Multiparametric Prediction Models for Coronavirus Disease 2019 Vaccine Selection: Results of a Comparative Population-Based Cohort Study

Abstract Background An understanding vaccine-dependent effects on protective and sustained humoral immune response is crucial to planning future vaccination strategies against coronavirus disease 2019 (COVID-19). Methods In this multicenter, population-based, cohort study including 4601 individuals...

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Veröffentlicht in:Clinical infectious diseases 2023-03, Vol.76 (5), p.816-823
Hauptverfasser: Sieghart, Daniela, Hana, Claudia A, Haslacher, Helmuth, Perkmann, Thomas, Heinz, Leonhard X, Fedrizzi, Clemens, Anderle, Karolina, Wiedermann, Ursula, Condur, Irina, Drapalik, Susanne, Steinbrecher, Helmut, Mrak, Daniel, Mucher, Patrick, Hasenoehrl, Timothy, Zrdavkovic, Andrej, Wagner, Barbara, Palma, Stefano, Jordakieva, Galateja, Jorda, Anselm, Firbas, Christa, Wagner, Angelika, Haiden, Nadja, Bergmann, Felix, Crevenna, Richard, Zeitlinger, Markus, Bonelli, Michael, Aletaha, Daniel, Radner, Helga
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Sprache:eng
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Zusammenfassung:Abstract Background An understanding vaccine-dependent effects on protective and sustained humoral immune response is crucial to planning future vaccination strategies against coronavirus disease 2019 (COVID-19). Methods In this multicenter, population-based, cohort study including 4601 individuals after primary vaccination against COVID-19 ≥ 4 months earlier we compared factors associated with residual antibody levels against severe acute respiratory syndrome coronavirus-2 receptor-binding domain (RBD) across different vaccination strategies (BNT162b2, mRNA-1273, or ChAdOx1). Results Our main model including 3787 individuals (2 × BNT162b2, n = 2271; 2 × mRNA-1273, n = 251; 2 × ChAdOx1, n = 1265), predicted significantly lower levels of anti-RBD antibodies after 6 months in individuals vaccinated with ChAdOx1 (392.7 binding antibody units per milliliter [BAU/mL]) compared with those vaccinated with BNT162b2 (1179.5 BAU/mL) or mRNA-1273 (2098.2 BAU/mL). Vaccine-dependent association of antibody levels was found for age with a significant predicted difference in BAU/ml per year for BNT162b2 (−21.5; 95% confidence interval [CI], −24.7 to −18.3) and no significant association for mRNA-1273 (−4.0; 95% CI, −20.0 to 12.1) or ChAdOx1 (1.7; 95% CI, .2 to 3.1). The predicted decrease over time since full immunization was highest in mRNA-1273 (−23.4; 95% CI, −31.4 to −15.4) compared with BNT162b2 (−5.9; 95% CI, −7 to −4.8). Conclusions Our study revealed population-based evidence of vaccine-dependent effects of age and time since full immunization on humoral immune response. Findings underline the importance of individualized vaccine selection, especially in elderly individuals. In this comparative, population-based study of 4601 individuals, we found vaccine-dependent effects of age and time since full immunization on humoral immune response. Our data provide evidence-based guidance on selection of vaccination strategy based on age and a predictive estimate of the expected duration of vaccination protection.
ISSN:1058-4838
1537-6591
DOI:10.1093/cid/ciac840