Department of Epidemiology and Prevention, Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo, Japan.
AIDS Clinical Center, National Center for Global Health and Medicine, Tokyo, Japan.
J Infect Dis. 2023 Dec 20;228(12):1652-1661. doi: 10.1093/infdis/jiad317.
Data are limited on the role of preinfection humoral immunity protection against Omicron BA.5 infection and long coronavirus disease (COVID) development.
We conducted nested case-control analysis among tertiary hospital staff in Tokyo who donated blood samples in June 2022 (1 month before Omicron BA.5 wave), approximately 6 months after receiving a third dose of COVID-19 mRNA vaccine. We measured live virus-neutralizing antibody titers against wild type and Omicron BA.5, and anti-receptor-binding domain (RBD) antibody titers at preinfection, and compared them between cases and propensity-matched controls. Among the breakthrough cases, we examined association between preinfection antibody titers and incidence of long COVID.
Preinfection anti-RBD and neutralizing antibody titers were lower in cases than controls. Neutralizing titers against wild type and Omicron BA.5 were 64% (95% confidence interval [CI], 42%-77%) and 72% (95% CI, 53%-83%) lower, respectively, in cases than controls. Individuals with previous Omicron BA.1/BA.2 infections were more frequent among controls than cases (10.3% vs 0.8%), and their Omicron BA.5 neutralizing titers were 12.8-fold higher than infection-naive individuals. Among cases, preinfection antibody titers were not associated with incidence of long COVID.
Preinfection immunogenicity against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may play a role in protecting against the Omicron BA.5 infection but not preventing long COVID.
关于奥密克戎 BA.5 感染前的体液免疫保护作用以及长新冠发病的相关数据有限。
我们在东京的一家三级医院的工作人员中进行了嵌套病例对照分析,这些工作人员在 2022 年 6 月(奥密克戎 BA.5 浪潮前 1 个月)献血,大约在第三次接种 COVID-19 mRNA 疫苗后 6 个月。我们在感染前测量了针对野生型和奥密克戎 BA.5 的活病毒中和抗体滴度和抗受体结合域(RBD)抗体滴度,并将其与病例和倾向匹配的对照进行了比较。在突破性病例中,我们检查了感染前抗体滴度与长新冠发病之间的关联。
与对照组相比,病例组的感染前抗 RBD 和中和抗体滴度较低。与对照组相比,野生型和奥密克戎 BA.5 的中和滴度分别低 64%(95%置信区间,42%-77%)和 72%(95%置信区间,53%-83%)。对照组中既往有奥密克戎 BA.1/BA.2 感染的个体比病例组更为常见(10.3% vs. 0.8%),其奥密克戎 BA.5 中和滴度比无感染史的个体高 12.8 倍。在病例组中,感染前抗体滴度与长新冠发病无关。
针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的感染前免疫原性可能在预防奥密克戎 BA.5 感染方面发挥作用,但不能预防长新冠。