Department of Pathology, Microbiology, and Immunology, University of California, Davis, California; US Army Veterinary Corps, Washington, District of Columbia.
Department of Pathology, Microbiology, and Immunology, University of California, Davis, California.
Am J Pathol. 2023 Jun;193(6):690-701. doi: 10.1016/j.ajpath.2023.02.013. Epub 2023 Mar 10.
Clinical evidence of vascular dysfunction and hypercoagulability as well as pulmonary vascular damage and microthrombosis are frequently reported in severe cases of human coronavirus disease 2019 (COVID-19). Syrian golden hamsters recapitulate histopathologic pulmonary vascular lesions reported in patients with COVID-19. Herein, special staining techniques and transmission electron microscopy further define vascular pathologies in a Syrian golden hamster model of human COVID-19. The results show that regions of active pulmonary inflammation in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are characterized by ultrastructural evidence of endothelial damage with platelet marginalization and both perivascular and subendothelial macrophage infiltration. SARS-CoV-2 antigen/RNA was not detectable within affected blood vessels. Taken together, these findings suggest that the prominent microscopic vascular lesions in SARS-CoV-2-inoculated hamsters likely occur due to endothelial damage followed by platelet and macrophage infiltration.
临床证据表明,血管功能障碍和高凝状态以及肺血管损伤和微血栓形成在严重的 2019 年冠状病毒病(COVID-19)患者中经常出现。叙利亚金黄地鼠再现了 COVID-19 患者报告的组织病理学肺血管损伤。在此,特殊染色技术和透射电子显微镜进一步确定了人类 COVID-19 叙利亚金黄地鼠模型中的血管病理学。结果表明,在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的活跃肺部炎症区域,存在内皮损伤的超微结构证据,表现为血小板边缘化以及血管周围和血管下巨噬细胞浸润。在受影响的血管内未检测到 SARS-CoV-2 抗原/RNA。总之,这些发现表明,SARS-CoV-2 感染的仓鼠中突出的微观血管病变可能是由于内皮损伤,随后血小板和巨噬细胞浸润所致。