Boehme Amelia, Harvey Raymond A, Madsen Ann, Rubens Lexie, Toyip Astra, Batech Michael, Ricci Deborah, Nyaku Mawuli
Aetion Inc., New York, NY, United States.
Johnson & Johnson Innovative Medicine, Spring House, PA, United States.
Front Public Health. 2024 Dec 4;12:1501919. doi: 10.3389/fpubh.2024.1501919. eCollection 2024.
The goal of this FDA-committed, post authorization study was to assess the real-world effectiveness of Ad26.COV2.S in preventing observed COVID-19 disease in individuals in the United States interacting with the healthcare system who were vaccinated according to the national immunization recommendations.
The study cohort consisted of individuals ≥18 years in the U.S. between March 1, 2021 and July 31, 2022. Two exposure groups were considered: those who received a single dose of COVID-19 Ad26.COV2.S vaccine and individuals who were unvaccinated. Individuals eligible for the referent group, defined as those who were unvaccinated, were identified through exact matching on age, sex, location, and Gagne comorbidity score. Propensity-score (PS) matched Cox proportional hazards models were used to evaluate COVID-19 related outcomes.
A total of 478,162 vaccinated, and 1,897,759 risk set sampled (RSS) and PS-matched unvaccinated referent individuals were included. The vaccine effectiveness (VE) against any observed COVID-19 disease was 20% (95% CI, 19 to 21%). VE increased as the outcome severity increased. The VE against COVID-19 related hospitalizations was 43% (95% CI, 40 to 45%). VE was highest, 53% (95% CI, 42 to 61%), against all-cause mortality temporally associated with COVID-19. The results of subgroup analyses generally showed a similar pattern as the main analyses with VE increasing in parallel with seriousness of outcomes, albeit with lower VE in groups thought to be at higher risk of COVID-19.
This population-representative cohort study in U.S. clinical practice showed that a single dose of Ad26.COV2.S is effective for at least 12 months against several COVID-19 related outcomes. Individuals who were vaccinated with a single dose of Ad26.COV2.S were at lower risk for developing COVID-19, for being hospitalized for COVID-19, and for all-cause mortality temporally associated with COVID-19 compared to unvaccinated individuals in the U.S. during Alpha, Delta, and Omicron BA.1, BA.2, BA.212.1, and BA.5 variants circulation.
这项由美国食品药品监督管理局(FDA)委托开展的上市后授权研究的目的是评估Ad26.COV2.S疫苗在美国按照国家免疫建议接种疫苗、与医疗系统有接触的个体中预防观察到的新冠病毒病的实际效果。
研究队列包括2021年3月1日至2022年7月31日期间美国年龄≥18岁的个体。考虑了两个暴露组:接受单剂新冠病毒Ad26.COV2.S疫苗的个体和未接种疫苗的个体。通过年龄、性别、地点和加涅合并症评分的精确匹配确定符合作为参照组(定义为未接种疫苗的个体)条件的个体。采用倾向得分(PS)匹配的Cox比例风险模型评估与新冠病毒病相关的结局。
共纳入478,162名接种疫苗者,以及1,897,759名风险集抽样(RSS)且经PS匹配的未接种疫苗的参照个体。针对任何观察到的新冠病毒病的疫苗效力(VE)为20%(95%置信区间,19%至21%)。随着结局严重程度的增加,VE升高。针对与新冠病毒病相关住院治疗的VE为43%(95%置信区间,40%至45%)。针对与新冠病毒病在时间上相关的全因死亡率,VE最高,为53%(95%置信区间,42%至61%)。亚组分析结果总体上显示出与主要分析相似的模式,即VE随着结局严重程度的增加而平行升高,尽管在被认为感染新冠病毒病风险较高的组中VE较低。
这项在美国临床实践中具有人群代表性的队列研究表明,单剂Ad26.COV2.S疫苗对多种与新冠病毒病相关的结局至少12个月有效。与在美国阿尔法、德尔塔和奥密克戎BA.1、BA.2、BA.212.1和BA.5变异株流行期间未接种疫苗的个体相比,接种单剂Ad26.COV2.S疫苗的个体感染新冠病毒病、因新冠病毒病住院以及出现与新冠病毒病在时间上相关的全因死亡的风险较低。