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Grant: Project Grant

University of Toronto

$673,200.00

The metabolic basis of T cell exhaustion in HIV infection: discovery of novel treatment targets

EF 2016-17

Résumé
75,500 Canadians were living with Human Immunodeficiency Virus type 1 (HIV) infection in 2014 ,incidence rates are not clearly declining, and about 20% are unaware of infection. Combination antiretroviral therapy to prevent AIDS is lifelong costing over $800,000.00 /person. The reason why HIV needs to be treated lifelong is due to persistence of the virus in persons as a 'virus reservoir'. Interventions targeting viral reservoirs that would shorten or eliminate cART duration would result in substantial cost savings to society and less morbidity from persistent HIV infection. There is also no vaccine on the horizon. The current research program aims to study the immune system of humans against HIV in order to better 'educate' the immune system to eliminate the persistent virus reservoir and to improve the current ineffective vaccines. Our previous work has looked at how a crucial immune cell, the cytotoxic killer CD8 T cell is unable to eliminate HIV from the body. We previously showed that these cells are defective in their killing ability. Recent insights have shown that metabolism of these cells could be abnormal, causing the virus to escape from them. The current project will identify what metabolic defects are present in these cells so that they can be altered by drug treatment or immune therapies, to allow the killer cells to eliminate the virus from the body or prevent virus taking hold with a vaccine.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
354423
Name
Ostrowski Mario A
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
The metabolic basis of T cell exhaustion in HIV infection: discovery of novel treatment targets
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$673,200
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Aids; Ctl; Hiv; Hiv Cure; Immune Control Of Virus; Immunotherapy; Metabolism; T Cell Exhaustion; T Cell Killing
Abstract
75,500 Canadians were living with Human Immunodeficiency Virus type 1 (HIV) infection in 2014 ,incidence rates are not clearly declining, and about 20% are unaware of infection. Combination antiretroviral therapy to prevent AIDS is lifelong costing over $800,000.00 /person. The reason why HIV needs to be treated lifelong is due to persistence of the virus in persons as a 'virus reservoir'. Interventions targeting viral reservoirs that would shorten or eliminate cART duration would result in substantial cost savings to society and less morbidity from persistent HIV infection. There is also no vaccine on the horizon. The current research program aims to study the immune system of humans against HIV in order to better 'educate' the immune system to eliminate the persistent virus reservoir and to improve the current ineffective vaccines. Our previous work has looked at how a crucial immune cell, the cytotoxic killer CD8 T cell is unable to eliminate HIV from the body. We previously showed that these cells are defective in their killing ability. Recent insights have shown that metabolism of these cells could be abnormal, causing the virus to escape from them. The current project will identify what metabolic defects are present in these cells so that they can be altered by drug treatment or immune therapies, to allow the killer cells to eliminate the virus from the body or prevent virus taking hold with a vaccine.
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Ostrowski, Mario A
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $673,200~ $0~