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Grant: Doctoral Research Award: Canada Graduate Scholarships

University of British Columbia

$105,000.00

Development of MHC Class II-targeted chimeric antigen receptor regulatory T cell (Treg) therapies for solid organ transplantation

EF 2023-24

Résumé
Organ transplantation is a life-saving procedure for people with severe organ failure. Since the immune system sees the new organ as foreign and attempts to destroy it, transplant recipients must take immunosuppressive drugs for the rest of their lives to prevent rejection. Unfortunately, these drugs also prevent the immune system from carrying out its normal functions, which places transplant recipients at high risk of infection and cancer. Regulatory T cells (Tregs) are a specialized type of immune cell that specifically suppress overactive immune responses. As such, using Tregs as a cell therapy, by infusing the cells into a transplant recipient's bloodstream, is a promising approach to preventing transplant rejection. Treg therapy is safe, with few side effects, but there are several challenges to address. For example, Tregs do not survive and persist long-term after infusion, and become 'exhausted' with constant overstimulation, causing them to lose immune-suppressive function over time. To address this, my work aims to improve Treg therapy by increasing potency and specificity, and improving how long Tregs persist and remain effective in the body. I will use genetic engineering to alter Tregs so they can specifically target a molecule called MHC II. MHC II is found on certain types of immune cells that contribute to transplant rejection by producing antibodies and activating T cells targeting the new organ. Because MHC II levels in transplanted organs are low at baseline but increase with inflammation, Tregs targeting MHC II could be less likely to become exhausted: instead of receiving constant overstimulation, they would specifically receive stimulation from MHC II when needed, during inflammatory rejection of the transplanted organ. Ultimately, my goal is to improve Treg therapies to eventually replace or reduce the need for immunosuppressive drugs, decreasing mortality and improving quality of life for people who undergo organ transplantation.
Programme
Doctoral Research Award: Canada Graduate Scholarships
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
497286
Name
HALVORSON TORIN J
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Development of MHC Class II-targeted chimeric antigen receptor regulatory T cell (Treg) therapies for solid organ transplantation
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Research Award: Canada Graduate Scholarships
Keyworddelim
Alloimmunity; Chimeric Antigen Receptors; Co-Detection By Indexing; Flow Cytometry; Immune Suppression; Immune Tolerance; Major Histocompatibility Complexes; Regulatory T Cells; Skin Transplant Models; Solid Organ Transplantation
Abstract
Organ transplantation is a life-saving procedure for people with severe organ failure. Since the immune system sees the new organ as foreign and attempts to destroy it, transplant recipients must take immunosuppressive drugs for the rest of their lives to prevent rejection. Unfortunately, these drugs also prevent the immune system from carrying out its normal functions, which places transplant recipients at high risk of infection and cancer. Regulatory T cells (Tregs) are a specialized type of immune cell that specifically suppress overactive immune responses. As such, using Tregs as a cell therapy, by infusing the cells into a transplant recipient's bloodstream, is a promising approach to preventing transplant rejection. Treg therapy is safe, with few side effects, but there are several challenges to address. For example, Tregs do not survive and persist long-term after infusion, and become 'exhausted' with constant overstimulation, causing them to lose immune-suppressive function over time. To address this, my work aims to improve Treg therapy by increasing potency and specificity, and improving how long Tregs persist and remain effective in the body. I will use genetic engineering to alter Tregs so they can specifically target a molecule called MHC II. MHC II is found on certain types of immune cells that contribute to transplant rejection by producing antibodies and activating T cells targeting the new organ. Because MHC II levels in transplanted organs are low at baseline but increase with inflammation, Tregs targeting MHC II could be less likely to become exhausted: instead of receiving constant overstimulation, they would specifically receive stimulation from MHC II when needed, during inflammatory rejection of the transplanted organ. Ultimately, my goal is to improve Treg therapies to eventually replace or reduce the need for immunosuppressive drugs, decreasing mortality and improving quality of life for people who undergo organ transplantation.
Competitiondate
202311
Approvedterm2
3 yrs 0 mth
Pinamesdelim
HALVORSON, TORIN J
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~