Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Science. 2022 Jan 7;375(6576):43-50. doi: 10.1126/science.abm3425. Epub 2021 Nov 23.
In the coronavirus efficacy (COVE) phase 3 clinical trial, vaccine recipients were assessed for neutralizing and binding antibodies as correlates of risk for COVID-19 disease and as correlates of protection. These immune markers were measured at the time of second vaccination and 4 weeks later, with values reported in standardized World Health Organization international units. All markers were inversely associated with COVID-19 risk and directly associated with vaccine efficacy. Vaccine recipients with postvaccination 50% neutralization titers 10, 100, and 1000 had estimated vaccine efficacies of 78% (95% confidence interval, 54 to 89%), 91% (87 to 94%), and 96% (94 to 98%), respectively. These results help define immune marker correlates of protection and may guide approval decisions for messenger RNA (mRNA) COVID-19 vaccines and other COVID-19 vaccines.
在冠状病毒功效(COVE)3 期临床试验中,疫苗接种者的中和抗体和结合抗体被评估为 COVID-19 疾病风险的相关因素,以及保护作用的相关因素。这些免疫标志物在第二次接种时和 4 周后进行测量,以标准化的世界卫生组织国际单位报告数值。所有标志物均与 COVID-19 风险呈负相关,与疫苗功效呈正相关。疫苗接种者的 50%中和滴度分别为 10、100 和 1000,其疫苗估计功效分别为 78%(95%置信区间,54 至 89%)、91%(87 至 94%)和 96%(94 至 98%)。这些结果有助于确定保护作用的免疫标志物相关性,并可能为信使 RNA(mRNA)COVID-19 疫苗和其他 COVID-19 疫苗的批准决策提供指导。