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Mrna 1273 spikevax

Manufactured by Moderna

MRNA-1273/Spikevax is a vaccine product developed by Moderna. It is a messenger RNA (mRNA) vaccine that provides instructions for human cells to produce a harmless piece of the SARS-CoV-2 spike protein, which then triggers an immune response. The core function of this product is to generate an immune response against the SARS-CoV-2 virus.

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2 protocols using mrna 1273 spikevax

1

Longitudinal SARS-CoV-2 Antibody Dynamics in Milk

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This prospective longitudinal cohort study is a follow-up study of the COVID MILK – POWER MILK study.34 (link) All samples were subjected to longitudinal analysis of specific antibodies against SARS-CoV-2 in human milk and serum after vaccination against COVID-19 with either BNT162b2/Comirnaty developed by Pfizer-BioNTech, mRNA-1273/Spikevax developed by Moderna, AZD1222/Vaxzevria developed by Oxford/AstraZeneca and Ad26.COV2.S developed by J&J/Janssen. Ethical approval was acquired from the Independent Ethics Committee of the Vrije Universiteit Medical Center (2020.425/NL74752.029.20). The study was conducted in accordance with the principles of the declaration of Helsinki and the ICH GCP Guidelines, and the Regulation on Medical Research involving Human subjects and reported in adherence to the CONSORT reporting guidelines.
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2

COVID-19 Vaccination Antibody Response in Breast Milk

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In this observational longitudinal case series we used samples from an existing prospective longitudinal study COVID MILK – POWER MILK (28 (link)). All participants were subjected to longitudinal analysis of specific antibodies against the SARS-CoV-2 spike-protein by ELISA and general SIgA1 Fab clonal profiling in human milk after vaccination against COVID-19 with BNT162b2/Comirnaty developed by Pfizer-BioNTech, mRNA-1273/Spikevax developed by Moderna or AZD1222/Vaxzevria developed by Oxford/AstraZeneca. Ethical approval was acquired from an Independent Ethics Committee (2020.425/NL74752.029.20). The study was conducted in accordance with the principles of the declaration of Helsinki and the ICH GCP Guidelines, and the Regulation on Medical Research involving Human subjects.
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