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Grant: Operating Grant - PA: CHVI Vaccine Discovery and Social Research

Centre hospitalier de l'Université de Montréal (CHUM)

$320,616.00

Conformational changes of HIV-1 envelope induced by CD4: a new mechanism governing sensitivity to ADCC

FY 2013-14

Summary
In the absence of treatment, human immunodeficiency virus (HIV) causes acquired immunodeficiency syndrome (AIDS), which has already killed more than 34 million people worldwide. To be able to spread, HIV needs first to enter human cells. To do so, HIV has developed a unique key (envelope glycoproteins, gp120 and gp41) that recognizes a particular lock (receptor CD4 and coreceptors CCR5 or CXCR4) in human cells (mainly lymphocytes T CD4 and macrophages). This key needs to move into the lock (conformational changes of gp120 and gp41) to allow viral entry. In the absence of no effective vaccines against HIV and with therapies aimed at HIV eradication remaining a far fetched goal, new ways to fight HIV infection are warranted. Our preliminary results indicate that antibodies recognizing this key in presence of the receptor CD4 are able to recruit cells from the immune system to eliminate HIV-1-infected cells through a mechanism known as Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC). However, little is known about how this happens and how the virus tries to evade from this response. This proposal will advance our understanding of what could be a critical mechanism required for elimination of HIV-1-infected cells and has the potential to develop new inhibitors or immunogens against the key of HIV.
Program
Operating Grant - PA: CHVI Vaccine Discovery and Social Research
Location
Quebec, Canada
Recipient Type
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
297325
Name
Finzi Andrés
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Virology & Viral Pathogenesis
Projecttitle
Conformational changes of HIV-1 envelope induced by CD4: a new mechanism governing sensitivity to ADCC
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$320,616
Cihrequipment2
$0
Programname2
Operating Grant - PA: CHVI Vaccine Discovery and Social Research
Keyworddelim
A32; Adcc; Adcc-Mediating Antibodies; Cd4 Receptor; Envelope Glycoproteins; Hiv-1; Nef; Rv144 Trial; Vpu
Abstract
In the absence of treatment, human immunodeficiency virus (HIV) causes acquired immunodeficiency syndrome (AIDS), which has already killed more than 34 million people worldwide. To be able to spread, HIV needs first to enter human cells. To do so, HIV has developed a unique key (envelope glycoproteins, gp120 and gp41) that recognizes a particular lock (receptor CD4 and coreceptors CCR5 or CXCR4) in human cells (mainly lymphocytes T CD4 and macrophages). This key needs to move into the lock (conformational changes of gp120 and gp41) to allow viral entry. In the absence of no effective vaccines against HIV and with therapies aimed at HIV eradication remaining a far fetched goal, new ways to fight HIV infection are warranted. Our preliminary results indicate that antibodies recognizing this key in presence of the receptor CD4 are able to recruit cells from the immune system to eliminate HIV-1-infected cells through a mechanism known as Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC). However, little is known about how this happens and how the virus tries to evade from this response. This proposal will advance our understanding of what could be a critical mechanism required for elimination of HIV-1-infected cells and has the potential to develop new inhibitors or immunogens against the key of HIV.
Competitiondate
201309
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Finzi, Andrés
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $320,616~ $0~