Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
University of British Columbia
$105,000.00
Manipulating immune regulation to improve the success of hematopoietic stem cell transplantation.
EF 2015-16
Résumé
For many blood cancer patients, hematopoietic stem cell transplantation (HSCT, also known as bone marrow transplantation) is the only option for a cure. HSCT works by replacing the patient's blood stem cells with new blood stem cells from a donor. The donated blood stem cells give rise to a new immune system, which can attack and kill the cancer cells in the patient. An unfortunate side effect occurs in up to 80% of HSCT patients when the new immune system attacks the patient's body, leading to a condition called graft-versus-host disease (GVHD). GVHD is a very serious complication that leads to death in about 1/3 of people who develop this side effect.
My research aims to develop new ways to reduce the development of GVHD. I am studying how the powers of a type of immune cell, called a T regulatory cell (or Treg), which naturally prevents unwanted immune responses, can be harnessed for treatment of GVHD. In my first aim, I will study how a drug called anti-thymocyte globulin (ATG), which is used in HSCT, affects the development of Tregs. I will also test if there is an association between lower incidence of GVHD and more Tregs. This work will lead to a better understanding of how ATG can lower GVHD and also to new ways to monitor the presence of Tregs in HSCT. In my second aim I will develop a new way to modify Tregs so they can be used like a drug to prevent or treat GVHD. Specifically I will genetically engineer Tregs so their ability to suppress undesired immune responses is tailored for use in HSCT. This work will lay the foundation for a future clinical trial of genetically modified Tregs in HSCT and has applications for thousands of Canadians living with GVHD today.
Programme
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
348003
Name
Dawson Nicholas
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Manipulating immune regulation to improve the success of hematopoietic stem cell transplantation.
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Cellular Therapy; Chimeric Antigen Receptor; Graft-Versus-Host Disease; Hematopoietic Stem Cell Transplant; Hy Antigen; Immune Reconstitution; Immunology; Immunotherapy; Mass Cytometry; Regulatory T Cell
Abstract
For many blood cancer patients, hematopoietic stem cell transplantation (HSCT, also known as bone marrow transplantation) is the only option for a cure. HSCT works by replacing the patient's blood stem cells with new blood stem cells from a donor. The donated blood stem cells give rise to a new immune system, which can attack and kill the cancer cells in the patient. An unfortunate side effect occurs in up to 80% of HSCT patients when the new immune system attacks the patient's body, leading to a condition called graft-versus-host disease (GVHD). GVHD is a very serious complication that leads to death in about 1/3 of people who develop this side effect.
My research aims to develop new ways to reduce the development of GVHD. I am studying how the powers of a type of immune cell, called a T regulatory cell (or Treg), which naturally prevents unwanted immune responses, can be harnessed for treatment of GVHD. In my first aim, I will study how a drug called anti-thymocyte globulin (ATG), which is used in HSCT, affects the development of Tregs. I will also test if there is an association between lower incidence of GVHD and more Tregs. This work will lead to a better understanding of how ATG can lower GVHD and also to new ways to monitor the presence of Tregs in HSCT. In my second aim I will develop a new way to modify Tregs so they can be used like a drug to prevent or treat GVHD. Specifically I will genetically engineer Tregs so their ability to suppress undesired immune responses is tailored for use in HSCT. This work will lay the foundation for a future clinical trial of genetically modified Tregs in HSCT and has applications for thousands of Canadians living with GVHD today.
Competitiondate
201510
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Dawson, Nicholas
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~