SAMP1/YitFc mouse strain: A spontaneous model of Crohn's disease-like ileitis
- Theresa T. Pizarro(corresponding author),
- Luca Pastorelli,
- Giorgos Bamias,
- Rekha R. Garg,
- Brian K. Reuter,
- Joseph R. Mercado
- Case Western Reserve University,
- IRCCS Policlinico San Donato,
- University of Milan,
- National and Kapodistrian University of Athens,
- University of Alberta,
- National Institute of Gastroenterology
Open access
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
The SAMP1/YitFc mouse strain represents a model of Crohn's disease (CD)-like ileitis that is ideal for investigating the pathogenesis of chronic intestinal inflammation. Different from the vast majority of animal models of colitis, the ileal-specific phenotype characteristic of SAMP1/YitFc mice occurs spontaneously, without genetic, chemical, or immunological manipulation. In addition, SAMP1/YitFc mice possess remarkable similarities to the human condition with regard to disease location, histologic features, incidence of extraintestinal manifestations, and response to conventional therapies. SAMP1/YitFc mice also display a well-defined time course of a predisease state and phases of acute and chronic ileitis. As such, the SAMP1/YitFc model is particularly suitable for elucidating pathways that precede the clinical phenotype that may lead to preventive, and therefore more efficacious, intervention with the natural course of disease, or alternatively, for the development of therapeutic strategies directed against chronic, established ileitis. In this review we summarize important contributions made by our group and others that uncover potential mechanisms in the pathogenesis of CD using this unique murine model of chronic intestinal inflammation.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 2566-2584 (19 pages)Journal (Volume, Issue Number)
Inflammatory Bowel Diseases (Volume 17, Issue 12)Publication milestones
- Published - 12/2011
Publication status
ISSN
1078-0998Publication IDs
- Scopus: 80054861647
- PubMed: 21557393
