Decrease in Mucosal IL17A, IFNγ and IL10 Expressions in Active Crohn's Disease Patients Treated with High-Dose Vitamin Alone or Combined with Infliximab

Nutrients. 2020 Nov 30;12(12):3699. doi: 10.3390/nu12123699.

Abstract

Background: Vitamin D treatment may reduce Crohn's disease (CD) activity by modulating the mucosal immune function. We investigated if high-dose vitamin D +/- infliximab modulated the mucosal cytokine expression in active CD.

Methods: Forty CD patients were randomized into: infliximab + vitamin D; infliximab + placebo-vitamin D; placebo-infliximab + vitamin D or placebo-infliximab + placebo-vitamin D. Infliximab (5 mg/kg) and placebo-infliximab were administered at weeks 0, 2 and 6. Oral vitamin D was administered as bolus 200,000 international units (IU) per week 0 followed by 20,000 IU/day for 7 weeks or placebo. Endoscopy with biopsies was performed at weeks 0 and 7 where endoscopic activity was measured and mucosal mRNA cytokine expression was examined. C-reactive protein (CRP), fecal calprotectin and Harvey-Bradshaw Index (HBI) were measured at weeks 0, 2 and 6.

Results: High-dose vitamin D treatment alone and combined with infliximab decreased the IL17A, IFNγ and IL10 expression. High-dose vitamin D alone did not significantly decrease the disease activity, CRP or calprotectin. Combined infliximab and vitamin D treatment was not clinically significantly superior to monotherapy with infliximab.

Conclusions: High-dose vitamin D as monotherapy and combined with infliximab decreases IL17A, IFNγ and IL-10 expression in mucosa within treatment groups. This did not induce a statistically significant decreased disease activity. EudraCT no.2013-000971-34.

Keywords: Crohn’s disease; infliximab; vitamin D treatment.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • C-Reactive Protein / metabolism
  • Crohn Disease
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Gene Expression Regulation
  • Humans
  • Infliximab / therapeutic use*
  • Interferon-gamma / genetics*
  • Interferon-gamma / metabolism
  • Interleukin-10 / genetics*
  • Interleukin-10 / metabolism
  • Interleukin-17 / genetics*
  • Interleukin-17 / metabolism
  • Leukocyte L1 Antigen Complex / genetics
  • Leukocyte L1 Antigen Complex / metabolism
  • Middle Aged
  • Mucous Membrane / drug effects*
  • Mucous Membrane / metabolism
  • Vitamin D / therapeutic use
  • Vitamins
  • Young Adult

Substances

  • IL10 protein, human
  • IL17A protein, human
  • Interleukin-17
  • Leukocyte L1 Antigen Complex
  • Vitamins
  • Interleukin-10
  • Vitamin D
  • Interferon-gamma
  • C-Reactive Protein
  • Infliximab