Grant: Project Grant
University of Alberta
$895,050.00
Ontogeny of T cell control by BTLA and PD-1
EF 2021-22
Résumé
It is being increasingly found that factors that occur very early in life can promote the generation of disease later in life, and this is also true for autoimmune diseases. Our research focuses on two molecules, receptors known as PD-1 and BTLA, present on the surface of some immune system cells. Strong evidence supports the concept that these receptors are involved in preventing our immune system attacking our own cells/tissues. We will examine genetically engineered animals that will lack the function of these receptors at different stages in the life of the animal and in the life of the immune cells. We hypothesize that these receptors are particularly important early in life on newly generated immune cells and that their early action is necessary to prevent later life susceptibility to autoimmune disease. Identifying when and where these receptors are needed will be critical to the future design of medicines that prevent or stop autoimmune disease.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
461624
Name
Anderson Colin C
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Immunology & Transplantation
Projecttitle
Ontogeny of T cell control by BTLA and PD-1
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$895,050
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Autoimmune Disease; Immunologic Tolerance
Abstract
It is being increasingly found that factors that occur very early in life can promote the generation of disease later in life, and this is also true for autoimmune diseases. Our research focuses on two molecules, receptors known as PD-1 and BTLA, present on the surface of some immune system cells. Strong evidence supports the concept that these receptors are involved in preventing our immune system attacking our own cells/tissues. We will examine genetically engineered animals that will lack the function of these receptors at different stages in the life of the animal and in the life of the immune cells. We hypothesize that these receptors are particularly important early in life on newly generated immune cells and that their early action is necessary to prevent later life susceptibility to autoimmune disease. Identifying when and where these receptors are needed will be critical to the future design of medicines that prevent or stop autoimmune disease.
Competitiondate
202203
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Anderson, Colin C; Baldwin, Troy A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $895,050~ $0~