Time since SARS-CoV-2 infection and humoral immune response following BNT162b2 mRNA vaccination
Autor: | Brent Appelman, Karlijn van der Straten, A.H. Ayesha Lavell, Michiel Schinkel, Marleen A. Slim, Meliawati Poniman, Judith A. Burger, Melissa Oomen, Khadija Tejjani, Alexander P.J. Vlaar, W. Joost Wiersinga, Yvo M. Smulders, Lonneke A. van Vught, Rogier W. Sanders, Marit J. van Gils, Marije K. Bomers, Jonne J. Sikkens, Diederik van de Beek, Marije K Bomers, Justin de Brabander, Matthijs C Brouwer, David TP Buis, Nora Chekrouni, Marit J van Gils, Menno D de Jong, AH Ayesha Lavell, Niels van Mourik, Sabine E Olie, Edgar JG Peters, Tom DY Reijnders, Alex R Schuurman, Jonne J Sikkens, Marleen A Slim, Yvo M Smulders, Alexander PJ Vlaar, Lonneke A van Vught, W Joost Wiersinga |
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Přispěvatelé: | Internal medicine, AII - Infectious diseases, ACS - Diabetes & metabolism, ACS - Atherosclerosis & ischemic syndromes, Center of Experimental and Molecular Medicine, Graduate School, Medical Microbiology and Infection Prevention, Intensive Care Medicine, ACS - Microcirculation, Infectious diseases, APH - Personalized Medicine, APH - Health Behaviors & Chronic Diseases, ACS - Pulmonary hypertension & thrombosis |
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Adult
Male Medicine (General) COVID-19 Vaccines Time Factors Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Health Personnel Antibodies Viral General Biochemistry Genetics and Molecular Biology Neutralization Neutralisation Immune system R5-920 Medicine Humans Prospective Studies Humoral immune response BNT162 Vaccine Netherlands Messenger RNA business.industry SARS-CoV-2 Confounding Spike Protein COVID-19 General Medicine Middle Aged Antigen binding Immunity Humoral Vaccination Treatment Outcome Immunoglobulin G Immunology Antibody Formation Female BNT162b2 business Vaccine |
Zdroj: | EBioMedicine, 72:103589. Elsevier BV EBioMedicine, Vol 72, Iss, Pp 103589-(2021) Amsterdam UMC COVID-19 S3/HCW study group 2021, ' Time since SARS-CoV-2 infection and humoral immune response following BNT162b2 mRNA vaccination ', EBioMedicine, vol. 72, 103589 . https://doi.org/10.1016/j.ebiom.2021.103589 |
ISSN: | 2352-3964 |
DOI: | 10.1016/j.ebiom.2021.103589 |
Popis: | Background: To optimise the use of available SARS-CoV-2 vaccines, some advocate delaying second vaccination for individuals infected within six months. We studied whether post-vaccination immune response is equally potent in individuals infected over six months prior to vaccination. Methods: We tested serum IgG binding to SARS-CoV-2 spike protein and neutralising capacity in 110 healthcare workers, before and after both BNT162b2 messenger RNA (mRNA) vaccinations. We compared outcomes between participants with more recent infection (n = 18, median two months, IQR 2-3), with infection-vaccination interval over six months (n = 19, median nine months, IQR 9-10), and to those not previously infected (n = 73). Findings: Both recently and earlier infected participants showed comparable humoral immune responses after a single mRNA vaccination, while exceeding those of previously uninfected persons after two vaccinations with 2.5 fold (p = 0.003) and 3.4 fold (p < 0.001) for binding antibody levels, and 6.4 and 7.2 fold for neutralisation titres, respectively (both p < 0.001). The second vaccine dose yielded no further substantial improvement of the humoral response in the previously infected participants (0.97 fold, p = 0.92), while it was associated with a 4 fold increase in antibody binding levels and 18 fold increase in neutralisation titres in previously uninfected participants (both p < 0.001). Adjustment for potential confounding of sex and age did not affect these findings. Interpretation: Delaying the second vaccination in individuals infected up to ten months prior may constitute a more efficient use of limited vaccine supplies. Funding: Netherlands Organization for Health Research and Development ZonMw; Corona Research Fund Amsterdam UMC; Bill & Melinda Gates Foundation. |
Databáze: | OpenAIRE |
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