Department of Microbiology and Immunology, Uniformed Services University of the Health Science, Bethesda, MD, USA.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc, Bethesda, MD, USA.
BMC Infect Dis. 2021 Jun 9;21(1):544. doi: 10.1186/s12879-021-06233-1.
SARS-CoV-2 is a recently emerged pandemic coronavirus (CoV) capable of causing severe respiratory illness. However, a significant number of infected people present as asymptomatic or pauci-symptomatic. In this prospective assessment of at-risk healthcare workers (HCWs) we seek to determine whether pre-existing antibody or T cell responses to previous seasonal human coronavirus (HCoV) infections affect immunological or clinical responses to SARS-CoV-2 infection or vaccination.
A cohort of 300 healthcare workers, confirmed negative for SARS-CoV-2 exposure upon study entry, will be followed for up to 1 year with monthly serology analysis of IgM and IgG antibodies against the spike proteins of SARS-CoV-2 and the four major seasonal human coronavirus - HCoV-OC43, HCoV-HKU1, HCoV-229E, and HCoV-NL63. Participants will complete monthly questionnaires that ask about Coronavirus Disease 2019 (COVID-19) exposure risks, and a standardized, validated symptom questionnaire (scoring viral respiratory disease symptoms, intensity and severity) at least twice monthly and any day when any symptoms manifest. SARS-CoV-2 PCR testing will be performed any time participants develop symptoms consistent with COVID-19. For those individuals that seroconvert and/or test positive by SARS-CoV-2 PCR, or receive the SARS-CoV-2 vaccine, additional studies of T cell activation and cytokine production in response to SARS-CoV-2 peptide pools and analysis of Natural Killer cell numbers and function will be conducted on that participant's cryopreserved baseline peripheral blood mononuclear cells (PBMCs). Following the first year of this study we will further analyze those participants having tested positive for COVID-19, and/or having received an authorized/licensed SARS-CoV-2 vaccine, quarterly (year 2) and semi-annually (years 3 and 4) to investigate immune response longevity.
This study will determine the frequency of asymptomatic and pauci-symptomatic SARS-CoV-2 infection in a cohort of at-risk healthcare workers. Baseline and longitudinal assays will determine the frequency and magnitude of anti-spike glycoprotein antibodies to the seasonal HCoV-OC43, HCoV-HKU1, HCoV-229E, and HCoV-NL63, and may inform whether pre-existing antibodies to these human coronaviruses are associated with altered COVID-19 disease course. Finally, this study will evaluate whether pre-existing immune responses to seasonal HCoVs affect the magnitude and duration of antibody and T cell responses to SARS-CoV-2 vaccination, adjusting for demographic covariates.
SARS-CoV-2 是一种新近出现的大流行冠状病毒(CoV),能够引起严重的呼吸道疾病。然而,相当数量的感染者表现为无症状或症状轻微。在这项对高危医护人员(HCWs)的前瞻性评估中,我们旨在确定先前季节性人类冠状病毒(HCoV)感染的抗体或 T 细胞反应是否会影响对 SARS-CoV-2 感染或疫苗接种的免疫或临床反应。
一组 300 名医护人员在研究开始时被确认为 SARS-CoV-2 暴露阴性,将进行长达 1 年的随访,每月进行 SARS-CoV-2 刺突蛋白和针对四种主要季节性人类冠状病毒(HCoV-OC43、HCoV-HKU1、HCoV-229E 和 HCoV-NL63)的 IgM 和 IgG 抗体的血清学分析。参与者将每月完成问卷,询问有关 2019 年冠状病毒病(COVID-19)暴露风险的问题,并至少每两周两次和出现任何症状的任何一天完成标准化、经过验证的症状问卷(评分病毒性呼吸道疾病症状、强度和严重程度)。如果参与者出现符合 COVID-19 的症状,将随时进行 SARS-CoV-2 PCR 检测。对于那些血清学转换和/或 SARS-CoV-2 PCR 检测呈阳性的个体,或接种 SARS-CoV-2 疫苗的个体,将在参与者的冷冻保存外周血单核细胞(PBMC)上进一步研究针对 SARS-CoV-2 肽库的 T 细胞活化和细胞因子产生,并分析自然杀伤细胞数量和功能。在这项研究的第一年之后,我们将进一步分析那些 COVID-19 检测呈阳性的参与者,和/或已接种授权/许可的 SARS-CoV-2 疫苗的参与者,每季度(第 2 年)和每半年(第 3 年和第 4 年)进行分析,以调查免疫反应的持久性。
本研究将确定高危医护人员队列中无症状和症状轻微 SARS-CoV-2 感染的频率。基线和纵向检测将确定针对季节性 HCoV-OC43、HCoV-HKU1、HCoV-229E 和 HCoV-NL63 的抗刺突糖蛋白抗体的频率和幅度,并可能表明这些人类冠状病毒的预先存在抗体是否与改变的 COVID-19 病程有关。最后,本研究将评估针对季节性 HCoVs 的预先存在的免疫反应是否影响 SARS-CoV-2 疫苗接种的抗体和 T 细胞反应的幅度和持续时间,并调整人口统计学协变量。