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Grant: Project Grant

Centre hospitalier de l'Université de Montréal (CHUM)

$696,150.00

Autophagy in the control of RSV replication in human airway epithelial cells

EF 2017-18

Résumé
Infection by Respiratory Syncytial Virus (RSV) is the causative agent of substantial morbidity and mortality in children, elderly but also all-aged adults with a compromised immune system or cardiopulmonary diseases. Despite intensive research, the development of efficient vaccine or treatment failed. The search for novel RSV treatment remains a priority. Particularly, more information is needed to understand how RSV interacts with cellular mechanisms and how it helps its replication or help the host defense. Identification of these virus-host interactions is necessary to identify novel drug targets amongst cellular proteins. Much remains unknown about how RSV interacts with cellular processes. Our research will address knowledge gaps in the understanding of the host-virus interaction influencing RSV infection. Outputs from this research will lead to the identification of novel targets for the development of urgently needed RSV antiviral therapies.
Programme
Project Grant
Emplacement
Quebec, Canada
Type de bénéficiaire
Not-for-profit organization or charity
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
380201
Name
Grandvaux Nathalie
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Virology & Viral Pathogenesis
Projecttitle
Autophagy in the control of RSV replication in human airway epithelial cells
Programtype2
Operating Grants
Orgnameinp2
Centre hospitalier de l'Université de Montréal (CHUM)
Cihramount2
$696,150
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Autophagy; Cellular Signaling; Host-Pathogen Interaction; Secretion; Ubiquitination; Viral Cycle; Virus; Virus Replication; Virus Trafficking
Abstract
Infection by Respiratory Syncytial Virus (RSV) is the causative agent of substantial morbidity and mortality in children, elderly but also all-aged adults with a compromised immune system or cardiopulmonary diseases. Despite intensive research, the development of efficient vaccine or treatment failed. The search for novel RSV treatment remains a priority. Particularly, more information is needed to understand how RSV interacts with cellular mechanisms and how it helps its replication or help the host defense. Identification of these virus-host interactions is necessary to identify novel drug targets amongst cellular proteins. Much remains unknown about how RSV interacts with cellular processes. Our research will address knowledge gaps in the understanding of the host-virus interaction influencing RSV infection. Outputs from this research will lead to the identification of novel targets for the development of urgently needed RSV antiviral therapies.
Competitiondate
201803
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Grandvaux, Nathalie
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $696,150~ $0~