Nie Jiali, Zhou Ling, Tian Weiwei, Liu Xiansheng, Yang Liping, Yang Xingcheng, Zhang Yicheng, Wei Shuang, Wang Dao Wen, Wei Jia
Division of Cardiology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hubei Key Laboratory of Genetics and Molecular Mechanisms of Cardiological Disorders, Wuhan, China.
Signal Transduct Target Ther. 2025 Apr 16;10(1):112. doi: 10.1038/s41392-025-02178-y.
Cytokine storm (CS) is a severe systemic inflammatory syndrome characterized by the excessive activation of immune cells and a significant increase in circulating levels of cytokines. This pathological process is implicated in the development of life-threatening conditions such as fulminant myocarditis (FM), acute respiratory distress syndrome (ARDS), primary or secondary hemophagocytic lymphohistiocytosis (HLH), cytokine release syndrome (CRS) associated with chimeric antigen receptor-modified T (CAR-T) therapy, and grade III to IV acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation. The significant involvement of the JAK-STAT pathway, Toll-like receptors, neutrophil extracellular traps, NLRP3 inflammasome, and other signaling pathways has been recognized in the pathogenesis of CS. Therapies targeting these pathways have been developed or are currently being investigated. While novel drugs have demonstrated promising therapeutic efficacy in mitigating CS, the overall mortality rate of CS resulting from underlying diseases remains high. In the clinical setting, the management of CS typically necessitates a multidisciplinary team strategy encompassing the removal of abnormal inflammatory or immune system activation, the preservation of vital organ function, the treatment of the underlying disease, and the provision of life supportive therapy. This review provides a comprehensive overview of the key signaling pathways and associated cytokines implicated in CS, elucidates the impact of dysregulated immune cell activation, and delineates the resultant organ injury associated with CS. In addition, we offer insights and current literature on the management of CS in cases of FM, ARDS, systemic inflammatory response syndrome, treatment-induced CRS, HLH, and other related conditions.
细胞因子风暴(CS)是一种严重的全身性炎症综合征,其特征为免疫细胞过度激活以及循环细胞因子水平显著升高。这一病理过程与暴发性心肌炎(FM)、急性呼吸窘迫综合征(ARDS)、原发性或继发性噬血细胞性淋巴组织细胞增生症(HLH)、与嵌合抗原受体修饰T细胞(CAR-T)治疗相关的细胞因子释放综合征(CRS)以及异基因造血干细胞移植后的III至IV级急性移植物抗宿主病等危及生命的疾病的发生有关。JAK-STAT信号通路、Toll样受体、中性粒细胞胞外陷阱、NLRP3炎性小体及其他信号通路在CS的发病机制中具有重要作用。针对这些信号通路的治疗方法已被开发或正在研究中。虽然新型药物在减轻CS方面已显示出有前景的治疗效果,但由基础疾病导致的CS总体死亡率仍然很高。在临床环境中,CS的管理通常需要多学科团队策略,包括消除异常的炎症或免疫系统激活、维持重要器官功能、治疗基础疾病以及提供生命支持治疗。本综述全面概述了与CS相关的关键信号通路和细胞因子,阐明了免疫细胞激活失调的影响,并描述了与CS相关的器官损伤。此外,我们还提供了关于FM、ARDS、全身炎症反应综合征、治疗诱导的CRS、HLH及其他相关病症中CS管理的见解和当前文献。