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Grant: Project Grant

Centre hospitalier de l'Université de Montréal (CHUM)

$718,631.00

Interfering with HIV persistence in CD4+ T cells during antiretroviral therapy

FY 2015-16

Summary
HIV/AIDS continues to impact the health of millions of people worldwide. Advances in the treatment of HIV infection have dramatically reduced the death rate from AIDS and improved the quality of life of many HIV-infected patients. Despite this unquestioned success, effective therapy does not eradicate HIV and requires life-long adherence. In addition, the possible long-term toxicity associated with antiretroviral therapy (ART), resistance, stigma and cost all contribute to the necessity of finding a cure. In infected individuals taking ART, HIV persists in a small number of cells that can survive for the lifetime of the infected host. This pool of persistently infected cells, usually referred as the "reservoir for HIV infection", is the main barrier to HIV eradication. The overarching goal of this project is to develop therapeutic strategies aimed at reducing the size of the reservoir, with the ultimate objective of finding a cure for HIV infection. Multiple gaps still exist in our understanding of the basic mechanisms involved in the maintenance of the HIV reservoir. We propose to identify the cells in which HIV persists in the blood and tissues (such as the gut) of HIV-infected individuals taking ART. We will isolate the cells carrying HIV from these anatomical reservoirs. This will allow us to characterize the mechanisms by which HIV is able to persist in these cells. We will then test the ability of several drugs at interfering with HIV persistence in these cells and identify combinations that will lead to the death of the reservoir cells. Our goal is to identify a combination of drugs that can eliminate all latently infected cells in HIV-infected individuals. The results from these studies will constitute the basis for the design of a clinical trial aimed at eradicating HIV.
Program
Project Grant
Location
Quebec, Canada
Recipient Type
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
344281
Name
Chomont Nicolas
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Interfering with HIV persistence in CD4+ T cells during antiretroviral therapy
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$718,631
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Antiretroviral Therapy; Hiv Cure; Hiv Eradication; Hiv Latency; Hiv Reservoir; Hiv Transcription; Latency Reversing Agent; Lymph Node; Memory Cd4+ T Cells; Shock And Kill
Abstract
HIV/AIDS continues to impact the health of millions of people worldwide. Advances in the treatment of HIV infection have dramatically reduced the death rate from AIDS and improved the quality of life of many HIV-infected patients. Despite this unquestioned success, effective therapy does not eradicate HIV and requires life-long adherence. In addition, the possible long-term toxicity associated with antiretroviral therapy (ART), resistance, stigma and cost all contribute to the necessity of finding a cure. In infected individuals taking ART, HIV persists in a small number of cells that can survive for the lifetime of the infected host. This pool of persistently infected cells, usually referred as the "reservoir for HIV infection", is the main barrier to HIV eradication. The overarching goal of this project is to develop therapeutic strategies aimed at reducing the size of the reservoir, with the ultimate objective of finding a cure for HIV infection. Multiple gaps still exist in our understanding of the basic mechanisms involved in the maintenance of the HIV reservoir. We propose to identify the cells in which HIV persists in the blood and tissues (such as the gut) of HIV-infected individuals taking ART. We will isolate the cells carrying HIV from these anatomical reservoirs. This will allow us to characterize the mechanisms by which HIV is able to persist in these cells. We will then test the ability of several drugs at interfering with HIV persistence in these cells and identify combinations that will lead to the death of the reservoir cells. Our goal is to identify a combination of drugs that can eliminate all latently infected cells in HIV-infected individuals. The results from these studies will constitute the basis for the design of a clinical trial aimed at eradicating HIV.
Competitiondate
201603
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Chomont, Nicolas
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $718,631~ $0~