Intestinal fibrosis is associated with lack of response to Infliximab therapy in Crohn's disease

PLoS One. 2018 Jan 24;13(1):e0190999. doi: 10.1371/journal.pone.0190999. eCollection 2018.

Abstract

Introduction: Overt fibrostenotic disease is a relative contraindication for anti-TNF therapy in Crohn's disease. We hypothesized that subclinical fibrosis may also contribute to an incomplete response to anti-TNF therapy before the onset of symptomatic stenosis.

Methods: In a previous trial, patients with ileocecal Crohn's disease were randomized to either immediate ileocecal resection or medical treatment with Infliximab. In case of insufficient response to Infliximab, the latter underwent secondary ileocecal resection. We compared specimens from those patients undergoing immediate resection (Infliximab naïve, n = 20) to those who failed Infliximab therapy (n = 20).

Results: Infliximab naïve and Infliximab failure patients had similar severity of inflammation when assessed by CRP levels (median 14 vs 9 mg/L) and histology (Geboes-D'Haens-score, median 10 vs 11 points). On immunohistochemistry, collagen-III and fibronectin depositions were increased in patients previously exposed to Infliximab compared to patients naïve to Infliximab. On mRNA level, procollagen peptidase showed significantly more mucosal mRNA expression in Crohn's disease patients who failed Infliximab. Infliximab responders showed no increase of this marker after 4 weeks of successful Infliximab treatment.

Discussion: Failure to Infliximab therapy is associated with subclinical fibrosis in Crohn's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Crohn Disease / complications
  • Crohn Disease / drug therapy*
  • Crohn Disease / metabolism
  • Extracellular Matrix Proteins / metabolism
  • Female
  • Fibrosis
  • Gastrointestinal Agents / therapeutic use*
  • Humans
  • Infliximab / therapeutic use*
  • Intestinal Diseases / complications*
  • Intestinal Diseases / metabolism
  • Intestinal Diseases / pathology
  • Intestinal Mucosa / enzymology
  • Male
  • Middle Aged
  • Procollagen N-Endopeptidase / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Young Adult

Substances

  • Extracellular Matrix Proteins
  • Gastrointestinal Agents
  • Infliximab
  • Procollagen N-Endopeptidase

Grants and funding

This research was fully granted by institutional funding from the Academic Medical Center, Amsterdam, the Netherlands. No extramural funding was received.