# An mRNA influenza vaccine induces immunity comparable to an adjuvanted vaccine in a randomized trial

**Authors:** Carole Henry, Daniel Makrinos, Runxia Liu, Maria Cavallaro, Brooke Fenderson, Yanbo Sun, Xiaolin Chang, Eleanor Astley, Bethany Girard, Wen-Han Yu, Jaap Oostendorp, Anthony DiPiazza, Robert Paris

PMC · DOI: 10.1038/s41541-026-01370-7 · NPJ Vaccines · 2026-01-14

## TL;DR

An mRNA influenza vaccine was found to induce immune responses comparable to a licensed adjuvanted vaccine in a clinical trial.

## Contribution

The study demonstrates the immunogenicity of an mRNA-based influenza vaccine compared to a standard adjuvanted vaccine.

## Key findings

- Both vaccines elicited durable hemagglutination inhibition titers and increased HA-specific memory B cell responses.
- mRNA-1010 induced higher frequencies of classical and activated MBCs specific to the H3 HA strain compared to FLUAD.
- mRNA-1010 and FLUAD generated strong CD4+ T-cell responses, with a trend toward higher CD8+ T-cell responses in mRNA-1010 recipients.

## Abstract

Influenza causes substantial morbidity and mortality worldwide. This randomized, open-label, phase 1 trial (ClinicalTrials.gov, NCT05397223, date of registration: May 31, 2022) compared the immunogenicity of an mRNA-based quadrivalent influenza hemagglutinin (HA) vaccine (mRNA-1010) with a licensed comparator (FLUAD) in adults aged 18-75 years. We evaluated humoral and cellular immune responses using hemagglutination inhibition assays, flow cytometry-based memory B cell (MBC) profiling, and intracellular cytokine staining for T-cell characterization. Both vaccines elicited durable hemagglutination inhibition titers and increased HA-specific MBC responses across four vaccine strains. Compared with FLUAD, mRNA-1010 induced higher frequencies of classical and activated MBCs specific to the H3 HA included in the vaccine, while inducing similar MBC responses to the other strains. mRNA-1010 and FLUAD generated strong HA-specific CD4+ T-cell responses; a trend toward higher CD8+ T-cell responses was observed in mRNA-1010 recipients compared with FLUAD recipients for two of the four strains. These findings support the potential of the mRNA platform for seasonal influenza vaccination.

## Linked entities

- **Proteins:** CD4 (CD4 molecule), CD8A (CD8 subunit alpha)
- **Diseases:** influenza (MONDO:0005812)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** Influenza (MESH:D007251)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12901179/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12901179/full.md

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Source: https://tomesphere.com/paper/PMC12901179