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Grant: Project Grant

University of Ottawa

$1,162,800.00

Developing Natural Killer Cell-Mediated Combination Immunotherapies for the Treatment of Multiple Myeloma

EF 2023-24

Résumé
Natural Killer (NK) cells are pivotal in anti-tumor immunity, with promising interest in their engineering to enhance cancer cell eradication capabilities. Chimeric Antigen Receptors (CAR) represent transformative synthetic constructs, integrated into NK cells, that facilitate the specific recognition and killing of cancerous cells. Initial clinical trials have showcased CAR-NK cells as a dynamic 'living drug', capable of triggering robust anti-tumor responses in cancer patients. However, the emergence of evasive cancer cells lacking the targeted CAR antigen poses a significant challenge, undermining the efficacy of NK cell-based therapies. To address this obstacle, we propose a strategy of simultaneous targeting of multiple tumor antigens. This approach aims to circumvent antigen evasion, laying the groundwork for a more effective NK cell therapy.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
500822
Name
Lee Seung-Hwan
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Biology & Therapeutics
Projecttitle
Developing Natural Killer Cell-Mediated Combination Immunotherapies for the Treatment of Multiple Myeloma
Programtype2
Operating Grants
Orgnameinp2
University of Ottawa
Cihramount2
$1,162,800
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Chimeric Activating Receptors; Crispr/Cas9 Genome Editing; Cytokines; Genetic Engineering; Immunotherapy; Multiple Myeloma; Natural Killer Cells
Abstract
Natural Killer (NK) cells are pivotal in anti-tumor immunity, with promising interest in their engineering to enhance cancer cell eradication capabilities. Chimeric Antigen Receptors (CAR) represent transformative synthetic constructs, integrated into NK cells, that facilitate the specific recognition and killing of cancerous cells. Initial clinical trials have showcased CAR-NK cells as a dynamic 'living drug', capable of triggering robust anti-tumor responses in cancer patients. However, the emergence of evasive cancer cells lacking the targeted CAR antigen poses a significant challenge, undermining the efficacy of NK cell-based therapies. To address this obstacle, we propose a strategy of simultaneous targeting of multiple tumor antigens. This approach aims to circumvent antigen evasion, laying the groundwork for a more effective NK cell therapy.
Competitiondate
202403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Lee, Seung-Hwan
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,162,800~ $0~