# Role of γδ T cells in turkey herpesvirus vaccine protection against Marek’s disease virus

**Authors:** Mohammad A. Sabsabi, Ahmed Kheimar, Dominik von La Roche, Sonja Härtle, Dusan Kunec, Yulin Cong, Lisa Kossak, Theresa von Heyl, Benjamin Schusser, Benedikt B. Kaufer

PMC · DOI: 10.1099/jgv.0.002204 · 2026-01-30

## TL;DR

This study shows that γδ T cells have a minor role in vaccine protection against a deadly chicken virus but greatly affect virus shedding.

## Contribution

The study reveals the limited role of γδ T cells in turkey herpesvirus vaccine protection and their significant impact on virus shedding.

## Key findings

- γδ T-cell-knockout chickens showed increased disease incidence after vaccination and MDV challenge.
- Viral load in the spleen, skin, and dust was significantly higher in γδ T-cell-knockout chickens.
- γδ T cells appear to have a minor role in vaccine protection but a major role in controlling virus shedding.

## Abstract

γδ T cells are a highly abundant lymphocyte subset in chickens and play key roles in early immune responses to infection. It has been recently shown that γδ T cells restrict Marek’s disease virus (MDV) pathogenesis; however, it remained elusive if they play a role in vaccine protection. In this study, we vaccinated γδ T-cell-knockout chickens with the commercial turkey herpesvirus (HVT) vaccine and challenged them with very virulent MDV. The disease incidence was significantly increased in vaccinated chickens in the absence of γδ T cells. This increase was comparable to a previous study in unvaccinated γδ T-cell-knockout chickens, suggesting that γδ T cells only play a minor role in vaccine protection. Furthermore, the viral load in the spleen was significantly increased in the absence of γδ T cells. Interestingly, viral load in the skin and in dust shed by the animals was drastically increased, suggesting that the absence of γδ T cells affects MDV shedding. In addition, we quantified various immune cell subsets to determine if these could be responsible for the observed phenotypes. Together, our data indicate that γδ T cells only play a minor role in HVT-mediated protection, but their absence drastically affects shedding of this deadly pathogen in vaccinated animals.

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 395362], NOS2 (nitric oxide synthase 2) [NCBI Gene 395807] {aka INOS, NOS2A}, CD8A (CD8A molecule) [NCBI Gene 403158] {aka CD8, CD8-alpha}
- **Diseases:** infection (MESH:D007239), T-cell lymphomas (MESH:D016399), Tumour (MESH:D009369), lymphomas (MESH:D008223), neurological disorders (MESH:D009461), MDV (MESH:D008380), diarrhoea (MESH:D003967)
- **Chemicals:** nitrogen (MESH:D009584), SB-1 (MESH:C047101), CVI988 (-), streptomycin (MESH:D013307), penicillin (MESH:D010406), chloroform (MESH:D002725), PAN (MESH:C041728), phenol (MESH:D019800), CO2 (MESH:D002245)
- **Species:** herpesvirus [taxon 39059], Gallid alphaherpesvirus 2 (Marek disease virus type 1, no rank) [taxon 10390], Newcastle disease virus [taxon 11176], Gallus gallus (bantam, species) [taxon 9031], Meleagrid alphaherpesvirus 1 (herpesvirus of turkeys, no rank) [taxon 37108], Gallid alphaherpesvirus 1 (no rank) [taxon 10386], unidentified influenza virus (species) [taxon 11309], Infectious bursal disease virus (Gumboro virus, no rank) [taxon 10995], Clostridium perfringens (species) [taxon 1502]
- **Cell lines:** RB-1B — Homo sapiens (Human), Retinoblastoma, Induced pluripotent stem cell (CVCL_VE63)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12859218/full.md

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Source: https://tomesphere.com/paper/PMC12859218