Table of Contents Author Guidelines Submit a Manuscript
Gastroenterology Research and Practice
Volume 2011 (2011), Article ID 287574, 10 pages
Review Article

Biologics in Paediatric Crohn's Disease

1Department of Paediatrics, Monash University, Clayton, VIC 3800, Australia
2Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville Melbourne, VIC 3052, Australia
3Gut and Liver Group, Murdoch Childrens Research Institute, Parkville, VIC 3052, Australia
4Department of Paediatrics, University of Melbourne, Melbourne, VIC 3052, Australia

Received 25 April 2011; Revised 10 July 2011; Accepted 1 October 2011

Academic Editor: Peter M. Irving

Copyright © 2011 Oliver Gouldthorpe et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Crohn's disease affects increasing numbers of children worldwide. Generally, childhood-onset disease runs a more severe course than in adults and has a greater impact on quality of life. Therapy in children must take account of a different set of risks for toxicity compared to adults, but also to their longevity. Biologic drugs present remarkable advantages in terms of disease control for children, especially in those whose disease cannot be controlled with conventional therapies, but their long-term risks are still being assessed. Data regarding biologic use in children is limited and mostly amounts to case series, but results have been promising, both in terms of controlling disease activity and improving growth parameters. Adverse reactions are infrequent in the short term, but loss of response is a long-term problem, particularly in children. More information is needed about very long term risks. Infliximab and adalimumab are the most studied agents in children, while there is relatively limited data on certolizumab and natalizumab. Further collection of data on these agents is still needed, but this should not restrict access to these agents for children in whom no other agent is effective.