# Influenza Vaccine Immunogenicity in Hemodialysis Patients

**Authors:** Anna-Polina Shurygina, Ekaterina Romanovskaya-Romanko, Vera Krivitskaya, Mariia Sergeeva, Janna Buzitskaya, Kirill Vasilyev, Marina Shuklina, Konstantin Vishnevskii, Dmitry Smotrov, Aleksey Tutin, Dmitry Lioznov, Marina Stukova

PMC · DOI: 10.3390/vaccines14010063 · Vaccines · 2026-01-04

## TL;DR

This study shows that hemodialysis patients can mount strong immune responses to influenza vaccines, similar to healthy individuals, despite their weakened immune systems.

## Contribution

The study provides empirical evidence of robust immune responses in hemodialysis patients following standard-dose influenza vaccination.

## Key findings

- Hemodialysis patients showed comparable antibody responses to healthy volunteers after influenza vaccination.
- Revaccination increased baseline antibody levels but did not change response patterns for most antigens.
- T-cell responses, including IFNγ-producing CD4+ Tem cells, were observed in vaccinated hemodialysis patients.

## Abstract

Background: Patients with end-stage renal disease (ESRD) on hemodialysis are at increased risk for severe influenza, and underlying immune dysfunction may limit vaccine-induced protection. Methods: This observational open-label study evaluated immune responses in 93 hemodialysis patients vaccinated with seasonal inactivated influenza vaccine (IIV) during the 2019–2020 (n = 22) and 2023–2024 (n = 71) seasons. Immune responses were comprehensively assessed using hemagglutination inhibition and microneutralization assays to measure antibody levels, together with flow cytometry analysis of key immune cell populations, including plasmablasts, T-follicular helper cells (Tfh), and effector memory T cells (Tem). Results: During the 2019–2020 season, antibody responses in hemodialysis patients were comparable to those in healthy volunteers in both younger (18–60 years) and older (over 60) age groups. By day 7 post-vaccination, there was a pronounced increase in activated Tfh1 cells, coinciding with a surge in plasmablasts and a rise in antigen-specific B cells. This was accompanied by a T-cell response mediated by IFNγ-producing and polyfunctional CD4+ Tem cells. In the 2023–2024 season, revaccination was associated with higher baseline antibody levels but did not alter subsequent response kinetics to A/H1N1pdm, A/H3N2, and B/Yamagata antigens. In contrast, responses to B/Victoria were higher in revaccinated patients throughout the entire observation period. Conclusions: Our findings confirm that standard-dose IIV vaccination is beneficial for hemodialysis patients, inducing robust and adequate humoral and T-cell immune responses.

## Linked entities

- **Diseases:** influenza (MONDO:0005812), end-stage renal disease (MONDO:0004375)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** ESRD (MESH:D007676), influenza (MESH:D007251)
- **Species:** H3N2 subtype (serotype) [taxon 119210], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12846267/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12846267/full.md

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Source: https://tomesphere.com/paper/PMC12846267