School of Human Sciences, London Metropolitan University, U.K.
Biosciences Research Group, School of Life and Medical Sciences, University of Hertfordshire, U.K.
Clin Sci (Lond). 2022 Oct 28;136(20):1439-1447. doi: 10.1042/CS20220638.
This perspective considers the benefits of the potential future use of the cell permeant calpain inhibitor, calpeptin, as a drug to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Recent work has reported calpeptin's capacity to inhibit entry of the virus into cells. Elsewhere, several drugs, including calpeptin, were found to be able to inhibit extracellular vesicle (EV) biogenesis. Unsurprisingly, because of similarities between viral and EV release mechanisms, calpeptin has also been shown to inhibit viral egress. This approach, identifying calpeptin, through large-scale screening studies as a candidate drug to treat COVID-19, however, has not considered the longer term likely benefits of calpain inhibition, post-COVID-19. This perspective will reflect on the capacity of calpeptin for treating long COVID by inhibiting the overproduction of neutrophil extracellular traps potentially damaging lung cells and promoting clotting, together with limiting associated chronic inflammation, tissue damage and pulmonary fibrosis. It will also reflect on the tolerated and detrimental in vivo side-effects of calpain inhibition from various preclinical studies.
本文从潜在的未来用途的角度出发,考虑了细胞透性钙蛋白酶抑制剂 calpeptin 在治疗严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染方面的应用。最近的研究报告表明 calpeptin 能够抑制病毒进入细胞。此外,包括 calpeptin 在内的几种药物已被发现能够抑制细胞外囊泡(EV)的生物发生。由于病毒释放机制与 EV 释放机制相似,因此 calpeptin 也被证明能够抑制病毒的出芽。然而,这种通过大规模筛选研究将 calpeptin 确定为治疗 COVID-19 的候选药物的方法,并未考虑 calpain 抑制在后 COVID-19 时期的长期潜在益处。本文将通过抑制可能损害肺细胞并促进凝血的中性粒细胞胞外陷阱的过度产生,以及限制相关的慢性炎症、组织损伤和肺纤维化,来反映 calpeptin 治疗长 COVID 的潜力。本文还将反映从各种临床前研究中 calpain 抑制的可耐受和有害的体内副作用。