{"title":"CS12192选择性靶向JAK3/JAK1/TBK1逆转斑秃","authors":"Heping Jin, Zongyang Li, Xinwen Li, Qiongqiong Xu, Beizhong Chen, Song Shan, Desi Pan, Peng Hu, Shengjian Huang","doi":"10.1002/adbi.202400769","DOIUrl":null,"url":null,"abstract":"<p>The approval of JAK inhibitors, represented by baricitinib, for the treatment of alopecia areata (AA) has ushered in a new era. However, their excessive immunosuppressive effects have also raised numerous concerns. Therefore, the development of JAK inhibitors with different selectivities may enhance drug safety while maintaining therapeutic efficacy. CS12192, developed by our team, is a selective JAK3 inhibitor that also partially inhibits JAK1 and TBK1. In this study, we evaluate the effectiveness of CS12192 and baricitinib in a C3H/HeJ skin-transplanted AA mouse model and conduct in-depth analysis of the similarities and differences in the mechanisms of the two compounds using mass cytometry (CyTOF) and RNA-seq technology. The results show that CS12192 could reverse hair growth inhibition in AA mice in a dose-dependent manner, with the high-dose group exhibiting comparable effectiveness to baricitinib but with better safety. Further research revealed that both compounds significantly reduced the infiltration of immune cells, particularly CD8<sup>+</sup> T cells, in the skin of AA animals. CyTOF and RNA-seq analysis revealed the mechanistic similarities between CS12192 and baricitinib in regulating AA-related immune cells and signaling pathways. In conclusion, CS12192, as a novel selective JAK inhibitor, holds great potential for the treatment of AA.</p>","PeriodicalId":7234,"journal":{"name":"Advanced biology","volume":"9 8","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CS12192 Reverses Alopecia Areata by Selectively Targeting JAK3/JAK1/TBK1\",\"authors\":\"Heping Jin, Zongyang Li, Xinwen Li, Qiongqiong Xu, Beizhong Chen, Song Shan, Desi Pan, Peng Hu, Shengjian Huang\",\"doi\":\"10.1002/adbi.202400769\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The approval of JAK inhibitors, represented by baricitinib, for the treatment of alopecia areata (AA) has ushered in a new era. However, their excessive immunosuppressive effects have also raised numerous concerns. Therefore, the development of JAK inhibitors with different selectivities may enhance drug safety while maintaining therapeutic efficacy. CS12192, developed by our team, is a selective JAK3 inhibitor that also partially inhibits JAK1 and TBK1. In this study, we evaluate the effectiveness of CS12192 and baricitinib in a C3H/HeJ skin-transplanted AA mouse model and conduct in-depth analysis of the similarities and differences in the mechanisms of the two compounds using mass cytometry (CyTOF) and RNA-seq technology. The results show that CS12192 could reverse hair growth inhibition in AA mice in a dose-dependent manner, with the high-dose group exhibiting comparable effectiveness to baricitinib but with better safety. Further research revealed that both compounds significantly reduced the infiltration of immune cells, particularly CD8<sup>+</sup> T cells, in the skin of AA animals. CyTOF and RNA-seq analysis revealed the mechanistic similarities between CS12192 and baricitinib in regulating AA-related immune cells and signaling pathways. In conclusion, CS12192, as a novel selective JAK inhibitor, holds great potential for the treatment of AA.</p>\",\"PeriodicalId\":7234,\"journal\":{\"name\":\"Advanced biology\",\"volume\":\"9 8\",\"pages\":\"\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adbi.202400769\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced biology","FirstCategoryId":"99","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adbi.202400769","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
摘要
以巴利昔尼(baricitinib)为代表的 JAK 抑制剂获批用于治疗斑秃(AA)开创了一个新时代。然而,其过度的免疫抑制作用也引发了许多担忧。因此,开发具有不同选择性的JAK抑制剂可以在保证疗效的同时提高药物的安全性。我们团队开发的 CS12192 是一种选择性 JAK3 抑制剂,它也能部分抑制 JAK1 和 TBK1。在本研究中,我们评估了 CS12192 和巴利昔尼在 C3H/HeJ 皮肤移植 AA 小鼠模型中的疗效,并利用质量细胞计(CyTOF)和 RNA-seq 技术深入分析了两种化合物作用机制的异同。结果显示,CS12192能以剂量依赖的方式逆转AA小鼠的毛发生长抑制,其中高剂量组的有效性与巴利替尼相当,但安全性更好。进一步的研究发现,这两种化合物都能显著减少 AA 动物皮肤中免疫细胞的浸润,尤其是 CD8+ T 细胞。CyTOF和RNA-seq分析揭示了CS12192和巴利替尼在调节AA相关免疫细胞和信号通路方面的机理相似性。总之,CS12192作为一种新型选择性JAK抑制剂,在治疗AA方面具有巨大潜力。
CS12192 Reverses Alopecia Areata by Selectively Targeting JAK3/JAK1/TBK1
The approval of JAK inhibitors, represented by baricitinib, for the treatment of alopecia areata (AA) has ushered in a new era. However, their excessive immunosuppressive effects have also raised numerous concerns. Therefore, the development of JAK inhibitors with different selectivities may enhance drug safety while maintaining therapeutic efficacy. CS12192, developed by our team, is a selective JAK3 inhibitor that also partially inhibits JAK1 and TBK1. In this study, we evaluate the effectiveness of CS12192 and baricitinib in a C3H/HeJ skin-transplanted AA mouse model and conduct in-depth analysis of the similarities and differences in the mechanisms of the two compounds using mass cytometry (CyTOF) and RNA-seq technology. The results show that CS12192 could reverse hair growth inhibition in AA mice in a dose-dependent manner, with the high-dose group exhibiting comparable effectiveness to baricitinib but with better safety. Further research revealed that both compounds significantly reduced the infiltration of immune cells, particularly CD8+ T cells, in the skin of AA animals. CyTOF and RNA-seq analysis revealed the mechanistic similarities between CS12192 and baricitinib in regulating AA-related immune cells and signaling pathways. In conclusion, CS12192, as a novel selective JAK inhibitor, holds great potential for the treatment of AA.