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

被引:0
|
作者
Kristina S. Lechner
Markus F. Neurath
Benno Weigmann
机构
[1] University of Erlangen-Nürnberg,Department of Medicine 1, Kussmaul Campus for Medical Research
[2] Deutsches Zentrum Immuntherapie (DZI),Medical Immunology Campus Erlangen, Medical Clinic 1
[3] Ludwig Demling Endoscopy Center of Excellence,undefined
[4] Friedrich-Alexander University Erlangen-Nürnberg,undefined
来源
关键词
ITK; Autoimmune diseases; Cancer; Inhibitor;
D O I
暂无
中图分类号
学科分类号
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:10
相关论文
共 50 条
  • [31] INHIBITION OF INTERLEUKIN-2 (IL-2)-STIMULATED TYROSINE KINASE-ACTIVITY BY LEFLUNOMIDE
    NIKCEVICH, DA
    FINNEGAN, A
    CHONG, ASF
    WILLIAMS, JW
    BREMER, EG
    AGENTS AND ACTIONS, 1994, 41 : C279 - C282
  • [32] IL-2 BINDING ACTIVATES A TYROSINE-PHOSPHORYLATED PHOSPHATIDYLINOSITOL-3-KINASE
    MERIDA, I
    DIEZ, E
    GAULTON, GN
    JOURNAL OF IMMUNOLOGY, 1991, 147 (07): : 2202 - 2207
  • [33] A TYROSINE KINASE PHYSICALLY ASSOCIATES WITH THE BETA-SUBUNIT OF THE HUMAN IL-2 RECEPTOR
    FUNG, MR
    SCEARCE, RM
    HOFFMAN, JA
    PEFFER, NJ
    HAMMES, SR
    HOSKING, JB
    SCHMANDT, R
    KUZIEL, WA
    HAYNES, BF
    MILLS, GB
    GREENE, WC
    JOURNAL OF IMMUNOLOGY, 1991, 147 (04): : 1253 - 1260
  • [34] Role of proline-rich tyrosine kinase 2 (Pyk2) in the pathogenesis of Alzheimer's disease
    Kumar, Rahul
    Tiwari, Vishvanath
    Dey, Sharmistha
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2022, 56 (09) : 5442 - 5452
  • [35] INTERLEUKIN-2 (IL-2) INDUCED TYROSINE KINASE-ACTIVITY AND GENE INDUCTION BY WILD-TYPE AND MUTANT IL-2 RECEPTORS
    WILLIAMSON, P
    MERIDA, I
    GAULTON, G
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, : 248 - 248
  • [36] Possible implication of IL-23-IL-17 axis and proline-rich tyrosine kinase 2 in pathogenesis of Kawasaki disease
    Suzuki, C.
    Nakamura, A.
    Okigaki, M.
    Ohno, N.
    Okamoto-Hamaoka, A.
    Yoshioka, A.
    Yahata, N.
    Ikeda, K.
    Hamaoka, K.
    EUROPEAN HEART JOURNAL, 2014, 35 : 581 - 581
  • [37] Selective tyrosine kinase 2 inhibitors in inflammatory bowel disease
    Nielsen, Ole Haagen
    Boye, Theresa Louise
    Chakravarti, Deepavali
    Gubatan, John
    TRENDS IN PHARMACOLOGICAL SCIENCES, 2022, 43 (05) : 424 - 436
  • [38] IL-2-INDUCED SIGNAL TRANSDUCTION - INVOLVEMENT OF TYROSINE KINASE AND IL-2 RECEPTOR GAMMA-CHAIN
    SUGAMURA, K
    TAKESHITA, T
    ASAO, H
    KUMAKI, S
    OHBO, K
    OHTANI, K
    NAKAMURA, M
    LYMPHOKINE RESEARCH, 1990, 9 (04): : 539 - 542
  • [39] The role of tyrosine kinase ITK in T cell activation signaling pathways in vivo
    Ragin, MJ
    MOLECULAR BIOLOGY OF THE CELL, 2002, 13 : 427A - 427A
  • [40] 2 REGIONS WITHIN THE HUMAN IL-2 GENE PROMOTER ARE IMPORTANT FOR INDUCIBLE IL-2 EXPRESSION
    WILLIAMS, TM
    EISENBERG, L
    BURLEIN, JE
    NORRIS, CA
    PANCER, S
    YAO, D
    BURGER, S
    KAMOUN, M
    KANT, JA
    JOURNAL OF IMMUNOLOGY, 1988, 141 (02): : 662 - 666