SARS-CoV-2感染患者肠道异常:组织病理学变化反映疾病机制

Rhonda K Yantiss, LiHui Qin, Bing He, Carl V Crawford, Surya Seshan, Sanjay Patel, Nabeel Wahid, Jose Jessurun
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引用次数: 17

摘要

大约20%的有症状的与综合征相关的冠状病毒-2 (SARS-CoV-2)感染患者出现胃肠道出血和/或腹泻。大多数管理没有内窥镜评估,因为从业者感染的风险超过了活检分析的价值,除非症状危及生命。因此,关于2019冠状病毒病(COVID-19)胃肠道表现的大部分已知信息都是从遭受广泛缺血性损伤和/或保存不良的手术和尸检病例中收集的。尽管全球有超过300万人死于COVID-19,但没有详细的报告描述SARS-CoV-2的任何其他胃肠道影响。本研究的目的是通过一个小病例系列报告与SARS-CoV-2感染相关的肠道发现,其中包括1例直接病毒细胞病变证据和2例归因于病毒感染的继发性损伤。感染可通过针对SARS-CoV-2刺突蛋白的免疫组织化学染色、刺突蛋白编码RNA的原位杂交和上皮内病毒的超微结构可视化来证实。它诱导细胞质泡和簇状上皮细胞而不引起炎症,可能不会引起症状。相比之下,SARS-CoV-2感染可在不再检测到病毒后引起胃肠道症状,这反映了全身细胞因子和补体级联的激活,而不是直接的病毒损伤。可逆性粘膜缺血以微血管损伤为特征,包括出血、小血管血栓和富血小板血栓。系统性细胞因子的细化和生态失调可能解释了伴随腹泻症状的上皮细胞损伤。这些观察结果与临床和体外数据一致,有助于我们了解COVID-19的多种表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intestinal Abnormalities in Patients With SARS-CoV-2 Infection: Histopathologic Changes Reflect Mechanisms of Disease.

Approximately 20% of patients with symptomatic syndrome-associated coronavirus-2 (SARS-CoV-2) infection have gastrointestinal bleeding and/or diarrhea. Most are managed without endoscopic evaluation because the risk of practitioner infection outweighs the value of biopsy analysis unless symptoms are life-threatening. As a result, much of what is known about the gastrointestinal manifestations of coronavirus disease-2019 (COVID-19) has been gleaned from surgical and autopsy cases that suffer from extensive ischemic injury and/or poor preservation. There are no detailed reports describing any other gastrointestinal effects of SARS-CoV-2 even though >3,000,000 people have died from COVID-19 worldwide. The purpose of this study is to report the intestinal findings related to SARS-CoV-2 infection by way of a small case series including one with evidence of direct viral cytopathic effect and 2 with secondary injury attributed to viral infection. Infection can be confirmed by immunohistochemical stains directed against SARS-CoV-2 spike protein, in situ hybridization for spike protein-encoding RNA, and ultrastructural visualization of viruses within the epithelium. It induces cytoplasmic blebs and tufted epithelial cells without inflammation and may not cause symptoms. In contrast, SARS-CoV-2 infection can cause gastrointestinal symptoms after the virus is no longer detected, reflecting systemic activation of cytokine and complement cascades rather than direct viral injury. Reversible mucosal ischemia features microvascular injury with hemorrhage, small vessel thrombosis, and platelet-rich thrombi. Systemic cytokine elaboration and dysbiosis likely explain epithelial cell injury that accompanies diarrheal symptoms. These observations are consistent with clinical and in vitro data and contribute to our understanding of the protean manifestations of COVID-19.

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