Journal
TRANSFUSION MEDICINE REVIEWS
Volume 36, Issue 4, Pages 239-245Publisher
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.tmrv.2022.06.009
Keywords
Bruton tyrosine kinase; Immune thrombocytopenia; Autoimmune haematology; Autoimmune hemolytic anaemia; Rilzabrutinib; Ibrutinib; BTK inhibitors; BTKi; BTK; ITP; AIHA
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Autoreactive B-cells play a crucial role in the development of autoimmune disorders, and therapies targeting these cells, such as BTK inhibitors, have shown promise in treating autoimmune haematologic conditions.
Autoreactive B-cells are crucial in the pathogenesis of both haematologic and non-haematologic autoim-mune disorders. Therapies targeting B cells and autoantibodies are widely used in clinical practice, how-ever, many patients fail to respond to conventional treatments. An evolving understanding of molecu-lar mechanisms underlying autoimmune haematologic disorders has facilitated the development of novel therapies, including Bruton's Tyrosine Kinase (BTK) inhibitors. BTK is fundamental in B-cell survival, and its inhibition has been used in a wide range of autoimmune and inflammatory conditions, as well as mature B cell malignancies. This paper reviews the role of BTK in immunity, evolution of BTK inhibitors, and the emerging evidence for BTK inhibitors in autoimmune haematologic conditions, primarily immune thrombocytopenia (ITP), and potential future clinical applications.(c) 2022 Elsevier Inc. All rights reserved.
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