Emerging therapeutic targets and strategies in Crohn's disease

Expert Rev Gastroenterol Hepatol. 2016 Jun;10(6):735-44. doi: 10.1586/17474124.2016.1142372. Epub 2016 Feb 16.

Abstract

Crohn's disease (CD) is an immune-mediated inflammatory bowel disease, in which inflammation is driven by a complex interaction between the microbiota, immune cells, genes and mediators. New mechanisms of action and several cytokines have been identified as factors involved in the inflammatory process in CD, and many new molecules have been developed to treat this complex disease. New agents have been developed that target leukocyte trafficking, block or adhesion molecules for example, as well as the development of antibodies against classic inflammatory cytokines or therapies directed against IL-12/23 and Janus kinases. The development of selective mechanisms of action and targeting of different cytokines or inflammatory mediators for each patient presents the biggest challenge for the future in CD therapy. Such agents are currently at different phases of development. We aim to review the current literature data on a targeted approach in CD, which could be promising alternative approach for CD patients in the near future.

Keywords: Crohn’s disease; anti-adhesion molecules; anti-cytokine; biologics; small molecules.

Publication types

  • Review

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / adverse effects
  • Anti-Inflammatory Agents / therapeutic use*
  • Cell Adhesion Molecules / antagonists & inhibitors*
  • Cell Adhesion Molecules / immunology
  • Chemotaxis, Leukocyte / drug effects
  • Crohn Disease / diagnosis
  • Crohn Disease / drug therapy*
  • Crohn Disease / immunology
  • Gastrointestinal Agents / adverse effects
  • Gastrointestinal Agents / therapeutic use*
  • Humans
  • Inflammation Mediators / antagonists & inhibitors*
  • Inflammation Mediators / immunology
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / pathology
  • Molecular Targeted Therapy* / adverse effects
  • Signal Transduction / drug effects
  • Treatment Outcome

Substances

  • Anti-Inflammatory Agents
  • Cell Adhesion Molecules
  • Gastrointestinal Agents
  • Inflammation Mediators