The expression IL1B correlates negatively with the clinical response to adalimumab in Crohn's disease patients: An ex vivo approach using peripheral blood mononuclear cells.

Anti-TNFα therapy Crohn's disease In vitro inflammation In vitro monocyte to macrophage differentiation Inflammatory cytokines Personalized medicine

Journal

Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521

Informations de publication

Date de publication:
01 Aug 2023
Historique:
received: 27 02 2023
revised: 07 05 2023
accepted: 25 05 2023
medline: 16 6 2023
pubmed: 1 6 2023
entrez: 31 5 2023
Statut: ppublish

Résumé

Understanding of the molecular mechanisms of anti-TNFα therapy non-response and reliable biomarkers are essential for personalized medicine in Crohn's disease (CD) patients. Using RNA-seq data adjusted for deconvoluted fractions of peripheral blood cells, we recently described MMD gene, coding for a monocyte to macrophage differentiation factor, as a biomarker of adalimumab (anti-TNFα) therapy response in CD. The results also suggest that cell subtype-specific biomarkers may be superior to those measured in bulk peripheral blood. Here, we used functional cell model to further investigate the role of the monocyte to macrophage differentiation in adalimumab treatment response and evaluate monocyte/macrophage specific expression of the inflammatory cytokines as potential biomarkers for (non)response to adalimumab in CD patients. The peripheral monocytes of CD patients responsive and non-responsive to adalimumab were isolated, differentiated into macrophages, and exposed to inflammation and concurrent adalimumab therapy in vitro. The results were correlated to the clinical response of the donor patients. Correlation is shown of the expression of two macrophage differentiation related genes- CD68 and MMD, with the expression of the inflammatory cytokines TNF, IL1B, IL6 and CXCL8. Monocytes and in vitro differentiated macrophages of adalimumab non-responders express more inflammatory cytokines than those of responders. The biggest difference was in the IL1B expression. Additionally, IL1B expression in the in vitro differentiated macrophages of CD patients correlates negatively with their clinical response to adalimumab. We propose the IL1B expression in the macrophages as a possible biomarker for adalimumab response in CD patients.

Identifiants

pubmed: 37257580
pii: S0024-3205(23)00456-3
doi: 10.1016/j.lfs.2023.121822
pii:
doi:

Substances chimiques

Adalimumab FYS6T7F842
Cytokines 0
Biomarkers 0
IL1B protein, human 0
Interleukin-1beta 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

121822

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest.

Auteurs

Boris Gole (B)

University of Maribor, Faculty of Medicine, Centre for Human Molecular Genetics and Pharmacogenomics, Taborska ulica 8, SI-2000 Maribor, Slovenia.

Cvetka Pernat (C)

Maribor University Medical Centre, Division of Internal Medicine, Department of Gastroenterology, Ljubljanska ulica 5, SI-2000 Maribor, Slovenia.

Gregor Jezernik (G)

University of Maribor, Faculty of Medicine, Centre for Human Molecular Genetics and Pharmacogenomics, Taborska ulica 8, SI-2000 Maribor, Slovenia.

Uroš Potočnik (U)

University of Maribor, Faculty of Medicine, Centre for Human Molecular Genetics and Pharmacogenomics, Taborska ulica 8, SI-2000 Maribor, Slovenia; University of Maribor, Faculty of Chemistry and Chemical Engineering, Laboratory for Biochemistry, Molecular Biology and Genomics, Smetanova ulica 17, SI-2000 Maribor, Slovenia. Electronic address: uros.potocnik@um.si.

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Classifications MeSH