类风湿性关节炎
关节炎
激酶
医学
发病机制
免疫学
自身免疫性疾病
癌症研究
信号转导
酪氨酸激酶
受体
生物
细胞生物学
内科学
抗体
作者
Babita Madan,Kunli Goh,Stefan Hart,Anthony D. William,Ramesh Jayaraman,Kantharaj Ethirajulu,Brian Dymock,Jeanette M. Wood
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2012-10-15
卷期号:189 (8): 4123-4134
被引量:31
标识
DOI:10.4049/jimmunol.1200675
摘要
Abstract SB1578 is a novel, orally bioavailable JAK2 inhibitor with specificity for JAK2 within the JAK family and also potent activity against FLT3 and c-Fms. These three tyrosine kinases play a pivotal role in activation of pathways that underlie the pathogenesis of rheumatoid arthritis. SB1578 blocks the activation of these kinases and their downstream signaling in pertinent cells, leading to inhibition of pathological cellular responses. The biochemical and cellular activities of SB1578 translate into its high efficacy in two rodent models of arthritis. SB1578 not only prevents the onset of arthritis but is also potent in treating established disease in collagen-induced arthritis mice with beneficial effects on histopathological parameters of bone resorption and cartilage damage. SB1578 abrogates the inflammatory response and prevents the infiltration of macrophages and neutrophils into affected joints. It also leads to inhibition of Ag-presenting dendritic cells and inhibits the autoimmune component of the disease. In summary, SB1578 has a unique kinase spectrum, and its pharmacological profile provides a strong rationale for the ongoing clinical development in autoimmune diseases.
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