Role of the IL-2 inducible tyrosine kinase ITK and its inhibitors in disease pathogenesis

被引:36
|
作者
Lechner, Kristina S. [1 ]
Neurath, Markus F. [1 ,2 ,3 ]
Weigmann, Benno [1 ,4 ]
机构
[1] Univ Erlangen Nurnberg, Kussmaul Campus Med Res, Dept Med 1, Hartmannstr 14, D-91052 Erlangen, Germany
[2] Deutsch Zentrum Immuntherapie DZI, Ulmenweg 18, D-91054 Erlangen, Germany
[3] Ludwig Demling Endoscopy Ctr Excellence, Ulmenweg 18, D-91054 Erlangen, Germany
[4] Friedrich Alexander Univ Erlangen Nurnberg, Med Immunol Campus Erlangen, Med Clin 1, D-91052 Erlangen, Germany
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2020年 / 98卷 / 10期
关键词
ITK; Autoimmune diseases; Cancer; Inhibitor; T-CELL KINASE; TEC FAMILY KINASES; MICE LACKING; CYTOKINE PRODUCTION; ALLERGIC-ASTHMA; MOUSE MODELS; RECEPTOR; ACTIVATION; LYMPHOMA; RLK;
D O I
10.1007/s00109-020-01958-z
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ITK (IL-2-inducible tyrosine kinase) belongs to the Tec family kinases and is mainly expressed in T cells. It is involved in TCR signalling events driving processes like T cell development as well as Th2, Th9 and Th17 responses thereby controlling the expression of pro-inflammatory cytokines. Studies have shown that ITK is involved in the pathogenesis of autoimmune diseases as well as in carcinogenesis. The loss of ITK or its activity either by mutation or by the use of inhibitors led to a beneficial outcome in experimental models of asthma, inflammatory bowel disease and multiple sclerosis among others. In humans, biallelic mutations in the ITK gene locus result in a monogenetic disorder leading to T cell dysfunction; in consequence, mainly EBV infections can lead to severe immune dysregulation evident by lymphoproliferation, lymphoma and hemophagocytic lymphohistiocytosis. Furthermore, patients who suffer from angioimmunoblastic T cell lymphoma have been found to express significantly more ITK. These findings put ITK in the strong focus as a target for drug development.
引用
收藏
页码:1385 / 1395
页数:11
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