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Grant: Operating Grant

University of British Columbia

$555,957.00

The role of FOXP3 and IL-1-family cytokines in regulating CD4+ T cell subsets in healthy humans, and in patients with chronic skin inflammation.

FY 2012-13

Summary
The immune system is designed to recognize the difference between harmful and non-harmful foreign proteins, and to not react against proteins that normally exist in an individual. Unfortunately, when the processes controlling these functions breakdown diseases such as autoimmunity and allergy can result. Although many different types of white blood cells work together to regulate immune responses, one of the major players is the CD4+ T cell. Via their ability to make proteins that send messages between cells, known as cytokines, CD4+ T cells have a central role in directing immunity in health and disease. We are interested in studying how the development and function of different types of CD4+ T cells is controlled since when they can cause much of the tissue destruction and injury in patients with autoimmune diseases. Our past research has revealed possible new pathways of regulation and in this proposal we will conduct research that is aimed at discovering how these new pathways work. The result will be a better understanding of how CD4+ T cells can cause disease and how their inappropriate function can be turned off in patients with chronic inflammatory diseases. .
Program
Operating Grant
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
266063
Name
Levings Megan K
Region
British Columbia
Country
Canada
Orgtype
Research Institution; Institution Paid
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Immunology & Transplantation
Projecttitle
The role of FOXP3 and IL-1-family cytokines in regulating CD4+ T cell subsets in healthy humans, and in patients with chronic skin inflammation.
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$555,957
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Autoimmunity; Fibroblasts; Graft Versus Host Disease; Inflammasome; Interleukin 1; Skin Inflammation; Systemic Sclerosis; T Helper Cells; T Regulatory Cells; Transplantation
Abstract
The immune system is designed to recognize the difference between harmful and non-harmful foreign proteins, and to not react against proteins that normally exist in an individual. Unfortunately, when the processes controlling these functions breakdown diseases such as autoimmunity and allergy can result. Although many different types of white blood cells work together to regulate immune responses, one of the major players is the CD4+ T cell. Via their ability to make proteins that send messages between cells, known as cytokines, CD4+ T cells have a central role in directing immunity in health and disease. We are interested in studying how the development and function of different types of CD4+ T cells is controlled since when they can cause much of the tissue destruction and injury in patients with autoimmune diseases. Our past research has revealed possible new pathways of regulation and in this proposal we will conduct research that is aimed at discovering how these new pathways work. The result will be a better understanding of how CD4+ T cells can cause disease and how their inappropriate function can be turned off in patients with chronic inflammatory diseases. .
Competitiondate
201209
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Levings, Megan K
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $555,957~ $0~
University of British Columbia - $555,957 Grant (2012… | Canada Spends