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Grant: Team Grant: Human Immunology Initiative: Research Teams - CIHR-JDRF Pool

University of British Columbia

$800,000.00

Innate and adaptive immune regulation in human type 1 diabetes

FY 2019-20

Summary
Type 1 diabetes (T1D) is an autoimmune disease caused by the immune system mistakenly killing the cells in the pancreas that produce the hormone, insulin. Without insulin, the body cannot regulate blood sugar and this can be life threatening. Insulin can be taken by injection (by syringe or insulin pump), but this cannot replace the natural ability of the pancreas to make insulin only when it is needed, and at the exact level needed. Hence, people with T1D face a lifetime of fluctuating blood sugar and run the risk of life-threatening highs and lows. A true cure for T1D requires the immune system to be re-set so it no longer attacks the pancreas, combined with regeneration of the insulin-producing cells. In this project we aim to assemble a unique cross-Canada team of experts in immune cell biology and diabetes, in order to study specific aspects of how the immune system kills insulin-producing cells (called beta cells) to cause T1D. First, we will collect blood samples from individuals with T1D, another autoimmune disease, or healthy controls. We will then use these blood samples to study how different aspects of the immune system change over time in T1D vs non-T1D subjects, to learn how immune changes correlate with beta cell changes. Results will also be analyzed to determine whether any observed changes are different in males versus females. Second, we will study how three promising types of immune cell therapies might be applied in T1D. We will study how these immune cell therapies might affect beta cell function/regeneration and develop new ways to apply such therapies as a treatment for T1D. Overall, this research will explore several never-before-investigated aspects of T1D biology and take existing therapeutic concepts a step closer to use in the clinic. We will also create synergy with other on-going international studies in T1D and further strengthen our research capacity in this domain.
Program
Team Grant: Human Immunology Initiative: Research Teams - CIHR-JDRF Pool
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
411421
Name
Levings Megan K
Region
British Columbia
Country
Canada
Orgtype
Research Institution; Institution Paid
Partnername
Breakthrough T1D Canada (Ontario)
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
Team Grant : Human Immunology Initiative: Research Teams
Projecttitle
Innate and adaptive immune regulation in human type 1 diabetes
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$800,000
Cihrequipment2
$0
Programname2
Team Grant: Human Immunology Initiative: Research Teams - CIHR-JDRF Pool
Keyworddelim
Biomarkers; Cell Therapy; Immune Regulation; Tissue Immunity; Type 1 Diabetes
Abstract
Type 1 diabetes (T1D) is an autoimmune disease caused by the immune system mistakenly killing the cells in the pancreas that produce the hormone, insulin. Without insulin, the body cannot regulate blood sugar and this can be life threatening. Insulin can be taken by injection (by syringe or insulin pump), but this cannot replace the natural ability of the pancreas to make insulin only when it is needed, and at the exact level needed. Hence, people with T1D face a lifetime of fluctuating blood sugar and run the risk of life-threatening highs and lows. A true cure for T1D requires the immune system to be re-set so it no longer attacks the pancreas, combined with regeneration of the insulin-producing cells. In this project we aim to assemble a unique cross-Canada team of experts in immune cell biology and diabetes, in order to study specific aspects of how the immune system kills insulin-producing cells (called beta cells) to cause T1D. First, we will collect blood samples from individuals with T1D, another autoimmune disease, or healthy controls. We will then use these blood samples to study how different aspects of the immune system change over time in T1D vs non-T1D subjects, to learn how immune changes correlate with beta cell changes. Results will also be analyzed to determine whether any observed changes are different in males versus females. Second, we will study how three promising types of immune cell therapies might be applied in T1D. We will study how these immune cell therapies might affect beta cell function/regeneration and develop new ways to apply such therapies as a treatment for T1D. Overall, this research will explore several never-before-investigated aspects of T1D biology and take existing therapeutic concepts a step closer to use in the clinic. We will also create synergy with other on-going international studies in T1D and further strengthen our research capacity in this domain.
Competitiondate
201906
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Levings, Megan K
Approvedterm
4 ans 0 mois
Cihrcontribution2
Inst of Infection & Immunity~ $800,000~ $0~