Department of Brain Sciences, Imperial College London, Hammersmith Hospital, London, UK.
Department of Cellular Pathology, Northwest London Pathology, Charing Cross Hospital Campus, London, UK.
J Pathol. 2022 Jun;257(2):198-217. doi: 10.1002/path.5878. Epub 2022 Mar 31.
SARS-CoV-2, the causative agent of COVID-19, typically manifests as a respiratory illness, although extrapulmonary involvement, such as in the gastrointestinal tract and nervous system, as well as frequent thrombotic events, are increasingly recognised. How this maps onto SARS-CoV-2 organ tropism at the histological level, however, remains unclear. Here, we perform a comprehensive validation of a monoclonal antibody against the SARS-CoV-2 nucleocapsid protein (NP) followed by systematic multisystem organ immunohistochemistry analysis of the viral cellular tropism in tissue from 36 patients, 16 postmortem cases and 16 biopsies with polymerase chain reaction (PCR)-confirmed SARS-CoV-2 status from the peaks of the pandemic in 2020 and four pre-COVID postmortem controls. SARS-CoV-2 anti-NP staining in the postmortem cases revealed broad multiorgan involvement of the respiratory, digestive, haematopoietic, genitourinary and nervous systems, with a typical pattern of staining characterised by punctate paranuclear and apical cytoplasmic labelling. The average time from symptom onset to time of death was shorter in positively versus negatively stained postmortem cases (mean = 10.3 days versus mean = 20.3 days, p = 0.0416, with no cases showing definitive staining if the interval exceeded 15 days). One striking finding was the widespread presence of SARS-CoV-2 NP in neurons of the myenteric plexus, a site of high ACE2 expression, the entry receptor for SARS-CoV-2, and one of the earliest affected cells in Parkinson's disease. In the bone marrow, we observed viral SARS-CoV-2 NP within megakaryocytes, key cells in platelet production and thrombus formation. In 15 tracheal biopsies performed in patients requiring ventilation, there was a near complete concordance between immunohistochemistry and PCR swab results. Going forward, our findings have relevance to correlating clinical symptoms with the organ tropism of SARS-CoV-2 in contemporary cases as well as providing insights into potential long-term complications of COVID-19. © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
SARS-CoV-2,即导致 COVID-19 的病原体,通常表现为呼吸道疾病,尽管越来越多的人认识到其涉及肺外器官,如胃肠道和神经系统,以及频繁发生血栓事件。然而,这种情况在组织学水平上如何映射到 SARS-CoV-2 的器官嗜性仍不清楚。在这里,我们对一种针对 SARS-CoV-2 核衣壳蛋白(NP)的单克隆抗体进行了全面验证,随后对 2020 年大流行高峰期的 36 名患者、16 名尸检病例和 16 名聚合酶链反应(PCR)确诊的 SARS-CoV-2 活检组织中的病毒细胞嗜性进行了系统的多系统器官免疫组织化学分析,以及 4 名 COVID-19 前尸检对照。尸检病例中的 SARS-CoV-2 抗 NP 染色显示呼吸道、消化、造血、泌尿生殖和神经系统广泛受累,具有典型的染色模式,特征为点状核旁和顶细胞质标记。与染色阴性的尸检病例相比,症状发作到死亡的平均时间在染色阳性的尸检病例中更短(平均值=10.3 天与平均值=20.3 天,p=0.0416,如果间隔超过 15 天,则没有病例显示明确的染色)。一个引人注目的发现是 SARS-CoV-2 NP 在肌间神经丛神经元中的广泛存在,肌间神经丛是 ACE2 高表达的部位,也是 SARS-CoV-2 的进入受体,也是帕金森病最早受影响的细胞之一。在骨髓中,我们观察到巨核细胞内存在病毒 SARS-CoV-2 NP,巨核细胞是血小板生成和血栓形成的关键细胞。在需要通气的 15 名气管活检患者中,免疫组织化学和 PCR 拭子结果几乎完全一致。展望未来,我们的研究结果与将临床症状与当代 SARS-CoV-2 的器官嗜性相关联以及提供 COVID-19 潜在长期并发症的见解有关。