Massachusetts General Hospital, Mucosal Immunology and Biology Research Center, Boston, Massachusetts, USA.
Massachusetts General Hospital, Department of Pediatrics, Boston, Massachusetts, USA.
J Infect Dis. 2021 Dec 1;224(11):1821-1829. doi: 10.1093/infdis/jiab509.
Data on pediatric coronavirus disease 2019 (COVID-19) has lagged behind adults throughout the pandemic. An understanding of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral dynamics in children would enable data-driven public health guidance.
Respiratory swabs were collected from children with COVID-19. Viral load was quantified by reverse-transcription polymerase chain reaction (RT-PCR); viral culture was assessed by direct observation of cytopathic effects and semiquantitative viral titers. Correlations with age, symptom duration, and disease severity were analyzed. SARS-CoV-2 whole genome sequences were compared with contemporaneous sequences.
One hundred ten children with COVID-19 (median age, 10 years [range, 2 weeks-21 years]) were included in this study. Age did not impact SARS-CoV-2 viral load. Children were most infectious within the first 5 days of illness, and severe disease did not correlate with increased viral loads. Pediatric SARS-CoV-2 sequences were representative of those in the community and novel variants were identified.
Symptomatic and asymptomatic children can carry high quantities of live, replicating SARS-CoV-2, creating a potential reservoir for transmission and evolution of genetic variants. As guidance around social distancing and masking evolves following vaccine uptake in older populations, a clear understanding of SARS-CoV-2 infection dynamics in children is critical for rational development of public health policies and vaccination strategies to mitigate the impact of COVID-19.
在整个大流行期间,儿童 2019 年冠状病毒病(COVID-19)的数据落后于成年人。了解儿童中严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的病毒动力学将使数据驱动的公共卫生指导成为可能。
从 COVID-19 患儿中采集呼吸道拭子。通过逆转录聚合酶链反应(RT-PCR)定量病毒载量;通过直接观察细胞病变效应和半定量病毒滴度评估病毒培养。分析与年龄、症状持续时间和疾病严重程度的相关性。比较 SARS-CoV-2 全基因组序列与同期序列。
本研究共纳入 110 例 COVID-19 患儿(中位数年龄为 10 岁[范围,2 周-21 岁])。年龄对 SARS-CoV-2 病毒载量没有影响。患儿在发病的前 5 天最具传染性,严重疾病与病毒载量增加无关。儿科 SARS-CoV-2 序列代表了社区中的序列,并鉴定出了新的变异体。
有症状和无症状的儿童可携带大量活的、复制的 SARS-CoV-2,成为传播和遗传变异进化的潜在传染源。随着疫苗在老年人群中的接种,围绕社交距离和戴口罩的指导方针不断发展,因此,深入了解 SARS-CoV-2 在儿童中的感染动力学对于合理制定公共卫生政策和接种策略以减轻 COVID-19 的影响至关重要。