抗体
医学
免疫系统
免疫学
临床终点
接种疫苗
疫苗试验
病毒学
代理终结点
危险系数
疫苗效力
临床试验
内科学
置信区间
作者
Chong Ma,Jiejun Du,Lan Lan,Archana Kapoor,Gonzalo Pérez Marc,Gilberto Jimenez,C.J. Duncan,Nancy Le Cam,Nina Lin,Frances Priddy,Sanjay Garg,Sonia Stoszek,Christine A. Shaw,Jaya Goswami,Eleanor Wilson,Rituparna Das,Honghong Zhou,Lingyi Zheng
标识
DOI:10.1038/s41467-025-61153-x
摘要
Identifying an immunologic marker as a correlate of protection (CoP) for RSV vaccination is important. In the pivotal phase 3 trial, the mRNA-1345 vaccine demonstrated efficacy against RSV in older adults (NCT05127434). Here, we evaluate neutralizing antibodies (nAb) against RSV-A and -B, and IgG binding antibodies (bAb) to RSV fusion antigens as correlates of risk (CoR) and CoP against the pivotal trial's efficacy endpoints of RSV lower respiratory tract disease with ≥2 or ≥3 signs/symptoms (RSV-LRTD-2+ and -3 + ) and acute respiratory disease (RSV-ARD). Day 29 RSV nAb and prefusion (preF) IgG demonstrate consistent inverse correlates with RSV endpoint occurrence. Day 29 point estimates (95% CIs) of the hazard ratio of each endpoint (RSV-LRTD-2 + , RSV-LRTD-3 + , RSV-ARD) per 10-fold increase in RSV-A nAb are 0.44 (0.30-0.65), 0.41 (0.20-0.84), and 0.45 (0.28-0.71), respectively, similar to RSV-B nAb and preF IgG. These results demonstrate Day 29 RSV nAb and preF IgG are CoRs and support their role as CoPs against RSV endpoints.
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