Severe Acute Respiratory Syndrome Coronavirus 2 Infection History and Antibody Response to 3 Coronavirus Disease 2019 Messenger RNA Vaccine Doses

Author:

Herring Meghan K1,Romine James K2ORCID,Wesley Meredith G1,Ellingson Katherine D2,Yoon Sarang K3,Caban-Martinez Alberto J4,Meece Jennifer5,Gaglani Manjusha67ORCID,Grant Lauren8,Olsho Lauren E W1,Tyner Harmony L9,Naleway Allison L10,Khan Sana M2,Phillips Andrew L3,Solle Natasha Schaefer4,Rose Spencer6,Mak Josephine8,Fuller Sammantha B1,Hunt Angela9,Kuntz Jennifer L10,Beitel Shawn2,Yoo Young M8,Zheng Pearl Q1,Arani Gayatri2,Lamberte Julie Mayo8,Edwards Taylor11,Thompson Mark G8,Sprissler Ryan11,Thornburg Natalie J8,Lowe Ashley A2,Pilishvili Tamara8,Uhrlaub Jennifer L2,Lutrick Karen12,Burgess Jefferey L2,Fowlkes Ashley L8

Affiliation:

1. Abt Associates , Rockville, Maryland , USA

2. Mel and Enid Zuckerman College of Public Health, University of Arizona , Tucson, Arizona , USA

3. Rocky Mountain Center for Occupational and Environmental Health, University of Utah Health , Salt Lake City, Utah , USA

4. University of Miami, Miller School of Medicine , Miami, Florida , USA

5. Marshfield Clinic , Marshfield, Wisconsin , USA

6. Baylor Scott and White Health , Temple, Texas , USA

7. Texas A&M University College of Medicine , Temple, Texas , USA

8. COVID-19 Response Team, Centers for Disease Control and Prevention , Atlanta, Georgia , USA

9. St. Luke's Regional Health Care System , Duluth, Minnesota , USA

10. Kaiser Permanente Northwest Center for Health Research , Portland, Oregon , USA

11. University of Arizona Genetics Core, Office for Research, Innovation and Impact, University of Arizona , Tucson, Arizona , USA

12. College of Medicine–Tucson, University of Arizona , Tucson, Arizona , USA

Abstract

Abstract Background Data on antibody kinetics are limited among individuals previously infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). From a cohort of healthcare personnel and other frontline workers in 6 US states, we assessed antibody waning after messenger RNA (mRNA) dose 2 and response to dose 3 according to SARS-CoV-2 infection history. Methods Participants submitted sera every 3 months, after SARS-CoV-2 infection, and after each mRNA vaccine dose. Sera were tested for antibodies and reported as area under the serial dilution curve (AUC). Changes in AUC values over time were compared using a linear mixed model. Results Analysis included 388 participants who received dose 3 by November 2021. There were 3 comparison groups: vaccine only with no known prior SARS-CoV-2 infection (n = 224); infection prior to dose 1 (n = 123); and infection after dose 2 and before dose 3 (n = 41). The interval from dose 2 and dose 3 was approximately 8 months. After dose 3, antibody levels rose 2.5-fold (95% confidence interval [CI] = 2.2–3.0) in group 2 and 2.9-fold (95% CI = 2.6–3.3) in group 1. Those infected within 90 days before dose 3 (and median 233 days [interquartile range, 213–246] after dose 2) did not increase significantly after dose 3. Conclusions A third dose of mRNA vaccine typically elicited a robust humoral immune response among those with primary vaccination regardless of SARS-CoV-2 infection >3 months prior to boosting. Those with infection <3 months prior to boosting did not have a significant increase in antibody concentrations in response to a booster.

Funder

CDC

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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