Anti-TNF-α antibodies improve intestinal barrier function in Crohn's disease
Abstract
BACKGROUND AND AIMS: Intestinal barrier function in Crohn's disease patients and their first degree healthy relatives is impaired. The increased intestinal permeability may result in an enhanced mucosal immune response and thereby aggravate intestinal inflammation. Humanised anti-TNF-α antibodies have been shown to be effective in the treatment of active Crohn's disease and in the treatment of entero-cutaneous fistula. The aim of the present study was to investigate the influence of anti-TNF-α antibody (infliximab) treatment on the intestinal barrier function of patients with active Crohn's disease. METHODS: The differential intestinal uptake of lactulose and mannitol was measured to quantify intestinal permeability in patients with long standing active Crohn's disease (n=17) directly before and seven days after treatment with infliximab (5 mg/kg bodyweight). In parallel, intestinal permeability was studied in a healthy control group (n=20). Serum samples were analysed with pulsed amperometric detection after separation on an anion exchange column. RESULTS: Intestinal permeability was significantly increased in all patients with Crohn's disease (L/M ratio 0.24±0.17) prior to infliximab treatment compared to the control group (L/M ratio 0.01±0.02; p-value <1×10(-7)). Treatment of patients with infliximab resulted in a marked decrease of intestinal permeability as measured by L/M ratio from 0.24±0.17 before to 0.02±0.02 (p-value <1×10(-7)) seven days after infliximab application. CONCLUSIONS: Treatment with anti-TNF-α antibodies improved impaired intestinal barrier function in patients with Crohn's disease. This effect may correlate to the well documented anti-inflammatory effect of TNF-α blockade in this intestinal disease.
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Another therapeutic approach includes blocking Th1 responses or using neutralizing antibodies such as infliximab (anti-TNF) antibody.
“Another therapeutic approach includes blocking Th1 responses or using neutralizing antibodies such as infliximab (anti-TNF) antibody.189,190”
From Regulation of Intestinal Barrier Function by Microbial Metabolites (2021) · cites this paper as [190]
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References 46 · Cited by 68
- Authors
- Noth, R., Stüber, E., Häsler, R., Nikolaus, S., Kühbacher, T., Hampe, J., Bewig, B., Schreiber, S., & Arlt, A.
- Affiliations
- University Hospital Schleswig-Holstein (DE)
- Christian-Albrechts-Universität zu Kiel (DE)
- Corresponding author
- Arlt, Alexander
- Venue
- Journal of Crohn s and Colitis
- Publisher
- Oxford University Press (OUP)
- Published
- 2012-05
- Volume
- 6
- Issue
- 4
- Pages
- 464-469
- ISSN
- 1873-9946 (ISSN-L)
- OpenAlex
- W2039312624
- Cited by
- 68
- References
- 46
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 3 · 2023: 7 · 2022: 8 · 2021: 5 · 2020: 7 · 2019: 11 · 2018: 1 · 2017: 7 · 2016: 1 · 2015: 3 · 2014: 3 · 2013: 5
- FWCI
- 1.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Crohn s and Colitis (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Exzellenzclusters Entzündungsforschung
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- Crohn's disease, intestinal barrier function
- MeSH terms
- Infliximab, Adolescent, Adult, Antibodies, Monoclonal, Chromatography, High Pressure Liquid, Crohn Disease, Female, Humans, Intestinal Absorption, Intestinal Mucosa, Intestines, Lactulose, Male, Mannitol, Middle Aged, Permeability, Tumor Necrosis Factor-alpha, Young Adult
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