Abstract
Two-dose messenger RNA vaccines against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are highly effective in preventing symptomatic COVID-19 infection. However, the durability of protection is not known, nor is the effectiveness against emerging viral variants. Additionally, vaccine responses may differ based on prior SARS-CoV-2 exposure history. To investigate protection against SARS-CoV-2 variants we measured binding and neutralizing antibody responses following both vaccine doses. We document significant declines in antibody levels three months post-vaccination, and reduced neutralization of emerging variants, highlighting the need to identify correlates of clinical protection to inform the timing of and indications for booster vaccination.
© 2021. The Author(s).
Publication types
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Comparative Study
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Adult
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Angiotensin-Converting Enzyme 2 / metabolism*
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Antibodies, Neutralizing / analysis*
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Antibodies, Neutralizing / metabolism
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Antibodies, Viral / analysis
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Antibodies, Viral / metabolism
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COVID-19 / immunology
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COVID-19 / metabolism
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COVID-19 / prevention & control*
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COVID-19 Nucleic Acid Testing
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COVID-19 Vaccines / administration & dosage
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COVID-19 Vaccines / immunology
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Female
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Humans
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Immunoglobulin G / analysis
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Immunoglobulin G / metabolism
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Male
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Middle Aged
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SARS-CoV-2 / immunology*
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Spike Glycoprotein, Coronavirus / metabolism
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Time Factors
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Vaccination
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Vaccines, Synthetic / administration & dosage*
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Vaccines, Synthetic / immunology
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Young Adult
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mRNA Vaccines
Substances
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Antibodies, Neutralizing
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Antibodies, Viral
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COVID-19 Vaccines
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Immunoglobulin G
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Spike Glycoprotein, Coronavirus
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Vaccines, Synthetic
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ACE2 protein, human
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Angiotensin-Converting Enzyme 2