Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Jouf University, Sakaka, 72388, Saudi Arabia.
Northwestern Polytechnical University, Xian, 710060, China.
Mol Biol Rep. 2024 Aug 8;51(1):894. doi: 10.1007/s11033-024-09839-1.
Adenosine is a neuro- and immunomodulator that functions via G protein-coupled cell surface receptors. Several microbes, including viruses, use the adenosine signaling pathway to escape from host defense systems. Since the recent research developments in its role in health and disease, adenosine and its signaling pathway have attracted attention for targeting to treat many diseases. The therapeutic role of adenosine has been extensively studied for neurological, cardiovascular, and inflammatory disorders and bacterial pathophysiology, but published data on the role of adenosine in viral infections are lacking. Therefore, the purpose of this review article was to explain in detail the therapeutic role of adenosine signaling against viral infections, particularly COVID-19 and HIV. Several therapeutic approaches targeting A2AR-mediated pathways are in development and have shown encouraging results in decreasing the intensity of inflammatory reaction. The hypoxia-adenosinergic mechanism provides protection from inflammation-mediated tissue injury during COVID-19. A2AR expression increased remarkably in CD39 + and CD8 + T cells harvested from HIV patients in comparison to healthy subjects. A combined in vitro treatment performed by blocking PD-1 and CD39/adenosine signaling produced a synergistic outcome in restoring the CD8 + T cells funstion in HIV patients. We suggest that A2AR is an ideal target for pharmacological interventions against viral infections because it reduces inflammation, prevents disease progression, and ultimately improves patient survival.
腺苷是一种神经和免疫调节剂,通过 G 蛋白偶联细胞表面受体发挥作用。包括病毒在内的几种微生物利用腺苷信号通路逃避宿主防御系统。由于其在健康和疾病中的作用的最新研究进展,腺苷及其信号通路已成为治疗许多疾病的靶点而受到关注。腺苷在神经、心血管和炎症性疾病以及细菌发病机制中的治疗作用已得到广泛研究,但关于其在病毒感染中的作用的已发表数据却很少。因此,本文的目的是详细解释腺苷信号在对抗病毒感染(特别是 COVID-19 和 HIV)中的治疗作用。几种针对 A2AR 介导途径的治疗方法正在开发中,并已显示出在降低炎症反应强度方面的令人鼓舞的结果。低氧-腺苷能机制为 COVID-19 期间炎症介导的组织损伤提供了保护。与健康受试者相比,从 HIV 患者中采集的 CD39+和 CD8+T 细胞中 A2AR 的表达显著增加。在体外联合阻断 PD-1 和 CD39/腺苷信号的处理在恢复 HIV 患者 CD8+T 细胞功能方面产生了协同作用。我们认为,A2AR 是针对病毒感染的药理学干预的理想靶点,因为它可以减轻炎症、阻止疾病进展,最终提高患者的生存率。