# Variant-Specific Kinetics of SARS-CoV-2 Anti-Nucleocapsid Antibodies and Household Transmission in Families During Anchestral, Alpha, Delta and Omicron Periods

**Authors:** Filippos Filippatos, Elizabeth-Barbara Tatsi, Vassiliki Syriopoulou, Athanasios Michos

PMC · DOI: 10.3390/life16030470 · 2026-03-13

## TL;DR

This study shows how SARS-CoV-2 antibody levels change over time in children and adults and how different virus variants affect household transmission.

## Contribution

The study reveals variant-specific antibody kinetics and the role of pediatric cases in household transmission during different SARS-CoV-2 waves.

## Key findings

- Anti-nucleocapsid antibody levels peaked at three months and declined, with 89.2% remaining seropositive at 12 months.
- Children had higher antibody levels than adults during Delta and Omicron periods, and pediatric cases increased household transmission risk.
- Antibody waning was faster in secondary cases and during Omicron, but slower in those with higher initial antibody levels.

## Abstract

To investigate SARS-CoV-2 antibody kinetics and household transmission, infected children along with their families were tested for anti-nucleocapsid antibodies at 1, 3, 6, 9 and 12 months post-SARS-CoV-2 infection during the Ancestral, Alpha, Delta, and Omicron waves. We prospectively included SARS-CoV-2 acute infected children (n = 189). After household recruitment (n = 76 households), the total study population was 228 children and 105 adults. The median age (IQR) of children and adults was 96 (115) months and 504 (96) months, respectively. Anti-nucleocapsid (anti-N) COI (cut-off index) titers peaked at three months post-infection and declined thereafter (p-value < 0.001), and 89.2% remained seropositive at 12 months. Children displayed significantly higher anti-N COI titers than adults during the Delta (p-value: 0.018) and Omicron (p-value: 0.047) periods. Household contact anti-N positivity (evidence of infection) was associated with pediatric index cases (aOR: 1.61, 95% CI: 1.11–2.35; p-value: 0.013) and elevated early anti-N COI titers (aOR: 1.24 per log10 unit, 95% CI: 1.05–1.48; p-value: 0.011). Higher secondary attacks were detected in Delta (aOR: 2.12, 95% CI: 1.19–3.77; p-value: 0.011) and Omicron (aOR: 2.75, 95% CI: 1.44–5.25; p-value: 0.002) compared to Ancestral. Waning of SARS-CoV-2 anti-N titers was faster in secondary cases (aHR: 1.62, 95% CI: 1.01–2.59; p-value: 0.047, Cox model) and during Omicron infection (aHR: 1.74 vs. Ancestral, 95% CI: 1.08–2.79; p-value: 0.023). In contrast, waning was slower in SARS-CoV-2 cases with higher baseline anti-N COI titers (aHR: 0.77, 95% CI: 0.64–0.93; p-value: 0.011). These findings demonstrate variant-specific, age-dependent antibody kinetics, emphasizing that pediatric index cases were associated with higher odds of household infection.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** N (nucleocapsid phosphoprotein) [NCBI Gene 43740575]
- **Diseases:** SARS-CoV-2 (MESH:D000086382), infected (MESH:D007239)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027493/full.md

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Source: https://tomesphere.com/paper/PMC13027493