Decoding cytokine networks in ulcerative colitis to identify pathogenic mechanisms and therapeutic targets

Ulcerative colitis (UC) is a chronic inflammatory disorder of the gastrointestinal tract that is characterized by dysregulated cytokine signaling. Treatment outcomes for patients with UC remain suboptimal despite the advent of cytokine-targeting therapies, necessitating a better understanding of the interconnected cytokine signaling networks that are perturbed in patients with UC. To address this, we undertook systems immunology modeling of single-cell transcriptomics data from colonic biopsies of treatment-naive and treatment-exposed patients with UC to build complex cytokine signaling networks underpinned by putative cytokine-cytokine interactions. The generated cytokine networks effectively captured known, physiologically relevant cytokine-cytokine interactions, which we validated in vitro in colonic epithelial organoids derived from patients with UC and with organoids cocultured with innate lymphoid cells. These networks revealed several previously unrecognized aspects of UC pathogenesis. These included the identification of a cytokine subnetwork that is unique to treatment-naive patients with UC, of cytokines with altered interaction patterns across UC disease states (including IL-22, TL1A, IL-23A, and OSM), and of cytokine-cytokine interactions that were mediated by specific members of the Janus-associated kinase (JAK) family. In particular, our network analysis positioned TL1A as an important upstream regulator of TNF and IL-23A (both of which are targeted by approved UC drugs) and suggested it as a potential therapeutic target. Together, these findings open several avenues for guiding future cytokine-targeting therapeutic approaches in UC, and the presented methodology can be readily applied to gain similar insights into other immune-mediated inflammatory diseases.

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Publication Details

Journal
Science Signaling
Published
2026-02-03
DOI
https://doi.org/10.1126/scisignal.adt0986
Primary Topic
Inflammatory Bowel Disease
Type
article
Field-Weighted Citation Impact
0.00

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article

Decoding cytokine networks in ulcerative colitis to identify pathogenic mechanisms and therapeutic targets

Isabelle Hautefort, Balázs Bohár, Diana Coman, Márton Ölbei et al.
Science Signaling
Inflammatory Bowel Disease
article

Decoding cytokine networks in ulcerative colitis to identify pathogenic mechanisms and therapeutic targets

Isabelle Hautefort, Balázs Bohár, Diana Coman, Márton Ölbei, Luca Csabai, Hajir Ibraheim, Dezső Módos, Joana F. Neves, Sandra Koigi, Emma Højmose Kromann, John P. Thomas, Nick Powell, Diana Papp, Tamas Korcsmaros
article en

Abstract

Ulcerative colitis (UC) is a chronic inflammatory disorder of the gastrointestinal tract that is characterized by dysregulated cytokine signaling. Treatment outcomes for patients with UC remain suboptimal despite the advent of cytokine-targeting therapies, necessitating a better understanding of the interconnected cytokine signaling networks that are perturbed in patients with UC. To address this, we undertook systems immunology modeling of single-cell transcriptomics data from colonic biopsies of treatment-naive and treatment-exposed patients with UC to build complex cytokine signaling networks underpinned by putative cytokine-cytokine interactions. The generated cytokine networks effectively captured known, physiologically relevant cytokine-cytokine interactions, which we validated in vitro in colonic epithelial organoids derived from patients with UC and with organoids cocultured with innate lymphoid cells. These networks revealed several previously unrecognized aspects of UC pathogenesis. These included the identification of a cytokine subnetwork that is unique to treatment-naive patients with UC, of cytokines with altered interaction patterns across UC disease states (including IL-22, TL1A, IL-23A, and OSM), and of cytokine-cytokine interactions that were mediated by specific members of the Janus-associated kinase (JAK) family. In particular, our network analysis positioned TL1A as an important upstream regulator of TNF and IL-23A (both of which are targeted by approved UC drugs) and suggested it as a potential therapeutic target. Together, these findings open several avenues for guiding future cytokine-targeting therapeutic approaches in UC, and the presented methodology can be readily applied to gain similar insights into other immune-mediated inflammatory diseases.

Science SignalingVol. 19(923)
Eötvös Loránd University (HU), King's College London (GB), Hammersmith Hospital (GB), Quadram Institute (GB), Earlham Institute (GB), NIHR Imperial Biomedical Research Centre (GB), Imperial College London (GB)
Bristol-Myers Squibb, Eli Lilly and Company, Pfizer, Stanford University, Celgene, Leona M. and Harry B. Helmsley Charitable Trust, Wellcome Trust, UK Research and Innovation, National Institute for Health and Care Research, Leverhulme Trust, Department of Health and Social Care, Imperial College London, King's College London, Lister Institute of Preventive Medicine, Koninklijke Nederlandse Akademie van Wetenschappen, Vifor Pharma, Allergan, Medical Research Council, Biotechnology and Biological Sciences Research Council, NIHR Imperial Biomedical Research Centre
Good health and well-being
Openalex Percentile: Top 65%
Inflammatory Bowel Disease
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