Protein kinases: drug targets for immunological disorders

被引:43
作者
Castelo-Soccio, Leslie [1 ]
Kim, Hanna [2 ]
Gadina, Massimo [3 ]
Schwartzberg, Pamela L. [4 ]
Laurence, Arian [5 ,6 ]
O'Shea, John J. [7 ]
机构
[1] Natl Inst Arthrit & Musculoskeletal & Skin Dis, Dermatol Branch, NIH, Bethesda, MD USA
[2] Natl Inst Arthrit & Musculoskeletal & Skin Dis, Juvenile Myositis Pathogenesis & Therapeut Unit, NIH, Bethesda, MD USA
[3] Natl Inst Arthrit & Musculoskeletal & Skin Dis, Translat Immunol Sect, NIH, Bethesda, MD USA
[4] Natl Inst Allergy & Infect Dis, NIH, Bethesda, MD USA
[5] Royal Free London Hosp NHS Fdn Trust, Dept Immunol, London, England
[6] Univ Coll London Hosp NHS Fdn Trust, London, England
[7] Natl Inst Arthrit & Musculoskeletal & Skin Dis, Mol Immunol & Inflammat Branch, NIH, Bethesda, MD USA
关键词
ACTIVE RHEUMATOID-ARTHRITIS; TYROSINE KINASE; ALOPECIA-AREATA; OPEN-LABEL; CALCINEURIN INHIBITORS; TOFACITINIB CP-690,550; MAINTENANCE THERAPY; IMPROVED SURVIVAL; JAK INHIBITION; CELL-RECEPTOR;
D O I
10.1038/s41577-023-00877-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Drugs that target protein kinases have had a major impact on the treatment of cancer and now are proving beneficial in numerous immunological diseases. This Review describes their clinical application, with a focus on Janus kinase inhibitors, and how they inform mechanisms of disease and have evolved to improve efficacy and safety. Protein kinases play a major role in cellular activation processes, including signal transduction by diverse immunoreceptors. Given their roles in cell growth and death and in the production of inflammatory mediators, targeting kinases has proven to be an effective treatment strategy, initially as anticancer therapies, but shortly thereafter in immune-mediated diseases. Herein, we provide an overview of the status of small molecule inhibitors specifically generated to target protein kinases relevant to immune cell function, with an emphasis on those approved for the treatment of immune-mediated diseases. The development of inhibitors of Janus kinases that target cytokine receptor signalling has been a particularly active area, with Janus kinase inhibitors being approved for the treatment of multiple autoimmune and allergic diseases as well as COVID-19. In addition, TEC family kinase inhibitors (including Bruton's tyrosine kinase inhibitors) targeting antigen receptor signalling have been approved for haematological malignancies and graft versus host disease. This experience provides multiple important lessons regarding the importance (or not) of selectivity and the limits to which genetic information informs efficacy and safety. Many new agents are being generated, along with new approaches for targeting kinases.
引用
收藏
页码:787 / 806
页数:20
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