Abstract P1063: Association of Demographic and Clinical Factors with SARS-CoV-2 Anti-Nucleocapsid Antibody Response Among Previously Infected US Adults: The C4R Study
Background: Despite the availability of effective vaccines and a recent decrease in annual deaths, coronavirus disease-2019 (COVID-19) remains a leading cause of death. Serological studies of anti-nucleocapsid (N) antibody response to infection provide insights into host immunobiology of adaptive immune response, which holds promise for identifying high-risk individuals for adverse acute and chronic COVID-19 outcomes. Hypothesis: Among participants previously infected with SARS-CoV-2, traditional vascular disease risk factors are associated with higher anti-N antibodies while vaccination is associated with lower anti-N antibodies. Methods: Among previously infected participants, anti-N antibodies were measured from dried blood spots collected between February 2021-February 2023 among 1,419 Collaborative Cohort of Cohorts for COVID-19 Research (C4R) participants with prior SARS-CoV-2 infection. We measured anti-N IgG antibodies reported as median fluorescence intensity (MFI) units; reactivity (i.e., seropositivity) was defined based on MFI above a validated threshold. Vascular disease risk factors were assessed via pre-pandemic in-person examination, questionnaires, and medical record review. Multivariable generalized linear models regressed anti-N reactivity (modified Poisson) or LN transformed MFI (linear). Results: Among 1,419 participants with prior infection, mean age (standard deviation) was 65.8(12.1) years, 61% were women, and 42.8% were self-reported from a race/ethnicity minority group. Participant reactivity to nucleocapsid peaked at 69% by 4 months post-infection and waned to only 44% ≥12 months after infection. After multivariable adjustment, higher anti-N antibody response was associated with older age, Hispanic (vs. White) or American Indian (vs. White) race/ethnicity, lower income and education, former smoking, and higher anti-spike antibody levels. Asian race (vs. White) and vaccination ( even after infection ) were associated with lower nucleocapsid reactivity; common cardiometabolic co-morbidities were not associated with anti-N reactivity or levels (Figures 1 and 2). Conclusions: Among participants previously infected with SARS-CoV-2, select sociodemographic and behavioral risk factors were associated with higher anti-N antibody levels while vaccination was associated with lower anti-N antibody levels. The observation that vaccination, even after infection, is related to lower anti-N antibody levels merits further investigation.
Authors
- Jean M. Rock
- John S. Kim (ORCID: https://orcid.org/0000-0002-8887-150X)
- Rachel Bievenue
- Rebekah Boyle
- Elizabeth A. Regan (ORCID: https://orcid.org/0000-0003-0624-9184)
- Ryan T. Demmer (ORCID: https://orcid.org/0000-0003-3429-0379)
- Sally E Morganroth
- Mitchell S.V. Elkind (ORCID: https://orcid.org/0000-0003-2562-1156)
- Mary Cushman (ORCID: https://orcid.org/0000-0002-7871-6143)
- Norrina B. Allen (ORCID: https://orcid.org/0000-0002-6993-4384)
- Carmen R. Isasi (ORCID: https://orcid.org/0000-0003-2700-9593)
- Alka M. Kanaya (ORCID: https://orcid.org/0000-0002-8903-1457)
- Joel Henderson (ORCID: https://orcid.org/0000-0002-9178-1708)
- Laura M. Raffield (ORCID: https://orcid.org/0000-0002-7892-193X)
- Victor E. Ortega (ORCID: https://orcid.org/0000-0002-3962-0528)
- Russell P. Tracy (ORCID: https://orcid.org/0000-0002-0080-2420)
- Margaret F. Doyle (ORCID: https://orcid.org/0000-0001-6769-5386)
- Barry J. Make (ORCID: https://orcid.org/0000-0003-4349-8745)
- Elizabeth C. Oelsner (ORCID: https://orcid.org/0000-0002-7481-9671)
- Christina Wu (ORCID: https://orcid.org/0000-0001-6369-6189)
- Vanessa Xanthakis (ORCID: https://orcid.org/0000-0002-7352-621X)
- Pallavi Balte (ORCID: https://orcid.org/0000-0001-5610-3744)
- Linda M. Styer
- Prescott G. Woodruff (ORCID: https://orcid.org/0000-0003-3176-0603)
- Taison D. Bell
- Amber Pirzada (ORCID: https://orcid.org/0000-0003-0526-3611)
- Russell Bowler
- Shelley A. Cole (ORCID: https://orcid.org/0000-0002-2651-0127)
- Namratha R. Kandula (ORCID: https://orcid.org/0000-0003-2570-3426)
- Pamela J. Schreiner (ORCID: https://orcid.org/0000-0002-9920-6257)
- Yifei Sun (ORCID: https://orcid.org/0000-0002-6961-5500)
- Michaela Restivo Anderson (ORCID: https://orcid.org/0000-0001-9274-7643)
- Virginia J. Howard (ORCID: https://orcid.org/0000-0003-4912-9975)
- Nicholas John Mantis (ORCID: https://orcid.org/0000-0002-5083-8640)
- David A. Schwartz (ORCID: https://orcid.org/0000-0001-6743-8443)
- Joyce Lee (ORCID: https://orcid.org/0000-0002-5758-8365)
- Joe Coresh
Institutions
- University of Vermont (US)
- Northwestern University (US)
- University of North Carolina at Chapel Hill (US)
- Texas Biomedical Research Institute (US)
- New York State Department of Health (US)
- Albert Einstein College of Medicine (US)
- Mayo Clinic (US)
- City College of San Francisco (US)
- University of Pittsburgh (US)
- University of California, San Francisco (US)
- University of Virginia Health System (US)
- University of Minnesota System (US)
- National Jewish Health (US)
- University of Illinois Chicago (US)
- Boston University Academy (US)
- Mayo Clinic Hospital (US)
- New York University Langone Orthopedic Hospital (US)
- University of Colorado Anschutz Medical Campus (US)
- Columbia University (US)
- University of Pennsylvania (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- Circulation
- Published
- 2025-03-11
- DOI
- https://doi.org/10.1161/cir.151.suppl_1.p1063
- Primary Topic
- SARS-CoV-2 and COVID-19 Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00