# Neutralizing antibody response to Omicron subvariants BA.1 and BA.5 in children and adolescents following the two-dose CoronaVac protocol (Immunita-002, Brazil): a 12-month longitudinal study

**Authors:** Camila Amormino Corsini, Guilherme Rodrigues Fernandes Campos, Priscila Fernanda da Silva Martins, Priscilla Soares Filgueiras, Ana Esther de Souza Lima, Sarah Vieira Contin Gomes, Caroline De Almeida Leitao Curimbaba, Daniela Aparecida Lorencini, Eolo Morandi Junior, Victor Mattos da Silva, Maria Célia Cervi, Marcos de Carvalho Borges, Poliana Remundini de Lima, João Paulo Resende do Nascimento, Paulo Roberto Lopes Correa, Leda dos Reis Castilho, Jaquelline Germano de Oliveira, Olindo Assis Martins Filho, Maurício Lacerda Nogueira, Rafaella Fortini Queiroz e Grenfell

PMC · DOI: 10.3389/fimmu.2025.1589733 · Frontiers in Immunology · 2025-07-15

## TL;DR

This study shows that the CoronaVac vaccine induces strong and lasting neutralizing antibodies in children and adolescents against Omicron subvariants BA.1 and BA.5 for up to one year.

## Contribution

The study provides new longitudinal data on the immune response to CoronaVac in younger populations against Omicron subvariants.

## Key findings

- Neutralizing antibody titers increased significantly in both seronegative and seropositive children and adolescents after two doses of CoronaVac.
- Seroconversion rates for BA.5 rose to over 90% in children and adolescents one month post-vaccination and remained high for 12 months.
- No significant difference in neutralization was observed between BA.1 and BA.5 post-vaccination, suggesting similar effectiveness against both subvariants.

## Abstract

The covid-19 pandemic prompted an unprecedented global effort to develop and deploy vaccines, including CoronaVac, an inactivated virus-based vaccine. While these vaccines effectively reduced severe cases and hospitalizations, limited data exists on their immunogenicity in younger populations, particularly children and adolescents. Understanding the immune response in these groups is essential to guide vaccination strategies and assess protection against emerging variants of concern, such as Omicron subvariants BA.1 and BA.5. This study evaluated the neutralizing antibody response in children and adolescents aged 3–17 years over 12 months following the two-dose CoronaVac protocol in Brazil.

A cohort of 108 children (3–11 years) and adolescents (12–17 years) from Serrana, Brazil, received two doses of CoronaVac. Peripheral blood samples were collected at baseline, and at 1, 3, 6, and 12 months after the second dose. Participants were stratified by serostatus prior to vaccination. Neutralizing antibodies against Omicron BA.1 and BA.5 were assessed using microneutralization assays.

Neutralizing antibody titers increased significantly after vaccination in both seronegative and seropositive individuals. For seronegative participants, seroconversion rates for BA.5 rose from 16.6% pre-vaccination to 93.3% one month after the second dose in children, and from 50% to 92% in adolescents, with sustained levels for 12 months. Seropositive participants also showed enhanced antibody titers, particularly against BA.5. No significant differences in neutralization between BA.1 and BA.5 were observed post-vaccination, contrary to prior literature, suggesting uniform effectiveness against these subvariants.

This study demonstrates that CoronaVac significantly enhances and sustains neutralizing antibody titers in children and adolescents for up to one year, including against immune-evading subvariants like BA.5. The robust response highlights the vaccine’s potential as a critical tool for reducing SARS-CoV-2 transmission and preventing severe disease, particularly in regions with limited access to updated vaccines. Further studies with larger cohorts are needed to validate these findings and inform vaccination strategies for immunoresistant variants.

## Linked entities

- **Diseases:** covid-19 (MONDO:0100096)

## Full-text entities

- **Genes:** S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, N (nucleocapsid phosphoprotein) [NCBI Gene 43740575]
- **Diseases:** deaths (MESH:D003643), COVID-19 (MESH:D000086382), infected (MESH:D007239)
- **Chemicals:** BA.1 (MESH:C006646), DMEM (-), CO2 (MESH:D002245)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]
- **Cell lines:** HEK293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), Vero — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0059)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12306644/full.md

## References

65 references — full list in the complete paper: https://tomesphere.com/paper/PMC12306644/full.md

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Source: https://tomesphere.com/paper/PMC12306644