Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
University of Manitoba
$105,000.00
Human cathelicidin peptide LL-37 and its derivative IG-19 regulate IL-32-induced inflammation and provide protection in a murine model of arthritis
FY 2013-14
Summary
Rheumatoid arthritis and related inflammatory arthritis diseases collectively affect 16% of Canadians with an estimated socio-economic burden of $6 billion annually. The symptoms associated with these debilitating diseases are the result of an underlying state of chronic inflammation. Current treatments for inflammatory arthritis and other chronic inflammatory diseases directly inhibit critical molecules of the immune system. As a result these treatments often have the unwanted side effects of making patients more susceptible to infections and sometimes the development of certain cancers. Therefore, there is an urgent need for new treatment methods that do not produce the negative side effects of the current therapies for controlling chronic inflammatory diseases.
We have shown that a group of small molecules known as host defence peptides can suppress inflammation while maintaining the immune system's ability to control infections. This dual function makes them attractive candidates as potential therapeutics for chronic inflammatory diseases including arthritis. In our recent studies, we have identified specific peptide candidates that can control rheumatoid arthritis in mice. We have now established the experimental tools and animal models that will allow us to more fully examine the activity of these peptides in the context of inflammatory arthritis.
In this project, we will study the biological effects of the host defence peptides during the different stages of disease progression in a mouse model of rheumatoid arthritis. The results from this project will support the development of new peptide therapeutics for inflammatory arthritis, and will also identify new drug targets that can potentially be used to identify future anti-inflammatory therapeutics.
Department
Program
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Recipient
Location
Manitoba, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
307741
Name
Choi Ka-Yee Grace
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Human cathelicidin peptide LL-37 and its derivative IG-19 regulate IL-32-induced inflammation and provide protection in a murine model of arthritis
Programtype2
Studentship Programs
Orgnameinp2
University of Manitoba
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Cathelicidin Ll37; Cytokine Il-32; Host Defense Peptide; Immune Regulation; Inflammation; Inflammatory Arthritis; Mouse Model Of Arthritis; Proteomics; Signal Transduction
Abstract
Rheumatoid arthritis and related inflammatory arthritis diseases collectively affect 16% of Canadians with an estimated socio-economic burden of $6 billion annually. The symptoms associated with these debilitating diseases are the result of an underlying state of chronic inflammation. Current treatments for inflammatory arthritis and other chronic inflammatory diseases directly inhibit critical molecules of the immune system. As a result these treatments often have the unwanted side effects of making patients more susceptible to infections and sometimes the development of certain cancers. Therefore, there is an urgent need for new treatment methods that do not produce the negative side effects of the current therapies for controlling chronic inflammatory diseases.
We have shown that a group of small molecules known as host defence peptides can suppress inflammation while maintaining the immune system's ability to control infections. This dual function makes them attractive candidates as potential therapeutics for chronic inflammatory diseases including arthritis. In our recent studies, we have identified specific peptide candidates that can control rheumatoid arthritis in mice. We have now established the experimental tools and animal models that will allow us to more fully examine the activity of these peptides in the context of inflammatory arthritis.
In this project, we will study the biological effects of the host defence peptides during the different stages of disease progression in a mouse model of rheumatoid arthritis. The results from this project will support the development of new peptide therapeutics for inflammatory arthritis, and will also identify new drug targets that can potentially be used to identify future anti-inflammatory therapeutics.
Competitiondate
201310
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Choi, Ka-Yee Grace
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~