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Grant: Project Grant

University of Ottawa

$745,875.00

IL-18: A KEY CYTOKINE LINKING METABOLISM TO IMMUNITY IN NATURAL KILLER AND CD8 T CELLS

EF 2017-18

Résumé
Natural killer cells (NK cells) are a type of lymphocyte (white blood cell) and a component of our innate immune system; and serve as a principal cytotoxic cells on early stages of infection. Upon infection, the inflammatory signals induce a metabolic change in immune cells as they shift from a quiescent status to an activated status, resulting in increased proliferation, and effector molecule production. We reasoned that metabolic demands for intense NK cell proliferation during infection can be fulfilled by high expression of nutrient transporters by cytokines (small soluble mediators). The current project is focused on crosstalk among enhanced nutrient demand, modulation of nutrient transporters, and their regulation by cytokines during infections. NK cells are at the forefront of immunology, and the results of this investigation will help us to modulate immune reactions, thereby providing new insights for therapeutic intervention during infection and inflammation.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
370368
Name
Lee Seung-Hwan
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Immunology & Transplantation
Projecttitle
IL-18: A KEY CYTOKINE LINKING METABOLISM TO IMMUNITY IN NATURAL KILLER AND CD8 T CELLS
Programtype2
Operating Grants
Orgnameinp2
University of Ottawa
Cihramount2
$745,875
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cytokines; Essential Amino Acids; Il-18; Immunometabolism; Mtorc1; Natural Killer Cells; Nutrient Transporters; Virus Infection
Abstract
Natural killer cells (NK cells) are a type of lymphocyte (white blood cell) and a component of our innate immune system; and serve as a principal cytotoxic cells on early stages of infection. Upon infection, the inflammatory signals induce a metabolic change in immune cells as they shift from a quiescent status to an activated status, resulting in increased proliferation, and effector molecule production. We reasoned that metabolic demands for intense NK cell proliferation during infection can be fulfilled by high expression of nutrient transporters by cytokines (small soluble mediators). The current project is focused on crosstalk among enhanced nutrient demand, modulation of nutrient transporters, and their regulation by cytokines during infections. NK cells are at the forefront of immunology, and the results of this investigation will help us to modulate immune reactions, thereby providing new insights for therapeutic intervention during infection and inflammation.
Competitiondate
201709
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Lee, Seung-Hwan
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $745,875~ $0~