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Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships

University of British Columbia

$105,000.00

Defining the biology and therapeutic potential of human T regulatory cells with tissue repair function

EF 2016-17

Résumé
Transplantation can be a life-saving treatment for patients in organ failure. Unfortunately, transplant rejection, when the patient's immune system destroys the new organ, is a major cause of illness and death. Patients must take anti-rejection drugs for the rest of their life, which do not always work and have many side effects. Our goal is to replace these drugs with a safer and more effective therapy that will protect the transplanted organs over the long term. One promising strategy is to infuse patients with a dose of a special type of white blood cell, called T regulatory cells (Tregs). Tregs normally balance (regulate) the immune system by stopping unwanted immune responses. Recently, Tregs in mice were found to have a key role in tissue repair, which was needed to recover from infections and injuries. Tissue-reparative Tregs may exist in humans as well, but little is known about how to promote this function in patients. In this project, we will see whether human Tregs in the blood, skin, fat, and lung fluid can also mediate tissue repair, and what external signals are needed for these cells to work. We will also modify Tregs to boost their tissue repair potential, and test whether they can better protect against organ rejection and damage in mouse models. Ultimately, this work will contribute to the application of tissue-reparative Tregs as cell therapy both for transplant patients and others at risk of immune-mediated tissue damage.
Programme
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
365443
Name
Lam Avery J
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Defining the biology and therapeutic potential of human T regulatory cells with tissue repair function
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
Amphiregulin; Bronchoalveolar Lavage Fluid; Cell Therapy; Graft Rejection; Human Immunology; Human Tissues; Interleukin-33; Regulatory T Cells; Tissue Repair; Transplantation
Abstract
Transplantation can be a life-saving treatment for patients in organ failure. Unfortunately, transplant rejection, when the patient's immune system destroys the new organ, is a major cause of illness and death. Patients must take anti-rejection drugs for the rest of their life, which do not always work and have many side effects. Our goal is to replace these drugs with a safer and more effective therapy that will protect the transplanted organs over the long term. One promising strategy is to infuse patients with a dose of a special type of white blood cell, called T regulatory cells (Tregs). Tregs normally balance (regulate) the immune system by stopping unwanted immune responses. Recently, Tregs in mice were found to have a key role in tissue repair, which was needed to recover from infections and injuries. Tissue-reparative Tregs may exist in humans as well, but little is known about how to promote this function in patients. In this project, we will see whether human Tregs in the blood, skin, fat, and lung fluid can also mediate tissue repair, and what external signals are needed for these cells to work. We will also modify Tregs to boost their tissue repair potential, and test whether they can better protect against organ rejection and damage in mouse models. Ultimately, this work will contribute to the application of tissue-reparative Tregs as cell therapy both for transplant patients and others at risk of immune-mediated tissue damage.
Competitiondate
201610
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Lam, Avery J
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~