Modeling and predicting individual variation in COVID-19 vaccine-elicited antibody response in the general population

Nakamura, Naotoshi and Kobashi, Yurie and Kim, Kwang Su and Park, Hyeongki and Tani, Yuta and Shimazu, Yuzo and Zhao, Tianchen and Nishikawa, Yoshitaka and Omata, Fumiya and Kawashima, Moe and Yoshida, Makoto and Abe, Toshiki and Saito, Yoshika and Senoo, Yuki and Nonaka, Saori and Takita, Morihito and Yamamoto, Chika and Kawamura, Takeshi and Sugiyama, Akira and Nakayama, Aya and Kaneko, Yudai and Jeong, Yong Dam and Tatematsu, Daiki and Akao, Marwa and Sato, Yoshitaka and Iwanami, Shoya and Fujita, Yasuhisa and Wakui, Masatoshi and Aihara, Kazuyuki and Kodama, Tatsuhiko and Shibuya, Kenji and Iwami, Shingo and Tsubokura, Masaharu and Yoon, Dukyong (2024) Modeling and predicting individual variation in COVID-19 vaccine-elicited antibody response in the general population. PLOS Digital Health, 3 (5). e0000497. ISSN 2767-3170

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Abstract

As we learned during the COVID-19 pandemic, vaccines are one of the most important tools in infectious disease control. To date, an unprecedentedly large volume of high-quality data on COVID-19 vaccinations have been accumulated. For preparedness in future pandemics beyond COVID-19, these valuable datasets should be analyzed to best shape an effective vaccination strategy. We are collecting longitudinal data from a community-based cohort in Fukushima, Japan, that consists of 2,407 individuals who underwent serum sampling two or three times after a two-dose vaccination with either BNT162b2 or mRNA-1273. Using the individually reconstructed time courses of the vaccine-elicited antibody response based on mathematical modeling, we first identified basic demographic and health information that contributed to the main features of the antibody dynamics, i.e., the peak, the duration, and the area under the curve. We showed that these three features of antibody dynamics were partially explained by underlying medical conditions, adverse reactions to vaccinations, and medications, consistent with the findings of previous studies. We then applied to these factors a recently proposed computational method to optimally fit an “antibody score”, which resulted in an integer-based score that can be used as a basis for identifying individuals with higher or lower antibody titers from basic demographic and health information. The score can be easily calculated by individuals themselves or by medical practitioners. Although the sensitivity of this score is currently not very high, in the future, as more data become available, it has the potential to identify vulnerable populations and encourage them to get booster vaccinations. Our mathematical model can be extended to any kind of vaccination and therefore can form a basis for policy decisions regarding the distribution of booster vaccines to strengthen immunity in future pandemics.

Item Type: Article
Subjects: Eprint Open STM Press > Multidisciplinary
Depositing User: Unnamed user with email admin@eprint.openstmpress.com
Date Deposited: 06 May 2024 09:45
Last Modified: 06 May 2024 09:45
URI: http://library.go4manusub.com/id/eprint/2165

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