Aphaia Pharma AG, Zug, Switzerland.
Department of Physiology, University of Toronto, Toronto, ON, Canada.
Front Endocrinol (Lausanne). 2020 Sep 30;11:583006. doi: 10.3389/fendo.2020.583006. eCollection 2020.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its clinical manifestation (COVID-19; coronavirus disease 2019) have caused a worldwide health crisis. Disruption of epithelial and endothelial barriers is a key clinical turning point that differentiates patients who are likely to develop severe COVID-19 outcomes: it marks a significant escalation in respiratory symptoms, loss of viral containment and a progression toward multi-organ dysfunction. These barrier mechanisms are independently compromised by known COVID-19 risk factors, including diabetes, obesity and aging: thus, a synergism between these underlying conditions and SARS-CoV-2 mechanisms may explain why these risk factors correlate with more severe outcomes. This review examines the key cellular mechanisms that SARS-CoV-2 and its underlying risk factors utilize to disrupt barrier function. As an outlook, we propose that glucagon-like peptide 1 (GLP-1) may be a therapeutic intervention that can slow COVID-19 progression and improve clinical outcome following SARS-CoV-2 infection. GLP-1 signaling activates barrier-promoting processes that directly oppose the pro-inflammatory mechanisms commandeered by SARS-CoV-2 and its underlying risk factors.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)及其临床表现(COVID-19;冠状病毒病 2019)已引发全球性健康危机。上皮和内皮屏障的破坏是区分可能发生严重 COVID-19 结局的患者的关键临床转折点:它标志着呼吸道症状显著加重、病毒失控以及向多器官功能障碍进展。这些屏障机制分别受到 COVID-19 已知风险因素的损害,包括糖尿病、肥胖症和衰老:因此,这些潜在条件和 SARS-CoV-2 机制之间的协同作用可能解释了为什么这些风险因素与更严重的结局相关。本综述检查了 SARS-CoV-2 及其潜在风险因素利用来破坏屏障功能的关键细胞机制。作为展望,我们提出胰高血糖素样肽 1(GLP-1)可能是一种治疗干预措施,可减缓 COVID-19 进展并改善 SARS-CoV-2 感染后的临床结局。GLP-1 信号激活促进屏障的过程,这些过程直接对抗 SARS-CoV-2 及其潜在风险因素所利用的促炎机制。