Abstract
COVID-19 mRNA vaccines are highly effective at preventing COVID-19. Prior studies have found detectable SARS-CoV-2 IgG antibodies in oral mucosal specimens of participants with history of COVID-19. To assess the development of oral SARS-CoV-2 IgG antibodies among people who received either the Moderna or Pfizer/BioNTech COVID-19 vaccination series, we developed a novel SARS-CoV-2 IgG enzyme-linked immunosorbent assay (ELISA) to quantify the concentrations of oral and nasal mucosal SARS-CoV-2 IgG levels. We enrolled 52 participants who received the Moderna vaccine and 80 participants who received the Pfizer/BioNTech vaccine. Oral mucosal specimens were self-collected by participants prior to or on the day of vaccination, and on days 5, 10, 15, and 20 following each vaccination dose and 30, 60, and 90 days following the second vaccination dose. A subset of the cohort provided additional nasal mucosal specimens at every time point. All participants developed detectable oral mucosal SARS-CoV-2 IgG antibodies by 15 days after the first vaccination dose. There were no significant differences in oral mucosal antibody concentrations once participants were fully vaccinated in the Moderna and Pfizer/BioNTech vaccines. Oral or nasal mucosal antibody testing could be an inexpensive and less invasive alternative to serum antibody testing. Further research is needed to understand the duration of detectable oral or nasal mucosal antibodies and how antibody concentrations change with time.
Highlights
COVID-19 mRNA vaccines are highly effective at preventing COVID-19
Earlier work from our group demonstrated that an enzyme-linked immunosorbent assay (ELISA)-based qualitative assay can reliably detect the presence of SARS-CoV-2 IgG antibodies targeting spike proteins S1 and S2 from self-collected oral mucosal specimens among participants previously infected with SARS-CoV-25
We found that SARS-CoV-2 IgG antibodies can be detected and quantified in self-collected oral and nasal mucosal specimens following vaccination with a COVID-19 mRNA vaccine
Summary
Prior studies have found detectable SARS-CoV-2 IgG antibodies in oral mucosal specimens of participants with history of COVID-19. To assess the development of oral SARS-CoV-2 IgG antibodies among people who received either the Moderna or Pfizer/BioNTech COVID-19 vaccination series, we developed a novel SARSCoV-2 IgG enzyme-linked immunosorbent assay (ELISA) to quantify the concentrations of oral and nasal mucosal SARS-CoV-2 IgG levels. Earlier work from our group demonstrated that an ELISA-based qualitative assay can reliably detect the presence of SARS-CoV-2 IgG antibodies targeting spike proteins S1 and S2 from self-collected oral mucosal specimens among participants previously infected with SARS-CoV-25. We aimed to assess whether (1) SARS-CoV-2 IgG antibodies targeting the spike protein are detectable in self-collected oral and nasal mucosal specimens following COVID-19 mRNA vaccination; and (2) a quantitative assay could measure changes in SARS-CoV-2 IgG antibodies in oral and nasal mucosal fluid over time among vaccinated participants
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