JAK/STAT通路在T细胞淋巴瘤发病机制中的紊乱:免疫治疗的意义。

IF 26.9 1区 医学 Q1 IMMUNOLOGY
T. Waldmann, Jing Chen
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引用次数: 114

摘要

常见的γ受体依赖性细胞因子及其JAK/STAT途径在T细胞免疫中起着关键作用。该系统的异常激活在通过pSTAT3/pSTAT5磷酸化评估的各种T细胞恶性肿瘤中普遍存在。激活突变在一些但不是所有的病例中都有描述。JAK1和STAT3对于这些T细胞系的增殖和存活是必需的,无论JAK或STAT是否突变。激活JAK和STAT突变不足以启动白血病细胞增殖,而只能增强细胞因子途径上游的信号。激活需要完整的途径,包括细胞因子受体作为所需下游JAK/STAT蛋白的支架和对接位点。JAK激酶抑制剂抑制了白血病T细胞系的增殖。JAK/STAT系统激活在T细胞恶性肿瘤中普遍存在,这一发现表明了新的治疗方法,包括常见γ细胞因子的抗体、细胞因子受体相互作用的抑制剂和JAK激酶抑制剂,这些抑制剂可能会彻底改变T细胞恶性病的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disorders of the JAK/STAT Pathway in T Cell Lymphoma Pathogenesis: Implications for Immunotherapy.
Common gamma receptor-dependent cytokines and their JAK/STAT pathways play pivotal roles in T cell immunity. Abnormal activation of this system was pervasive in diverse T cell malignancies assessed by pSTAT3/pSTAT5 phosphorylation. Activating mutations were described in some but not all cases. JAK1 and STAT3 were required for proliferation and survival of these T cell lines whether or not JAKs or STATs were mutated. Activating JAK and STAT mutations were not sufficient to initiate leukemic cell proliferation but rather only augmented signals from upstream in the cytokine pathway. Activation required the full pathway, including cytokine receptors acting as scaffolds and docking sites for required downstream JAK/STAT proteins. JAK kinase inhibitors have depressed leukemic T cell line proliferation. The insight that JAK/STAT system activation is pervasive in T cell malignancies suggests novel therapeutic approaches that include antibodies to common gamma cytokines, inhibitors of cytokine-receptor interactions, and JAK kinase inhibitors that may revolutionize therapy for T cell malignancies.
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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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