Grant: Operating Grant
University of Manitoba
$606,266.00
Defining the mechanisms of IRF1 in mediating innate resistance to mucosal HIV acquisition in HIV exposed seronegative (HESN) women.
FY 2012-13
Summary
The ultimate solution to the HIV/AIDS pandemic, still, one of the greatest health issues facing humankind, is the development of an effective vaccine or microbicide. Almost all vaccines were derived out of an understanding, no matter how primitive, of what results in protective immunity. We seek to understand the mechanisms of natural protection against HIV in women who are highly exposed to HIV yet escape infection. Our earlier genetic studies showed that these HIV resistant women have reduced IRF1 expression in their blood cells. IRF-1 is an important regulator of human immunity and HIV replication. To determine how IRF1 works in in protecting against HIV infection, this study will examine how artificially reducing IRF1 levels in cells and tissue from the female genital tract will limit HIV infection, and/or alter host immune responses at this site. Findings from this study will generate new knowledge to determine if specifically reducing IRF1 will protect against HIV infection and if artificially reducing IRF1 could lead to the eventual development of an effective HIV vaccine, microbicide or novel prevention strategy.
Department
Program
Operating Grant
Recipient
Location
Manitoba, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
280448
Name
Ball Terry B
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Virology & Viral Pathogenesis
Projecttitle
Defining the mechanisms of IRF1 in mediating innate resistance to mucosal HIV acquisition in HIV exposed seronegative (HESN) women.
Programtype2
Operating Grants
Orgnameinp2
University of Manitoba
Cihramount2
$606,266
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Africa; Genetics; Hesn; Hiv; Innate; Irf1; Microbicide; Mucosal; Prevention; Resistance
Abstract
The ultimate solution to the HIV/AIDS pandemic, still, one of the greatest health issues facing humankind, is the development of an effective vaccine or microbicide. Almost all vaccines were derived out of an understanding, no matter how primitive, of what results in protective immunity. We seek to understand the mechanisms of natural protection against HIV in women who are highly exposed to HIV yet escape infection. Our earlier genetic studies showed that these HIV resistant women have reduced IRF1 expression in their blood cells. IRF-1 is an important regulator of human immunity and HIV replication. To determine how IRF1 works in in protecting against HIV infection, this study will examine how artificially reducing IRF1 levels in cells and tissue from the female genital tract will limit HIV infection, and/or alter host immune responses at this site. Findings from this study will generate new knowledge to determine if specifically reducing IRF1 will protect against HIV infection and if artificially reducing IRF1 could lead to the eventual development of an effective HIV vaccine, microbicide or novel prevention strategy.
Competitiondate
201303
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Ball, Terry B
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $606,266~ $0~