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Comparison of IgG and neutralizing antibody responses after one or two doses of COVID-19 mRNA vaccine in previously infected and uninfected individuals.
Demonbreun, Alexis R; Sancilio, Amelia; Velez, Matt P; Ryan, Daniel T; Saber, Rana; Vaught, Lauren A; Reiser, Nina L; Hsieh, Ryan R; D'Aquila, Richard T; Mustanski, Brian; McNally, Elizabeth M; McDade, Thomas W.
  • Demonbreun AR; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, USA.
  • Sancilio A; Department of Pharmacology, Northwestern University Feinberg School of Medicine, USA.
  • Velez MP; Department of Anthropology and Institute for Policy Research, Northwestern University, 1810 Hinman Avenue, Evanston, IL 60208 USA.
  • Ryan DT; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, USA.
  • Saber R; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, USA.
  • Vaught LA; Institute for Sexual and Gender Minority Health and Wellbeing and Department of Medical Social Sciences, Northwestern University, USA.
  • Reiser NL; Institute for Sexual and Gender Minority Health and Wellbeing and Department of Medical Social Sciences, Northwestern University, USA.
  • Hsieh RR; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, USA.
  • D'Aquila RT; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, USA.
  • Mustanski B; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, USA.
  • McNally EM; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, USA.
  • McDade TW; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, USA.
EClinicalMedicine ; 38: 101018, 2021 Aug.
Article in English | MEDLINE | ID: covidwho-1397304
ABSTRACT

BACKGROUND:

Recent reports have suggested that among individuals previously infected with SARS-CoV-2, a single mRNA vaccine dose is sufficient to elicit high levels of immunity.

METHODS:

We compared anti-SARS-CoV-2 spike receptor binding domain (RBD) IgG antibody concentrations and antibody-mediated neutralization of spike-angiotensin-converting enzyme (ACE2) receptor binding in vitro following vaccination of non-hospitalized participants by sero-status and acute virus diagnosis history. Participants were analysed before and after mRNA vaccination (BNT162b2/Pfizer or mRNA-1273/Moderna) in a community-based, home-collected, longitudinal serosurvey in the Chicago area (USA); none reported hospitalization for COVID-19. Samples were collected in January and February 2021. Before vaccination, some reported prior positive acute viral diagnostic testing and were seropositive (COVID-19+); the others who did not report acute viral diagnostic testing were categorized as seropositive or seronegative based on anti-spike RBD IgG test results.

FINDINGS:

Of 307 unique vaccine recipients, 46 reported a prior COVID-19 diagnosis and were seropositive (COVID-19 +). Of the 261 with no history of acute viral diagnostic testing, 117 were seropositive and 144 seronegative before vaccination. The median age was 38 years (range 21-83) with 67 female and 33% male; 40% were non-White. Responses were evaluated after one (n = 142) or two (n = 191) doses of BNT162b2 or mRNA-1273 vaccine. After one dose, median post-vaccine IgG concentration and percent surrogate neutralization were each significantly higher among the COVID-19+ (median 48·2 µg/ml, IgG; > 99.9% neutralization) compared to the seropositives (3·6 µg /ml IgG; 56.5% neutralization) and seronegatives (2·6 µg /ml IgG; 38·3% neutralization). The latter two groups reached > 95% neutralization after the second vaccine dose.

INTERPRETATION:

After one dose of mRNA vaccine, individuals previously diagnosed with COVID-19 responded with high levels of anti-RBD IgG and surrogate neutralization of spike-ACE2 interaction. One dose of mRNA vaccine was not sufficient to generate comparably high responses among most persons previously infected with SARS-CoV-2 without a clinical COVID-19 diagnosis, nor among seronegative persons.

FUNDING:

National Science Foundation 2035114, NIH 3UL1TR001422-06S4, and Northwestern University Office of Research.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal: EClinicalMedicine Year: 2021 Document Type: Article Affiliation country: J.eclinm.2021.101018

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Language: English Journal: EClinicalMedicine Year: 2021 Document Type: Article Affiliation country: J.eclinm.2021.101018