Grant: Project Grant
University of British Columbia
$573,375.00
Modifying colonic inflammation and disease with novel helminth-derived small molecules
FY 2015-16
Summary
Inflammatory bowel diseases (IBD) like Crohn's disease and Ulcerative Colitis affect nearly 250,000 Canadians, and more than 10,000 new cases are diagnosed every year. IBD is characterized by periods of extreme gastrointestinal dysfunction, which significantly impacts patient quality-of-life. IBD patient care involves multiple drugs and may require invasive surgeries if drug intervention is unsuccessful. Collectively, the impact on Canada's economy, in work force and health care costs exceeds $2.8 billion annually. Although the exact cause of IBD is unknown, current treatment strategies aim to suppress the inappropriate and hyperactive intestinal immune responses. However, these immunoregulatory treatments can increase susceptibility to viral infection, a side effect that further diminishes patient quality of life and contributes to IBD-related hospital admissions. New treatment strategies are necessary, and ideally would result in successful control of disease symptoms without increasing the risk of infection.
The goal of this research is to test the efficacy of newly discovered family of compounds (called ascarosides) to limit IBD-like symptoms. Ascarosides are natural by-products of intestinal worms. Notably, intestinal worms can prevent IBD in mice and are currently being tested as a new IBD treatment for humans. Our new preliminary data suggests that ascarosides can ameliorate IBD symptoms by altering the disease-associated hyperactive immune response in the intestines but do not impair the ability to clear viral infection. Using ascarosides could by-pass the need to utilize live worms as therapy, which is both unappealing to patients and has unknown side effects.
Ascarosides have the potential to be highly efficacious and cost-effective small molecule drugs, with minimal adverse effects. Investing in Canadian research that aims to pioneer the pre-clinical drug testing for this product has the potential to considerably improve IBD patient quality of life.
Department
Program
Project Grant
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
346726
Name
Osborne Lisa
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Modifying colonic inflammation and disease with novel helminth-derived small molecules
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$573,375
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Commensal-Specific T Cells; Immunomodulation; Innate And Adaptive Immunity; Mucosal Immunology; Resolution Of Inflammation; Small-Molecule Therapeutics
Abstract
Inflammatory bowel diseases (IBD) like Crohn's disease and Ulcerative Colitis affect nearly 250,000 Canadians, and more than 10,000 new cases are diagnosed every year. IBD is characterized by periods of extreme gastrointestinal dysfunction, which significantly impacts patient quality-of-life. IBD patient care involves multiple drugs and may require invasive surgeries if drug intervention is unsuccessful. Collectively, the impact on Canada's economy, in work force and health care costs exceeds $2.8 billion annually. Although the exact cause of IBD is unknown, current treatment strategies aim to suppress the inappropriate and hyperactive intestinal immune responses. However, these immunoregulatory treatments can increase susceptibility to viral infection, a side effect that further diminishes patient quality of life and contributes to IBD-related hospital admissions. New treatment strategies are necessary, and ideally would result in successful control of disease symptoms without increasing the risk of infection.
The goal of this research is to test the efficacy of newly discovered family of compounds (called ascarosides) to limit IBD-like symptoms. Ascarosides are natural by-products of intestinal worms. Notably, intestinal worms can prevent IBD in mice and are currently being tested as a new IBD treatment for humans. Our new preliminary data suggests that ascarosides can ameliorate IBD symptoms by altering the disease-associated hyperactive immune response in the intestines but do not impair the ability to clear viral infection. Using ascarosides could by-pass the need to utilize live worms as therapy, which is both unappealing to patients and has unknown side effects.
Ascarosides have the potential to be highly efficacious and cost-effective small molecule drugs, with minimal adverse effects. Investing in Canadian research that aims to pioneer the pre-clinical drug testing for this product has the potential to considerably improve IBD patient quality of life.
Competitiondate
201603
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Osborne, Lisa
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $573,375~ $0~