509 Immuno-régulation et remodelage tissulaire dans le cancer et dans les maladies auto-immunes et inflammatoires, université Reims Champagne Ardenne, 51100 Reims, France.

EA 7509 Immuno-régulation et remodelage tissulaire dans le cancer et dans les maladies auto-immunes et inflammatoires, université Reims Champagne Ardenne, 51100 Reims, France.

出版信息

Rev Med Interne. 2019 Oct;40(10):654-663. doi: 10.1016/j.revmed.2019.05.016. Epub 2019 Jul 11.

Abstract

Systemic sclerosis is a rare connective tissue disease characterized by skin and several internal organ fibrosis, systemic vasculopathy and immune abnormalities. Even if fibroblasts and endothelial cells dysfunction, as well as lymphocytes and other immune cells implication are now well described, the exact origin and chronology of the disease pathogenesis remain unclear. Oxidative stress, influenced by genetic and environmental factors, seems to play a key role. Indeed, it seems to be implicated in the early phases of fibrosis development, vasculopathy and in immune tolerance abnormalities shared by all patients, although disease expression is heterogeneous. To date, no curative treatment is available. Even if immunosuppressive treatment or drugs acting on vascular system are proposed for some patients, overall, treatment efficiency remains modest. Only autologous hematopoietic stem cells transplantation, reserved for patients with severe or rapidly progressive fibrosis, has recently demonstrated efficiency, with lasting regression of fibrosis. Nevertheless, this treatment can expose to important, life-threatening toxicity. In the last decade, new mechanisms implicated in the pathogenesis of systemic sclerosis have been unraveled, bringing new therapeutic opportunities. In this review, we offer to focus on recent insights in the knowledge of systemic sclerosis pathogenesis and its implication in current and future medical care.

摘要

系统性硬化症是一种罕见的结缔组织疾病,其特征为皮肤和多个内脏器官纤维化、系统性血管病变及免疫异常。尽管目前对成纤维细胞和内皮细胞功能障碍以及淋巴细胞和其他免疫细胞的参与情况已有充分描述,但该疾病发病机制的确切起源和时间顺序仍不清楚。受遗传和环境因素影响的氧化应激似乎起着关键作用。事实上,氧化应激似乎与纤维化发展的早期阶段、血管病变以及所有患者共有的免疫耐受异常有关,尽管疾病表现具有异质性。迄今为止,尚无治愈性治疗方法。即使对一些患者采用免疫抑制治疗或作用于血管系统的药物,但总体而言,治疗效果仍较为有限。只有自体造血干细胞移植(仅适用于重度或快速进展性纤维化患者)最近显示出疗效,纤维化可持久消退。然而,这种治疗可能会带来严重的、危及生命的毒性。在过去十年中,已揭示出系统性硬化症发病机制中的新机制,带来了新的治疗机会。在本综述中,我们将重点关注系统性硬化症发病机制的最新见解及其在当前和未来医疗中的意义。

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