Macrophage-derived IL-15 imprints peritoneal TRM-like CD8 T cells in cirrhosis and spontaneous bacterial peritonitis

Patients with decompensated cirrhosis exhibit impaired immune responses increasing the risk of spontaneous bacterial peritonitis. This study provides insight into a subset of human peritoneal CD8 T cells in patients with decompensated cirrhosis that have a long-lived and tissue-resident phenotype capable of effectively fighting recognised pathogens within a short period with the help of IL-15 produced by activated macrophages in a bystander fashion. This knowledge has the potential to improve immunomodulatory therapies aiming to enhance peritoneal immune surveillance, and by targeting TRM-like cells and/or IL-15 signalling pathways. In addition, high concentrations of soluble immune checkpoints in ascites should be considered when applying immune checkpoint inhibitors in decompensated cirrhosis.

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Publication Details

Journal
JHEP Reports
Published
2025-03-02
DOI
https://doi.org/10.1016/j.jhepr.2025.101381
Citations
2
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
1.59

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article

Macrophage-derived IL-15 imprints peritoneal TRM-like CD8 T cells in cirrhosis and spontaneous bacterial peritonitis

Sven Stengel, Karsten Große, Johanna Reißing, Michael Rooney et al.
2 citations
JHEP Reports
Immune Cell Function and Interaction
1.59
article

Macrophage-derived IL-15 imprints peritoneal TRM-like CD8 T cells in cirrhosis and spontaneous bacterial peritonitis

Sven Stengel, Karsten Große, Johanna Reißing, Michael Rooney, Tony Bruns, Yulia Alexandrowna Nevzorova, Sabine Baumgart, Raquel Benedé‐Ubieto, Stefanie Quickert, Mick Frissen, Oluwatomi Ibidapo-Obe, Hector Leal-Lassalle, Trong-Hieu Nguyen
article en
2 citations

Abstract

Patients with decompensated cirrhosis exhibit impaired immune responses increasing the risk of spontaneous bacterial peritonitis. This study provides insight into a subset of human peritoneal CD8 T cells in patients with decompensated cirrhosis that have a long-lived and tissue-resident phenotype capable of effectively fighting recognised pathogens within a short period with the help of IL-15 produced by activated macrophages in a bystander fashion. This knowledge has the potential to improve immunomodulatory therapies aiming to enhance peritoneal immune surveillance, and by targeting TRM-like cells and/or IL-15 signalling pathways. In addition, high concentrations of soluble immune checkpoints in ascites should be considered when applying immune checkpoint inhibitors in decompensated cirrhosis.

JHEP ReportsVol. 7(6)
Universidad Complutense de Madrid (ES), Instituto de Salud Carlos III (ES), Hospital General Universitario Gregorio Marañón (ES), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (ES), Jena University Hospital (DE), Friedrich Schiller University Jena (DE), RWTH Aachen University (DE)
Deutsche Forschungsgemeinschaft, Ministerio de Economía y Competitividad, RWTH Aachen University, Fundación Para La Innovación Y La Prospectiva En Salud En España, Interdisziplinäres Zentrum für Klinische Forschung, Universitätsklinikum Würzburg, Agencia Estatal de Investigación
Zero hunger
Openalex Percentile: Top 19%
Immune Cell Function and Interaction
1.59
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