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Grant: CIHR Fellowship

Direct Payment

$150,000.00

A genome editing platform for therapeutic editing of immune cells

EF 2018-19

Résumé
To address the need for therapies that eliminate HIV infection, we propose development of a new method to deliver non-viral genome editing enzymes to the immune cells within the body to render them resistant to the virus. The specialized genome editing enzymes we develop will be targeted specifically to immune cells at the front lines of HIV infection, turning off genes required for HIV infectivity and eliminating the need for continued antiretroviral therapy. This method will be compatible with intravenous administration, preventing the expensive and labor-intensive ex vivo procedures currently associated with immune cell genome editing. Once this technology is developed it will be adaptable to correcting mutations associated with genetic diseases, as we will be able to replace the immune-cell targeting moiety to recognize other cells and tissues and program the genome editing enzymes to edit the gene of interest. The ability to perform genome editing of specific human cells and tissues in vivo will be transformative to the field of therapeutic genome editing, drastically improving access to genetic therapies.
Programme
CIHR Fellowship
Bénéficiaire
Emplacement
California, United States of America
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
397341
Name
Foss Dana V
Region
California
Country
United States of America
Orgtype
Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
A genome editing platform for therapeutic editing of immune cells
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Crispr Genome Editing; Hiv Therapeutics; Non-Viral Delivery Of Cas9 Rnp; Tissue Specific Genome Editing
Abstract
To address the need for therapies that eliminate HIV infection, we propose development of a new method to deliver non-viral genome editing enzymes to the immune cells within the body to render them resistant to the virus. The specialized genome editing enzymes we develop will be targeted specifically to immune cells at the front lines of HIV infection, turning off genes required for HIV infectivity and eliminating the need for continued antiretroviral therapy. This method will be compatible with intravenous administration, preventing the expensive and labor-intensive ex vivo procedures currently associated with immune cell genome editing. Once this technology is developed it will be adaptable to correcting mutations associated with genetic diseases, as we will be able to replace the immune-cell targeting moiety to recognize other cells and tissues and program the genome editing enzymes to edit the gene of interest. The ability to perform genome editing of specific human cells and tissues in vivo will be transformative to the field of therapeutic genome editing, drastically improving access to genetic therapies.
Competitiondate
201811
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Foss, Dana V
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~