Suppr超能文献

用于治疗自身免疫性疾病的Jak抑制剂:来自系统性硬化症和系统性红斑狼疮的经验教训。

Jak Inhibitors for Treatment of Autoimmune Diseases: Lessons from Systemic Sclerosis and Systemic Lupus Erythematosus.

作者信息

Kotyla Przemysław, Gumkowska-Sroka Olga, Wnuk Bartosz, Kotyla Kacper

机构信息

Department of Internal Medicine, Rheumatology and Clinical Immunology Medical University of Silesia, 40-635 Katowice, Poland.

Department of Rheumatology, Voivodeship Hospital No. 5, 41-200 Sosnowiec, Poland.

出版信息

Pharmaceuticals (Basel). 2022 Jul 28;15(8):936. doi: 10.3390/ph15080936.

Abstract

Systemic sclerosis and systemic lupus erythematosus represent two distinct autoimmune diseases belonging to the group of connective tissue disorders. Despite the great progress in the basic science, this progress has not been translated to the development of novel therapeutic approaches that can radically change the face of these diseases. The discovery of JAK kinases, which are tyrosine kinases coupled with cytokine receptors, may open a new chapter in the treatment of so far untreatable diseases. Small synthetic compounds that can block Janus kinases and interact directly with cytokine signalling may provide therapeutic potential in these diseases. In this review, we discuss the therapeutic potential of Jak kinases in light of the cytokine network that JAK kinases are able to interact with. We also provide the theoretical background for the rationale of blocking cytokines with specific JAK inhibitors.

摘要

系统性硬化症和系统性红斑狼疮是结缔组织疾病中的两种不同的自身免疫性疾病。尽管基础科学取得了巨大进展,但这一进展尚未转化为能够从根本上改变这些疾病面貌的新型治疗方法的开发。与细胞因子受体偶联的酪氨酸激酶——JAK激酶的发现,可能为迄今无法治疗的疾病的治疗开启新篇章。能够阻断Janus激酶并直接与细胞因子信号传导相互作用的小分子合成化合物,可能在这些疾病中具有治疗潜力。在本综述中,我们根据JAK激酶能够与之相互作用的细胞因子网络,讨论JAK激酶的治疗潜力。我们还为使用特异性JAK抑制剂阻断细胞因子的原理提供了理论背景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b354/9413112/244b36f02a0f/pharmaceuticals-15-00936-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验