Aim: the main aim of this study is to investigate if immune cells (regulatory T-cells, Th17 cells and other immune cell types) or biomarkers can be used to predict the response or lack of response to treatment with Infliximab. If so, characteristics of the immune cells may also unveil the mechanisms behind lack of response to Infliximab. Design: a prospective, observational study with three arms. In the treatment group, 35 patients with Crohn's disease about to start Infliximab-treatment are recruited. They have blood samples drawn at day 1 before first treatment, after 6 week, and again after 22 weeks of treatment. 12 healthy volunteers serve as a control group. Controls are only investigated once. All treatment and follow-up are according to national guidelines, and data from this study is not used by the clinicians. Methods: the number of regulatory T-cells and pro-inflammatory T-cells (Th17 cells) is investigated using flow cytometry. From plasma and serum samples, various proteins (biomarkers), such as transforming growth factor beta (TGF-beta) and tumour necrosis factor alpha (TNF-alpha), are measured using immunoassays. Patient data (demographics and medical history) are extracted from various registries.
Primary analyses: patient response to Infliximab treatment is quantified using Harvey Bradshaw Index, and the response is then related to the number of regulatory T-cells, Th17 cells, and biomarker levels at baseline. The exact cut-off for response vs. non-respons will be determined and validated once all data is collected by an assessor blinded for the flow cytometry results and biomarker levels. Plan for missing data: for patients with missing Harvey Bradshaw Index, we will first try to re-create the score using the patient records (information on well-being, abdominal pain, diarrhea, fistulae/abscesses, and extra-intestinal Crohn manifestations). If this is not possible, an experienced clinician will rate the patient's Infliximab response based on all available patient record data, but blinded for flow cytometry results and biomarker levels.
Study Type
OBSERVATIONAL
Enrollment
47
The patients are included in the study when the decision to treat with Infliximab is already made. This study is observational, and all treatment and clinical follow-up are according to national guidelines.
Hvidovre Hospital
Hvidovre, Copenhagen, Denmark
Change from baseline in number of regulatory T-cells at 6 weeks
The number of regulatory T-cells is measured in fresh blood by flow cytometry.
Time frame: Baseline, 6 weeks (plus/minus 1 week)
Change from baseline in number of regulatory T-cells at 22 weeks
The number of regulatory T-cells is measured in fresh blood by flow cytometry.
Time frame: Baseline, 22 weeks (plus/minus 1 week)
Change from baseline in Harvey Bradshaw Index at 6 weeks
Harvey Bradshaw Index is a measure of Crohn's Disease severity.
Time frame: Baseline, 6 weeks (plus/minus 1 week)
Change from baseline in CD161 expression at 6 weeks
Cluster of differentiation 161 (CD161) is a T helper 17 cell (Th17)-marker, measured by flow cytometry of fresh blood samples.
Time frame: Baseline, 6 weeks (plus/minus 1 week)
Change from baseline in CD161 expression at 22 weeks
CD161 is a Th17-marker, measured by flow cytometry of fresh blood samples.
Time frame: Baseline, 22 weeks (plus/minus 1 week)
Change from baseline in cytokine levels at 6 weeks
We will measure IFN-gamma, IL-4, IL-6, IL-7, IL-10, IL-15, IL-17, and TNF-alpha by Luminex. TGF-beta, suPAR, and IL-15 will be measured by ELISA.
Time frame: Baseline, 6 weeks (plus/minus 1 week)
Change from baseline in cytokine levels at 22 weeks
We will measure IFN-gamma, IL-4, IL-6, IL-7, IL-10, IL-15, IL-17, and TNF-alpha by Luminex. TGF-beta, suPAR, and IL-15 will be measured by ELISA.
Time frame: Baseline, 22 weeks (plus/minus 1 week)
Change from baseline in Harvey Bradshaw Index at 22 weeks
Harvey Bradshaw Index is a measure of Crohn's Disease severity.
Time frame: Baseline, 22 weeks (plus/minus 1 week)
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