Redefining the role of IL-18 in post-surgical recovery and sepsis: a key mediator of inflammation resolution
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F25%3A00082413" target="_blank" >RIV/00159816:_____/25:00082413 - isvavai.cz</a>
Result on the web
<a href="https://link.springer.com/article/10.1186/s12967-025-06652-7" target="_blank" >https://link.springer.com/article/10.1186/s12967-025-06652-7</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1186/s12967-025-06652-7" target="_blank" >10.1186/s12967-025-06652-7</a>
Alternative languages
Result language
angličtina
Original language name
Redefining the role of IL-18 in post-surgical recovery and sepsis: a key mediator of inflammation resolution
Original language description
BackgroundTimely resolution of innate immune responses activated by surgical intervention is crucial for patient recovery. While cytokines and innate immune cells are critical in inflammation resolution, the specific role of IL-18 in these processes remains controversial and underexplored.MethodsWe investigate determinants of successful recovery using peripheral blood samples from orthopedic surgery (ORT) patients (n = 33) at T0 (before surgery), T1 (24 h after surgery) and T2 (3 days after surgery). Monocytes from ORT patients underwent immunophenotyping together with bulk transcriptomic analysis. We found that IL-18 strongly defines the recovery immune signature. These results were further validated in vitro by comparing IL-18 and TNF-alpha effects on monocytes, and in 3D human intestine organoids together with single cell (sc)-RNAseq analysis.ResultsTranscriptomics of ORT monocytes revealed upregulation of ITG family integrins, namely ITGB3 and ITGB5, CXCL family chemokines, notably CXCL1-3, CXCL5, and SCL/TAL1 factor controlling differentiation and migration, but not pro-inflammatory genes. Similar changes were observed in IL-18 stimulated healthy donor monocytes in vitro, including an increase in CD11b, CD64, and CD86 levels, accompanied by increased phosphorylation of Akt but not NF kappa B. These changes were attenuated in the presence of TNF-alpha, thus showing a unique role of IL-18 when acting alone without its most frequent paired cytokine TNF-alpha. We further confirmed that IL-18 induces monocyte-macrophage transition and migration using human intestinal organoids. Finally, TNF-alpha/IL-18 ratio showed a high predictive value of clinical severity in septic patients.ConclusionsWe propose a novel role of IL-18 on monocyte migration and macrophage transition characterizing successful orthopedic surgery recovery, as well as the ratio of IL-18/TNF-alpha as a novel marker of inflammation resolution, with potential implications for patient monitoring and therapeutic strategies.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30102 - Immunology
Result continuities
Project
<a href="/en/project/NU21-06-00408" target="_blank" >NU21-06-00408: Predictive potential of dynamic changes in neutrophil and monocyte subsets in SIRS and sepsis development after surgery or trauma.</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2025
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of translational medicine
ISSN
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e-ISSN
1479-5876
Volume of the periodical
23
Issue of the periodical within the volume
1
Country of publishing house
GB - UNITED KINGDOM
Number of pages
22
Pages from-to
728
UT code for WoS article
001522052500004
EID of the result in the Scopus database
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