Medical School, Federal University of Fronteira Sul, Chapecó, SC, Brazil.
Department of Biochemistry and Molecular Biology, Federal University of Santa Maria, Santa Maria, RS, Brazil.
J Immunol Res. 2020 Dec 1;2020:8632048. doi: 10.1155/2020/8632048. eCollection 2020.
Novel coronavirus disease 2019 (COVID-19) causes pulmonary and cardiovascular disorders and has become a worldwide emergency. Myocardial injury can be caused by direct or indirect damage, particularly mediated by a cytokine storm, a disordered immune response that can cause myocarditis, abnormal coagulation, arrhythmia, acute coronary syndrome, and myocardial infarction. The present review focuses on the mechanisms of this viral infection, cardiac biomarkers, consequences, and the possible therapeutic role of purinergic and adenosinergic signalling systems. In particular, we focus on the interaction of the extracellular nucleotide adenosine triphosphate (ATP) with its receptors P2X1, P2X4, P2X7, P2Y1, and P2Y2 and of adenosine (Ado) with A2A and A3 receptors, as well as their roles in host immune responses. We suggest that receptors of purinergic signalling could be ideal candidates for pharmacological targeting to protect against myocardial injury caused by a cytokine storm in COVID-19, in order to reduce systemic inflammatory damage to cells and tissues, preventing the progression of the disease by modulating the immune response and improving patient quality of life.
新型冠状病毒病 2019(COVID-19)可引起肺部和心血管疾病,已成为全球性紧急事件。心肌损伤可由直接或间接损伤引起,特别是由细胞因子风暴介导,这种免疫反应紊乱可导致心肌炎、异常凝血、心律失常、急性冠状动脉综合征和心肌梗死。本综述重点讨论了这种病毒感染的机制、心脏生物标志物、后果以及嘌呤能和腺苷能信号系统的可能治疗作用。特别是,我们专注于细胞外核苷酸三磷酸腺苷(ATP)与其受体 P2X1、P2X4、P2X7、P2Y1 和 P2Y2 的相互作用,以及腺苷(Ado)与 A2A 和 A3 受体的相互作用,以及它们在宿主免疫反应中的作用。我们认为嘌呤能信号受体可能是针对细胞因子风暴引起的 COVID-19 心肌损伤进行药物靶向治疗的理想候选物,以减少全身炎症对细胞和组织的损害,通过调节免疫反应和提高患者生活质量来防止疾病进展。