Grant: Travel Awards - Institute Community Support
University of Manitoba
$2,700.00
Antigen stimulation drives clonal expansion of latent CD4+ T cells under antiretroviral therapy suppression
FY 2024-25
Summary
Antiretroviral therapy (ART) prevents viral replication in people living with HIV (PLWH), however it does not provide a cure since the virus is not eliminated from the body. As a result, PLWH must remain on ART lifelong and interventions to reduce the size of this reservoir have had limited success, highlighting the need for alternate cure strategies for PLWH. HIV can persist long-term by infecting a reservoir of memory T cells that are naturally adept at long-term survival. HIV targets these memory T cells for infection and exploits their survival abilities. Thus, this project aims to investigate how the virus co-opts the mechanisms utilized by memory cells for its own long-term persistence. T cell receptors are like sensors on the surface of T cells that help them recognize and respond to specific signals from other cells in our body. When the T cell receptor of an infected cell interacts with certain signals, it enhances the growth and survival of the HIV reservoir. By studying how HIV hijacks these interactions to promote its own long-term survival, we hope to uncover strategies to reverse these processes.
Department
Program
Travel Awards - Institute Community Support
Recipient
Location
Manitoba, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
521160
Name
Greenslade Riley
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Travel Awards - Institute Community Support
Projecttitle
Antigen stimulation drives clonal expansion of latent CD4+ T cells under antiretroviral therapy suppression
Programtype2
Undefined
Orgnameinp2
University of Manitoba
Cihramount2
$2,700
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Antigen Driven Clonal Expansion; Hiv Reservoir; Hiv-1; Latency; T Cell Receptor
Abstract
Antiretroviral therapy (ART) prevents viral replication in people living with HIV (PLWH), however it does not provide a cure since the virus is not eliminated from the body. As a result, PLWH must remain on ART lifelong and interventions to reduce the size of this reservoir have had limited success, highlighting the need for alternate cure strategies for PLWH. HIV can persist long-term by infecting a reservoir of memory T cells that are naturally adept at long-term survival. HIV targets these memory T cells for infection and exploits their survival abilities. Thus, this project aims to investigate how the virus co-opts the mechanisms utilized by memory cells for its own long-term persistence. T cell receptors are like sensors on the surface of T cells that help them recognize and respond to specific signals from other cells in our body. When the T cell receptor of an infected cell interacts with certain signals, it enhances the growth and survival of the HIV reservoir. By studying how HIV hijacks these interactions to promote its own long-term survival, we hope to uncover strategies to reverse these processes.
Competitiondate
202501
Approvedterm2
1 yr 0 mth
Pinamesdelim
Greenslade, Riley
Approvedterm
1 an 0 mois
Cihrcontribution2
MI #3~ $2,700~ $0~