# Preconditioning donors with corticosteroids improves early lung graft immunity

**Authors:** Isabelle Schwartz-Cornil, Florentina Pascale, Luc Jouneau, Maxime Huriet, Jérôme Estephan, Mickael Bourge, Christophe Richard, Valérie Gelin, Claudia Bevilacqua, Julie Rivière, Thien-Phong Vu Manh, Maxime Djebbour, Antoine Premachandra, Carla Gouin, Julien De Wolf, Chloé Mimbimi, Antoine Magnan, Antoine Roux, Stanislas Grassin-Delyle, Philippe Devillier, Delphyne Descamps, Nicolas Bertho, Sébastien Jacqmin, Morgan Le Guen, Edouard Sage, Matthieu Glorion

PMC · DOI: 10.3389/fimmu.2025.1668591 · Frontiers in Immunology · 2025-10-28

## TL;DR

Giving corticosteroids to organ donors improves the early immune response in transplanted lungs, reducing T-cell infiltration and promoting anti-inflammatory effects.

## Contribution

This study provides new evidence that donor corticosteroid treatment improves lung graft immunity through macrophage-targeted mechanisms.

## Key findings

- Donor corticosteroid treatment reduced CD3pos T-cell infiltration in lung grafts.
- Corticosteroids enhanced the anti-inflammatory profile of alveolar macrophages.
- T-cell-attracting chemokine expression was reduced in corticosteroid-treated lungs.

## Abstract

Preclinical studies have recently revealed the critical role of innate immunity in determining lung transplantation outcomes. Although the International Society for Heart and Lung Transplantation recommends high-dose corticosteroid administration to donors, this practice is inconsistently applied worldwide. Investigating its impact on the donor lung’s innate immune response – an unexplored area - could provide valuable evidence to support adoption of donor preconditioning with corticosteroids, beyond their traditional administration to recipients.

We used a cross-circulatory pig platform that consists of a donor lung placed extracorporeally and connected to the circulation of a recipient pig whose leukocytes are fluorescently labeled.

Donor preconditioning - compared to recipient’s treatment alone - reduced the presence of CD3pos T-cells in the graft from both the donor and recipient, and enhanced the anti-inflammatory profile of alveolar macrophages, at least during the first 10 hours of donor-recipient interaction. The alveolar macrophages isolated from corticosteroid-preconditioned pig lungs exhibited decreased gene expression of T-cell-attracting chemokines during the 10-hour reperfusion period, correlating with the reduced T-cell infiltration. Similarly, human lung macrophages showed lower expression of these T-cell-attracting chemokines and higher anti-inflammatory profiles with corticosteroid treatment.

Our results show that the early immune status of lung grafts is improved by treating donors with corticosteroids through macrophage-targeted mechanisms. This finding provides an immunological rationale for expanding the implementation of donor preconditioning with corticosteroids.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12602223/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12602223/full.md

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Source: https://tomesphere.com/paper/PMC12602223