MMWR Morb Mortal Wkly Rep. 2021 May 14;70(19):712-716. doi: 10.15585/mmwr.mm7019e1.
Recent studies have documented the emergence and rapid growth of B.1.526, a novel variant of interest (VOI) of SARS-CoV-2, the virus that causes COVID-19, in the New York City (NYC) area after its identification in NYC in November 2020 (1-3). Two predominant subclades within the B.1.526 lineage have been identified, one containing the E484K mutation in the receptor-binding domain (1,2), which attenuates in vitro neutralization by multiple SARS-CoV-2 antibodies and is present in variants of concern (VOCs) first identified in South Africa (B.1.351) (4) and Brazil (P.1).* The NYC Department of Health and Mental Hygiene (DOHMH) analyzed laboratory and epidemiologic data to characterize cases of B.1.526 infection, including illness severity, transmission to close contacts, rates of possible reinfection, and laboratory-diagnosed breakthrough infections among vaccinated persons. Preliminary data suggest that the B.1.526 variant does not lead to more severe disease and is not associated with increased risk for infection after vaccination (breakthrough infection) or reinfection. Because relatively few specimens were sequenced over the study period, the statistical power might have been insufficient to detect modest differences in rates of uncommon outcomes such as breakthrough infection or reinfection. Collection of timely viral genomic data for a larger proportion of citywide cases and rapid integration with population-based surveillance data would enable improved understanding of the impact of emerging SARS-CoV-2 variants and specific mutations to help guide public health intervention efforts.
最近的研究记录了 B.1.526 的出现和快速增长,B.1.526 是导致 COVID-19 的 SARS-CoV-2 病毒的一种新型感兴趣变体 (VOI),这种变体于 2020 年 11 月在纽约市 (NYC) 被发现后在纽约市地区出现(1-3)。B.1.526 谱系内已经确定了两个主要的亚系,一个含有受体结合域中的 E484K 突变(1,2),这会削弱多种 SARS-CoV-2 抗体的体外中和作用,并且存在于南非(B.1.351)(4)和巴西(P.1)首次发现的关注变体 (VOC) 中。纽约市卫生局 (DOHMH) 分析了实验室和流行病学数据,以描述 B.1.526 感染病例,包括疾病严重程度、向密切接触者的传播、可能再次感染的比率,以及接种疫苗者的实验室诊断突破感染。初步数据表明,B.1.526 变体不会导致更严重的疾病,并且与接种疫苗后的感染(突破感染)或再次感染风险增加无关(突破感染)。由于研究期间测序的标本相对较少,因此在检测不太常见的结果(如突破感染或再次感染)的比率方面,统计能力可能不足。及时收集全市范围内更大比例病例的病毒基因组数据,并与基于人群的监测数据快速整合,将有助于更好地了解新兴 SARS-CoV-2 变体和特定突变的影响,以帮助指导公共卫生干预措施。