Kotyla Przemysław, Gumkowska-Sroka Olga, Wnuk Bartosz, Kotyla Kacper
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.
Pharmaceuticals (Basel). 2022 Jul 28;15(8):936. doi: 10.3390/ph15080936.
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.
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。