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Recent progress on tyrosine kinase 2 JH2 inhibitors
被引:7
|作者:
Deng, Lidan
[1
]
Wan, Li
[1
]
Liao, Tingting
[2
]
Wang, Lin
[3
]
Wang, Jie
[4
]
Wu, Xianbo
[1
]
Shi, Jianyou
[1
,5
,6
,7
]
机构:
[1] Chengdu Sport Univ, Sch Sports Med & Hlth, Chengdu 610041, Sichuan, Peoples R China
[2] Hosp Chengdu Univ Tradit Chinese Med, Chengdu 610072, Sichuan, Peoples R China
[3] Xihua Univ, Coll Food & Bioengn, Chengdu 610039, Peoples R China
[4] Guizhou Univ Tradit Chinese Med, Guiyang 550002, Guizhou, Peoples R China
[5] Univ Elect Sci & Technol China, Sichuan Acad Med Sci, Dept Pharm,Sch Med, Personalized Drug Therapy Key Lab Sichuan Prov, Chengdu 610072, Sichuan, Peoples R China
[6] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Sch Med, Chengdu 610072, Sichuan, Peoples R China
[7] Chengdu Univ Tradit Chinese Med, State Key Lab Southwestern Chinese Med Resources, Chengdu 611137, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Tyrosine kinase 2 (TYK2);
JH2;
inhibitor;
Autoimmune diseases;
Deucravacitinib;
BMS-986202;
SYSTEMIC-LUPUS-ERYTHEMATOSUS;
PSORIATIC-ARTHRITIS;
CLINICAL-FEATURES;
JAK INHIBITORS;
JANUS KINASES;
IMMUNE;
MECHANISMS;
DISCOVERY;
STATS;
EPIDEMIOLOGY;
D O I:
10.1016/j.intimp.2023.110434
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Tyrosine kinase 2 (TYK2) is a member of the Janus kinase (JAK) family, which can regulate the signaling of multiple pro-inflammatory cytokines, including IL12, IL23 and type I interferon (IFN & alpha;/& beta;), and its inhibitors can treat autoimmune diseases caused by the abnormal expression of IL12 and IL23. Interest in TYK2 JH2 inhibitors has increased as a result of safety concerns with JAK inhibitors. This overview introduces TYK2 JH2 inhibitors that are already on the market, including Deucravactinib (BMS-986165), as well as those currently in clinical trials, such as BMS-986202, NDI-034858, and ESK-001.
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页数:10
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