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Risk of serious infections in patients with inflammatory bowel disease treated with biologic and small molecule therapies: A nationwide cohort study
Division of Gastroenterology, Department of Medicine, NYU Grossman School of Medicine, New York, USA.
Division of Clinical Epidemiology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Gastroenterology Unit, Department of Gastroenterology, Dermatovenereology and Rheumatology, Karolinska University Hospital, Stockholm, Sweden.
Division of Clinical Epidemiology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg, Sweden; Department of Pediatrics, Queen Silvia Children's Hospital, Gothenburg, Sweden.
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2026 (English)In: Journal of Crohn's & Colitis, ISSN 1873-9946, E-ISSN 1876-4479, Vol. 20, no 2, article id jjaf229Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: We aimed to assess the risk of serious infections in patients with inflammatory bowel disease (IBD) exposed to different advanced therapies.

METHODS: We linked nationwide registers and compared rates of incident serious infections in patients with Crohn's disease (CD) and ulcerative colitis (UC) exposed to medical therapies versus matched general population comparators during 2007 to 2023. We 1:1 propensity score-matched individuals with IBD to compare infection risk across therapies.

RESULTS: We identified 55,866 patients with IBD naïve to immunomodulators (IMM) and advanced therapies, 20,392 exposed to IMM, 15,973 to anti-TNF, 9035 to IMM with anti-TNF, 3948 to vedolizumab, 2926 to ustekinumab, 659 to tofacitinib, 987 to upadacitinib, 262 to filgotinib, and 163 to risankizumab with 987,366 matched comparators with up to 18 years of follow-up. Compared to the general population [incidence rate range 0.39-1.13 per 100 person-years (PY)], patients with IBD had a higher incidence of serious infections [naïve 2.31 per 100 PY; adjusted hazard ratio (aHR) 1.89, 95% Confidence Interval (CI) 1.84-1.94], IMM 3.27 per 100 PY (aHR 4.45 95% CI 4.24-4.66), advanced therapies range 3.14-8.10 per 100 PY (aHRs range 3.45-10.55, 95% CI range 3.04-26.65). Relative risks were elevated in the pediatric population, and for opportunistic and gastrointestinal infections. No differences in infection rates were observed in propensity score-matched comparisons of different advanced therapies.

CONCLUSION: Patients with IBD were at an increased risk of infections, even among those naïve to IMM and advanced therapies. There was no significant difference in risk of infections across advanced therapy exposures.

Place, publisher, year, edition, pages
Oxford University Press, 2026. Vol. 20, no 2, article id jjaf229
Keywords [en]
advanced therapies, anti-tumor necrosis factor-alpha, opportunistic infection, risankizumab, tofacitinib, upadacitinib, ustekinumab, vedolizumab
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-125871DOI: 10.1093/ecco-jcc/jjaf229ISI: 001690856100001PubMedID: 41397902OAI: oai:DiVA.org:oru-125871DiVA, id: diva2:2023812
Funder
Swedish Research Council, 2020-02002Region Stockholm, FoUI-1002495Karolinska Institute, FoUI-1002495
Note

Funding Agencies:

This project was supported by grants from the Swedish Research Council (Dnr 2020-02002)and the Regional Agreement on Medical Training and Clinical Research between StockholmCounty Council and Karolinska Institutet (ALF Dnr FoUI-1002495). 

Available from: 2025-12-22 Created: 2025-12-22 Last updated: 2026-02-26Bibliographically approved

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Halfvarson, JonasLudvigsson, Jonas F.

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