# Cellular Immunological Memory T Cells and IL15RA Gene Polymorphism in COVID-19 Vaccinated Individuals from Southern Brazil

**Authors:** Grazielle Motta Rodrigues, Pâmela Portela da Silva, Maria Clara de Freitas Pinho, Taís da Silveira Fischer, Fernanda de Paris, Fabrício Souza Campos, Arthur Bandeira de Mello Garcia, Lucas Fernandes Jataí, Patricia Ashton-Prolla, Fernanda Sales Luiz Vianna, Clévia Rosset

PMC · DOI: 10.3390/diagnostics16010089 · Diagnostics · 2025-12-26

## TL;DR

This study examines memory T cells and a genetic variant in vaccinated individuals from southern Brazil to understand immune responses and vaccine effectiveness.

## Contribution

The study explores the impact of IL15RA gene polymorphism on T cell memory in vaccinated individuals, revealing genotype-specific immune responses.

## Key findings

- A decrease in memory T cell subsets was observed in response to SARS-CoV-2 stimuli.
- Participants with the TT genotype showed increased CD8+ and CD4+ T cell subsets after specific vaccination regimens.
- Booster doses are suggested to maintain cellular immune protection against emerging variants.

## Abstract

Background: The development of safe and effective vaccines against SARS-CoV-2 was crucial for controlling COVID-19 and establishing long-lasting immune memory in the population. Methods: This study evaluated cellular immune memory in individuals vaccinated with different regimens in Rio Grande do Sul using flow cytometry. Additionally, the rs2228059 polymorphism in the IL15RA gene was genotyped. A total of 62 participants were randomly recruited. Results: A decrease in memory T cell subsets in response to SARS-CoV-2 stimuli was observed in total CD3+, CD4+, and CD8+ T cells. Regarding the timing of the last vaccine dose, 94.4% of participants had received their final COVID-19 vaccination at least two years prior to recruitment. The rs2228059 polymorphism was genotyped in 443 individuals from the Rio Grande do Sul population. Among participants who received the ChAdOx1/ChAdOx1/BNT162b2 vaccination regimen and carried the TT genotype, an increase in CD8+ naive, CD8+ effector and CD4+ naive subsets was observed in stimulated cells. Although preliminary, the results suggest no major differences between vaccination regimens. Conclusions: The progressive reduction in memory T cell counts supports the need for booster doses, which is essential not only in the context of new emerging variants but also especially to maintain adequate cellular immune protection.

## Linked entities

- **Genes:** IL15RA (interleukin 15 receptor subunit alpha) [NCBI Gene 3601]
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, IL15RA (interleukin 15 receptor subunit alpha) [NCBI Gene 3601] {aka CD215}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** COVID-19 (MESH:D000086382)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]
- **Mutations:** rs2228059

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12785960/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12785960/full.md

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Source: https://tomesphere.com/paper/PMC12785960