Laboratory of Molecular and Translational Human Infectious Diseases Research, Houston Methodist Hospital, Houston, Texas; Laboratory of Antibody Discovery and Accelerated Protein Therapeutics, Center for Infectious Diseases, Houston Methodist Research Institute and Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
Laboratory of Molecular and Translational Human Infectious Diseases Research, Houston Methodist Hospital, Houston, Texas.
Am J Pathol. 2022 Apr;192(4):642-652. doi: 10.1016/j.ajpath.2022.01.007. Epub 2022 Feb 3.
Genetic variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to dramatically alter the landscape of the coronavirus disease 2019 (COVID-19) pandemic. The recently described variant of concern designated Omicron (B.1.1.529) has rapidly spread worldwide and is now responsible for the majority of COVID-19 cases in many countries. Because Omicron was recognized recently, many knowledge gaps exist about its epidemiology, clinical severity, and disease course. A genome sequencing study of SARS-CoV-2 in the Houston Methodist health care system identified 4468 symptomatic patients with infections caused by Omicron from late November 2021 through January 5, 2022. Omicron rapidly increased in only 3 weeks to cause 90% of all new COVID-19 cases, and at the end of the study period caused 98% of new cases. Compared with patients infected with either Alpha or Delta variants in our health care system, Omicron patients were significantly younger, had significantly increased vaccine breakthrough rates, and were significantly less likely to be hospitalized. Omicron patients required less intense respiratory support and had a shorter length of hospital stay, consistent with on average decreased disease severity. Two patients with Omicron stealth sublineage BA.2 also were identified. The data document the unusually rapid spread and increased occurrence of COVID-19 caused by the Omicron variant in metropolitan Houston, Texas, and address the lack of information about disease character among US patients.
严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 的遗传变异继续显著改变 2019 年冠状病毒病 (COVID-19) 大流行的格局。最近描述的关切变异株被指定为奥密克戎 (B.1.1.529),已迅速在全球范围内传播,目前是许多国家 COVID-19 病例的主要原因。由于奥密克戎最近才被发现,因此其流行病学、临床严重程度和疾病过程存在许多知识空白。休斯顿卫理公会医疗保健系统对 SARS-CoV-2 的基因组测序研究确定了 4468 名有症状的患者,他们的感染是由 2021 年 11 月下旬至 2022 年 1 月 5 日期间的奥密克戎引起的。奥密克戎仅在 3 周内迅速增加,导致 90%的新 COVID-19 病例,在研究期末导致 98%的新病例。与我们医疗系统中感染 Alpha 或 Delta 变异株的患者相比,奥密克戎患者明显更年轻,疫苗突破性感染率明显更高,住院的可能性明显更低。奥密克戎患者需要的呼吸支持强度较低,住院时间较短,与疾病严重程度平均降低一致。还发现了两名感染奥密克戎 stealth 亚系 BA.2 的患者。这些数据记录了奥密克戎变异株在德克萨斯州休斯顿大都市地区异常迅速传播和 COVID-19 发病率增加的情况,并解决了美国患者中关于疾病特征的信息不足的问题。