# Neutrophils negatively control IL-17A-producing γδ T cell frequencies in a contact-dependent manner under physiological conditions

**Authors:** Xinhua Yu, Xiaoyang Yue, Junie D. Tchudjin Magatsin, Sebastian Marwitz, Jochen Behrends, Torsten Goldmann, Joseph T. Opferman, Brigitte Kasper, Frank Petersen

PMC · DOI: 10.3389/fimmu.2025.1542191 · Frontiers in Immunology · 2025-03-20

## TL;DR

Neutrophils reduce the number of IL-17A-producing γδ T cells through direct contact, helping maintain immune balance in healthy conditions.

## Contribution

This study reveals a novel physiological role of neutrophils in negatively regulating IL-17A-producing γδ T cells via direct cell contact.

## Key findings

- Neutrophils inhibit IL-17A-producing γδ T cells by inducing cell death in a contact-dependent manner.
- γδ T cells in neutropenic mice show unique gene expression profiles and accumulate in cervical lymph nodes.
- The interaction between neutrophils and γδ T cells is crucial for immune homeostasis under physiological conditions.

## Abstract

In addition to serving as the primary effector cells against infections, neutrophils have been implicated in the regulation of both innate and adaptive immunity. In this study, we aimed to investigate the role of neutrophils in the regulation of the immune system under physiological conditions.

The in vivo effect of neutrophils on the immune system was examined using neutropenic mice. The interaction between neutrophils and γδ T cells was investigated using an in vitro co-culture system.

Unexpectedly, we observed an accumulation of γδ T cells in the cervical lymph nodes of neutropenic mice. Transcriptomic analysis revealed that these γδ T cells exhibited unique expression profiles of cell surface molecules and genes involved in defense responses. Further characterization indicated that the accumulated γδ T cells were IL-17 producing CD44+CD62L−CD27− memory cells. Additionally, in vitro experiments demonstrated that neutrophils could inhibit the function of IL-17A producing γδ T cells by inducing cell death in a contact-dependent manner.

This present study demonstrates that neutrophils negatively regulate IL-17 producing γδ T cells under physiological conditions. Given that IL-17A is a critical cytokine for the recruitment of neutrophils to peripheral tissues, our study suggests that the crosstalk between neutrophils and IL-17A producing γδ T cells is a crucial mechanism for maintaining immune homeostasis under physiological conditions.

## Linked entities

- **Proteins:** IL17A (interleukin 17A)

## Full-text entities

- **Genes:** Sell (selectin, lymphocyte) [NCBI Gene 20343] {aka CD62L, L-selectin, LAM-1, LECAM-1, LECAM1, Lnhr}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Cd44 (CD44 antigen) [NCBI Gene 12505] {aka HERMES, Ly-24, Pgp-1}, Cd27 (CD27 antigen) [NCBI Gene 21940] {aka S152, Tnfrsf7, Tp55}
- **Diseases:** neutropenic (MESH:D044504)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11965643/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC11965643/full.md

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Source: https://tomesphere.com/paper/PMC11965643