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Grant: Project Grant

University of Calgary

$822,376.00

Mechanisms underlying oncolytic rhabdovirus-mediated anticancer immunity

EF 2018-19

Résumé
Oncolytic viruses (OVs) are being used to treat cancer patients, yet there are major gaps in our understanding of how they work. Although developed to kill cancer cells directly, an increasing body of evidence suggests that their most important function is to engage the body's immune system to attack the cancer. How this happens is complex and not well understood. Preliminary data suggest that oncolytic rhabdoviruses (ORVs) engage anticancer T cell responses by infecting both cancer and normal cells. Our objective is to determine how cancer and non-cancer cell infections contribute to the T cell immune response incited by ORV therapy. This knowledge will inform our and other's efforts to develop more effective ORV-based strategies for treating cancer.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
402835
Name
Mahoney Douglas J
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Biology & Therapeutics
Projecttitle
Mechanisms underlying oncolytic rhabdovirus-mediated anticancer immunity
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$822,376
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cancer; Immunotherapy; Intravital Microscopy; Oncolytic Viruses; Rhabdovirus
Abstract
Oncolytic viruses (OVs) are being used to treat cancer patients, yet there are major gaps in our understanding of how they work. Although developed to kill cancer cells directly, an increasing body of evidence suggests that their most important function is to engage the body's immune system to attack the cancer. How this happens is complex and not well understood. Preliminary data suggest that oncolytic rhabdoviruses (ORVs) engage anticancer T cell responses by infecting both cancer and normal cells. Our objective is to determine how cancer and non-cancer cell infections contribute to the T cell immune response incited by ORV therapy. This knowledge will inform our and other's efforts to develop more effective ORV-based strategies for treating cancer.
Competitiondate
201903
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Mahoney, Douglas J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $822,376~ $0~