Longitudinal analysis of antibody titers after primary and booster mRNA COVID-19 vaccination can identify individuals at risk for breakthrough infection
Hyeongki ParkiD, Naotoshi NakamuraiD, Shô MiyamotoiD, Yoshitaka SatoiD, Kwang Su KimiD, Kosaku KitagawaiD, Yurie KobashiiD, Yuta TaniiD, Yuzo ShimazuiD, Tianchen ZhaoiD, Yoshitaka NishikawaiD, Fumiya OmataiD, Moe KawashimaiD, Toshiki AbeiD, Yoshika SaitoiD, Saori NonakaiD, Morihito TakitaiD, Chika YamamotoiD, Hiroshi MoriokaiD, Katsuhiro KatoiD, Ken SagouiD, Tetsuya Yagi, Takeshi KawamuraiD, Akira SugiyamaiD, Aya NakayamaiD, , Masaharu TsubokuraiD
Abstract
A key issue in the post-COVID-19 era is the ongoing administration of COVID-19 vaccines. Repeated vaccination is essential for preparing against currently circulating and newly emerging SARS-CoV-2 variants while enabling people to continue with daily life. Optimizing vaccination strategies is crucial to efficiently manage medical resources and establish an effective vaccination framework. Therefore, it is important to quantitatively understand vaccine-induced immunity dynamics and to be able to identify poor responders with lower sustained antibody titers as potential priorities for revaccination. We investigated longitudinal antibody titer data in a cohort of 2,526 people in Fukushima, Japan, from April 2021 to November 2022 for whom basic demographic and health information was available. Using mathematical modeling and machine learning, we stratified the time-course patterns of antibody titers after 2 primary doses and 1 booster dose of mRNA COVID-19 vaccines. We identified 3 notable populations, which we refer to as the durable, the vulnerable, and the rapid-decliner populations, approximately half of which remained in the same population after the booster dose. Notably, the rapid-decliner population experienced earlier infections than the others. Furthermore, when comparing IgG(S) titers, IgA(S) titers, and T-spot counts between participants who experienced breakthrough infections after booster vaccination and those who did not, we found that IgA(S) titers were significantly lower in breakthrough infected participants during the early stage after booster vaccination. Our computational approach is adaptable to various types of vaccinations. This flexibility can inform policy decisions on vaccine distribution to enhance immunity both in future pandemics and in the post-COVID-19 era.
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