Anti-interleukin-23 treatment linked to improved Clostridioides difficile infection survival
- PMID: 40114558
- PMCID: PMC11934156
- DOI: 10.1080/19490976.2025.2480195
Anti-interleukin-23 treatment linked to improved Clostridioides difficile infection survival
Abstract
Clostridioides difficile is a leading cause of healthcare-associated infection, and an unacceptably high proportion of patients with C. difficile infection die despite conventional antibiotic treatment. Host-directed immunotherapy has been proposed as an ideal treatment modality for C. difficile infection to mitigate the underlying toxin-mediated pathogenic immune response while sparing protective gut microbes. Interleukin-23 monoclonal antibody inhibitors are used extensively to control pro-inflammatory Th17 immune pathways in psoriasis and inflammatory bowel disease that are similarly important during C. difficile infection. We used a large retrospective electronic health record database to test the hypothesis that hospitalized patients with C. difficile infection who are on anti-IL-23 treatment will have improved survival compared to patients without anti-IL-23. A total of 9,301 anti-IL-23 patients had significantly lower probability of all-cause death within 30 d (0.54%) compared with 1:1 propensity-matched control patients (3.1%). IL-23 inhibition is a promising adjunct to C. difficile treatment, and further clinical trials repositioning anti-IL-23 monoclonal antibodies from psoriasis and inflammatory bowel disease to C. difficile infection are warranted.
Keywords: C. difficile infection; Clostridioides difficile; IL-23; Th17 immunity; interleukin-23; monoclonal antibody; retrospective study.
Conflict of interest statement
W. A. Petri is a consultant for TechLab Inc., a company that manufactures diagnostic tests for
Update of
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Anti-Interleukin-23 Treatment Linked to Improved Clostridioides difficile Infection Survival.medRxiv [Preprint]. 2024 Dec 5:2024.12.03.24318323. doi: 10.1101/2024.12.03.24318323. medRxiv. 2024. Update in: Gut Microbes. 2025 Dec;17(1):2480195. doi: 10.1080/19490976.2025.2480195. PMID: 39677433 Free PMC article. Updated. Preprint.
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