Pharmacology Department, College of Medicine, Minia University, Minya, Egypt.
Inflammopharmacology. 2022 Feb;30(1):343-348. doi: 10.1007/s10787-021-00896-7. Epub 2021 Nov 25.
We have previously published several papers illustrating numerous immunomodulatory and anti-inflammatory potential benefits when we repurposed safe, generic non-steroidal anti-inflammatory drugs (NSAIDs)/nitazoxanide/azithromycin (Kelleni's protocol), to early manage our COVID-19 pediatric, adult, and pregnant patients. In this manuscript, we discuss some recently published meta-analysis and clinical studies supporting our practice and discuss a molecular study that might be interpreted as an academic proof that our protocol might also prevent SARS-CoV-2 replication. Moreover, after aspirin has been suggested to be independently associated with reduced risk of mechanical ventilation, ICU admission and in-hospital mortality of COVID-19, we claim that the molecular interpretation of the results that led to this suggestion was not scientifically accurate, and we provide our academic interpretation confirming that low-dose aspirin is least likely to improve COVID-19 mortality through anticoagulation as was suggested. Furthermore, we describe other potential benefits related to aspirin-triggered lipoxins and resolvins while illustrating how NSAIDs interfere with COX-1, COX-2, SARS-CoV-2/ SARS-CoV-2 ORF protein-dependent activation of caspases and their subsequent mitochondrial dysfunction, endoplasmic reticulum stress, apoptosis and necroptosis which were associated with COVID-19 complications. Similarly, NSAIDs are known caspase inhibitors and thus they might independently inhibit other caspase-related COVID-19-associated downstream pathological signaling mechanisms. Finally, we postulated that CARD-14, a caspase recruitment domain-containing protein, polymorphisms might play a role in the development of severe and critical COVID-19 and confirmed our old call to early adopt NSAIDs, as an integral part of Kelleni's protocol, as of choice in its management aiming to end this pandemic.
我们之前发表了几篇论文,说明了重新利用安全、通用的非甾体抗炎药(NSAIDs)/硝唑尼特/阿奇霉素(Kelleni 方案)对我们的 COVID-19 儿科、成人和孕妇患者进行早期管理时具有许多免疫调节和抗炎的潜在益处。在本文中,我们讨论了一些最近发表的荟萃分析和临床研究,这些研究支持我们的实践,并讨论了一项分子研究,该研究可以被解释为学术证据,表明我们的方案也可能阻止 SARS-CoV-2 复制。此外,在阿司匹林被认为与 COVID-19 患者机械通气、入住 ICU 和院内死亡率降低独立相关后,我们声称导致这一建议的结果的分子解释在科学上并不准确,我们提供了我们的学术解释,证实低剂量阿司匹林不太可能通过抗凝作用改善 COVID-19 的死亡率,正如所建议的那样。此外,我们描述了与阿司匹林触发的脂氧素和 resolvins 相关的其他潜在益处,同时说明了 NSAIDs 如何干扰 COX-1、COX-2、SARS-CoV-2/SARS-CoV-2 ORF 蛋白依赖性 caspase 激活及其随后的线粒体功能障碍、内质网应激、细胞凋亡和 necroptosis,这些都与 COVID-19 并发症有关。同样,NSAIDs 是已知的 caspase 抑制剂,因此它们可能独立抑制其他与 caspase 相关的 COVID-19 相关下游病理信号机制。最后,我们假设 caspase 募集结构域蛋白 CARD-14 的多态性可能在严重和危重症 COVID-19 的发展中起作用,并证实了我们早期采用 NSAIDs 的旧呼吁,将其作为 Kelleni 方案的一个组成部分,作为其管理的首选,旨在结束这一大流行。