Surie Diya, Self Wesley H, Yuengling Katharine A, Lauring Adam S, Zhu Yuwei, Safdar Basmah, Ginde Adit A, Simon Samantha J, Peltan Ithan D, Brown Samuel M, Gaglani Manjusha, Ghamande Shekhar, Columbus Cristie, Mohr Nicholas M, Gibbs Kevin W, Hager David N, Prekker Matthew, Gong Michelle N, Mohamed Amira, Johnson Nicholas J, Steingrub Jay S, Khan Akram, Duggal Abhijit, Gordon Alexandra J, Qadir Nida, Chang Steven Y, Mallow Christopher, Felzer Jamie R, Kwon Jennie H, Exline Matthew C, Vaughn Ivana A, Ramesh Mayur, Papalambros Leigh, Mosier Jarrod M, Harris Estelle S, Baughman Adrienne, Cornelison Sydney A, Blair Paul W, Johnson Cassandra A, Lewis Nathaniel M, Ellington Sascha, Grijalva Carlos G, Talbot H Keipp, Casey Jonathan D, Halasa Natasha, Chappell James D, Rutkowski Rachel E, Ma Kevin C, Dawood Fatimah S
Coronavirus and Other Respiratory Viruses Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia.
Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
JAMA. 2025 Aug 30. doi: 10.1001/jama.2025.15896.
Respiratory syncytial virus (RSV) vaccines for adults aged 60 years or older became available in 2023. One dose is recommended for all adults aged 75 years or older and those aged 60 to 74 years at increased risk of severe RSV; however, duration of protection is unknown.
To evaluate RSV vaccine effectiveness against RSV-associated hospitalization among adults aged 60 years or older during 2 RSV seasons.
DESIGN, SETTING, AND PARTICIPANTS: A total of 6958 adults aged 60 years or older were included in this test-negative, case-control study if they were hospitalized with acute respiratory illness at any of 26 hospitals in 20 US states during the October 1, 2023, to March 31, 2024, or October 1, 2024, to April 30, 2025, RSV seasons and had respiratory virus testing within 10 days of illness onset. Case patients tested positive for RSV only; control patients tested negative for RSV, SARS-CoV-2, and influenza. Demographic and clinical data were obtained through patient interview and electronic health records.
Receipt of 1 RSV vaccine dose at least 14 days before illness onset.
Multivariable logistic regression was used to compare the odds of RSV vaccination among hospitalized cases and controls. Models were adjusted for age, sex, race and ethnicity, geographic region, and calendar month and year. Vaccine effectiveness was estimated as (1 - adjusted odds ratio) × 100%. Analyses were stratified by timing of RSV vaccine receipt (same vs prior season) relative to illness onset.
Of 6958 adults aged 60 years or older, 821 (11.8%) were RSV cases and 6137 (88.2%) were controls. A total of 1438 patients were Black (20.1%) and 4314 were White (62.0%); 3534 were female (50.8%). Median age was 72 years (IQR, 66-80 years) and 1829 adults (26.3%) were immunocompromised. A total of 63 cases (7.7%) and 966 controls (15.7%) were vaccinated. Estimated vaccine effectiveness against RSV-associated hospitalization was 58% (95% CI, 45%-68%) during 2 seasons and 69% (95% CI, 52%-81%) for same-season vaccination vs 48% (95% CI, 27%-63%; P = .06) for prior-season vaccination. Estimated vaccine effectiveness during 2 seasons was significantly lower among immunocompromised adults (30%; 95% CI, -9% to 55%) than immunocompetent adults (67%; 95% CI, 53%-77%; P = .02) and among those with cardiovascular disease (56%; 95% CI, 32%-72%) vs without (80%; 95% CI, 62%-90%; P = .03).
Respiratory syncytial virus vaccines prevented RSV-associated hospitalization during 2 seasons, although effectiveness was lower in patients with immunocompromise and cardiovascular disease than in those without these conditions. Ongoing monitoring is needed to determine the optimal RSV revaccination interval.
2023年有了针对60岁及以上成年人的呼吸道合胞病毒(RSV)疫苗。建议所有75岁及以上成年人以及60至74岁有严重RSV感染高风险的成年人接种一剂;然而,保护期尚不清楚。
评估RSV疫苗在两个RSV流行季节对60岁及以上成年人RSV相关住院治疗的有效性。
设计、地点和参与者:如果6958名60岁及以上成年人在2023年10月1日至2024年3月31日或2024年10月1日至2025年4月30日的RSV流行季节期间,在美国20个州的26家医院中的任何一家因急性呼吸道疾病住院,并且在发病后10天内进行了呼吸道病毒检测,则纳入这项检测阴性的病例对照研究。病例患者仅RSV检测呈阳性;对照患者RSV、SARS-CoV-2和流感检测均为阴性。通过患者访谈和电子健康记录获取人口统计学和临床数据。
在发病前至少14天接种一剂RSV疫苗。
采用多变量逻辑回归比较住院病例和对照中接种RSV疫苗的几率。模型根据年龄、性别、种族和民族、地理区域以及日历月和年份进行了调整。疫苗有效性估计为(1 - 调整后的比值比)×100%。分析按RSV疫苗接种时间(同季与上一季)相对于发病时间进行分层。
在69,58名60岁及以上成年人中,821人(11.8%)为RSV病例,6137人(88.2%)为对照。共有1438名患者为黑人(20.1%),4314名患者为白人(62.0%);3534名患者为女性(50.8%)。中位年龄为72岁(四分位间距,66 - 80岁),1829名成年人(26.3%)免疫功能低下。共有63例病例(7.7%)和966名对照(15.7%)接种了疫苗。在两个流行季节期间,估计RSV疫苗对相关住院治疗的有效性为58%(95%置信区间,45% - 68%),同季接种为69%(95%置信区间,52% - 81%),而上一季接种为48%(95%置信区间,27% - 63%;P = 0.06)。在免疫功能低下的成年人中,两个流行季节期间估计的疫苗有效性(30%;95%置信区间, - 9%至55%)显著低于免疫功能正常的成年人(67%;95%置信区间:53% - 77%;P = 0.02),在有心血管疾病的成年人中(56%;95%置信区间,32% - 72%)低于无心血管疾病的成年人(80%;95%置信区间,62% - 90%;P = 0.03)。
呼吸道合胞病毒疫苗在两个流行季节预防了RSV相关住院治疗,尽管免疫功能低下和有心血管疾病的患者的有效性低于无这些情况的患者。需要持续监测以确定最佳的RSV再次接种间隔。