Klein Klara, Stoiber Dagmar, Sexl Veronika, Witalisz-Siepracka Agnieszka
Department of Biomedical Science, Institute of Pharmacology and Toxicology, University of Veterinary Medicine Vienna, 1210 Vienna, Austria.
Department of Pharmacology, Physiology and Microbiology, Division Pharmacology, Karl Landsteiner University of Health Sciences, 3500 Krems, Austria.
Cancers (Basel). 2021 May 26;13(11):2611. doi: 10.3390/cancers13112611.
The Janus kinase-signal transducer and activator of transcription (JAK-STAT) pathway propagates signals from a variety of cytokines, contributing to cellular responses in health and disease. Gain of function mutations in JAKs or STATs are associated with malignancies, with being the main driver mutation in myeloproliferative neoplasms (MPN). Therefore, inhibition of this pathway is an attractive therapeutic strategy for different types of cancer. Numerous JAK inhibitors (JAKinibs) have entered clinical trials, including the JAK1/2 inhibitor Ruxolitinib approved for the treatment of MPN. Importantly, loss of function mutations in JAK-STAT members are a cause of immune suppression or deficiencies. MPN patients undergoing Ruxolitinib treatment are more susceptible to infections and secondary malignancies. This highlights the suppressive effects of JAKinibs on immune responses, which renders them successful in the treatment of autoimmune diseases but potentially detrimental for cancer patients. Here, we review the current knowledge on the effects of JAKinibs on immune cells in the context of hematological malignancies. Furthermore, we discuss the potential use of JAKinibs for the treatment of diseases in which lymphocytes are the source of malignancies. In summary, this review underlines the necessity of a robust immune profiling to provide the best benefit for JAKinib-treated patients.
Janus激酶-信号转导子和转录激活子(JAK-STAT)通路传递来自多种细胞因子的信号,在健康和疾病状态下促成细胞反应。JAK或STAT的功能获得性突变与恶性肿瘤相关,其中JAK2是骨髓增殖性肿瘤(MPN)的主要驱动突变。因此,抑制该通路是针对不同类型癌症的一种有吸引力的治疗策略。众多JAK抑制剂(JAKinibs)已进入临床试验,包括被批准用于治疗MPN的JAK1/2抑制剂鲁索替尼。重要的是,JAK-STAT成员的功能丧失性突变是免疫抑制或免疫缺陷的一个原因。接受鲁索替尼治疗的MPN患者更容易发生感染和继发性恶性肿瘤。这凸显了JAKinibs对免疫反应的抑制作用,这使得它们在治疗自身免疫性疾病方面取得成功,但对癌症患者可能有害。在此,我们综述了目前关于JAKinibs在血液系统恶性肿瘤背景下对免疫细胞影响的知识。此外,我们讨论了JAKinibs在治疗淋巴细胞是恶性肿瘤来源的疾病中的潜在用途。总之,本综述强调了进行全面免疫分析以为接受JAKinib治疗的患者提供最大益处的必要性。