鲁索利替尼
贾纳斯激酶
医学
骨髓纤维化
酪氨酸激酶2
JAK-STAT信号通路
Janus激酶1
移植物抗宿主病
细胞因子
Janus激酶2
托法替尼
免疫学
癌症研究
药理学
肿瘤科
移植
内科学
酪氨酸激酶
骨髓
受体
生长因子
类风湿性关节炎
血小板源性生长因子受体
作者
Annalisa Marcuzzi,Erika Rimondi,Elisabetta Melloni,Arianna Gonelli,A. Grasso,Egidio Barbi,Natalia Maximova
摘要
Janus kinases (JAK) are a family of tyrosine kinases (JAK1, JAK2, JAK3, and TYK2) that transduce cytokine-mediated signals through the JAK-STAT metabolic pathway. These kinases act by regulating the transcription of specific genes capable of inducing biological responses in several immune cell subsets. Inhibition of Janus kinases interferes with the JAK-STAT signaling pathway. Besides being used in the treatment of cancer and inflammatory diseases, in recent years, they have also been used to treat inflammatory conditions, such as graft-versus-host disease (GVHD) and cytokine release syndrome as complications of allogeneic hematopoietic stem cell transplantation and cell therapy. Recently, the FDA approved the use of ruxolitinib, a JAK1/2 inhibitor, in the treatment of acute steroid-refractory GVHD (SR-aGVHD), highlighting the role of JAK inhibition in this immune deregulation. Ruxolitinib was initially used to treat myelofibrosis and true polycythemia in a high-dose treatment and caused hematological toxicity. Since a lower dosage often could not be effective, the use of ruxolitinib was suspended. Subsequently, ruxolitinib was evaluated in adult patients with SR-aGVHD and was found to achieve a rapid and effective response. In addition, its early low-dose use in pediatric patients affected by GVHD has proved effective, safe, and reasonably preventive. The review aims to describe the potential properties of ruxolitinib to identify new therapeutic strategies.
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