A Longitudinal Seroconversion Panel Shows Anti-SARS-CoV-2 Antibody Levels up to 6.5 Months After Vaccination with mRNA-1273 (Moderna)

Author:

Belda Francisco1,Mora Oscar1ORCID,Christie Rebecca2,Crowley Michael2

Affiliation:

1. Research and Development, Bio Supplies Division, Grifols, Sant Cugat del Vallès (Barcelona), Spain

2. Access Biologicals, Vista, CA, USA

Abstract

BACKGROUND Vaccines have emerged as a crucial tool in combatting the COVID-19 pandemic particularly those based on SARS-CoV-2 S-protein mRNA. A crucial aspect of vaccine efficacy is the duration of antibody responses. In this study, a seroconversion panel was created to assess antibody responses to the mRNA-1273 vaccine over time (6.5 months). METHODS Blood samples collected from 15 healthy adult participants prior to and up to 6.5 months after vaccination with the mRNA-1273 vaccine (Moderna). Serum from these blood samples were analyzed for anti-SARS-CoV-2 antibody activity by chemiluminescent immunoassay. RESULTS The immunoassay results showed that one participant was positive for anti-SARS-CoV-2 antibodies prior to vaccination indicating a prior infection. All participants showed a positive antibody response after the first vaccination. Highest antibody responses were seen after the second dose (41-45 days from the first dose). Subsequent samples collected at 69-75 days, 130-135 days, and 221-229 days after the first vaccination showed positive responses but a biphasic decline in the levels of anti-SARS-CoV-2 antibodies. CONCLUSIONS Declining antibody levels in these participants support the use of booster vaccination to increase antibody levels 4-6 months after the initial vaccine series and continued monitoring to assess the durability of COVID-19 vaccine responses. These results are in agreement with other studies showing antibody persistence but declining the antibody levels in the months after immunization with mRNA-based vaccines. The seroconversion panels described here could be useful in the development of antibody assays and in the assessment of the duration of antibody responses to vaccine boosters compared to the initial vaccine series. This panel could also be used to assess antibody activity against emerging viral variants (eg B.1.1.529 [Omicron] and its subvariants) compared to earlier variants.

Funder

Access Biologicals

Grifols

Publisher

SAGE Publications

Subject

Hematology

Reference17 articles.

1. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China

2. Moderna COVID-19 Vaccine. 2021 13 December 2021 16 December 2021]; Available from: https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/moderna-covid-19-vaccine.

3. Emergency use authorization (EUA) for an unapproved produce: Review memorandum - Moderna COVID-19 vaccine/mRNA-1273; 18 December 2020. Accessed 30 August 2022; Available from: https://www.fda.gov/media/144673/download.

4. Coronavirus (COVID-19) update: FDA takes additional actions on the use of a booster dose for COVID-19 vaccines; 2021. Updated 20 October 2021. Accessed 30 August 2022; Available from: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-takes-additional-actions-use-booster-dose-covid-19-vaccines.

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