Grant: Collaborative Health Research Projects
University of British Columbia
$206,608.00
Bioprocess Engineering for Therapeutic T-cell Manufacturing
EF 2020-21
Résumé
Emerging cultured cell therapies have the potential to treat or cure multiple degenerative and fatal diseases, and hundreds of cell immunotherapy clinical trials are currently underway. The first two immune cell (T-cell) therapies approved in 2017 are highly effective, and can treat blood-cell cancers for which no treatment options remained. In contrast to using
chemotherapy to kill cancer cells, these T-cell immunotherapies are based on amplifying natural human defences to kill cancer cells. This proposal is focussed on producing T cells that suppress other immune cells going after the wrong target, such as in transplant rejection or autoimmune disorders. These cell therapies could replace the use of immunosuppressive
drugs that are often ineffective and have many negative side effects. Although cell immunotherapy is poised to revolutionize medical treatments, many challenges must be overcome to make these therapies a reality for the many patients needing them. As the culture of T cells coming from human donors is very complex, we must increase our understanding and control of the processes used to produce these therapeutic cells. This is the focus of our project. We will improve the production of therapeutic cells so that hundreds of patients can be treated with each cell donor. We also seek to enable networked Canadian skills and resources to facilitate clinical trials. Through reducing the cell production costs and increasing the number of cells produced for treatment, we will contribute toward reducing overall costs, to make these treatments economically feasible for our healthcare system and widely available to save lives. Our development of T-cell manufacturing technology will be systematically networked with Canadian cell therapy manufacturing facilities to broadly inform this and other promising clinical treatments that depend on cell manufacturing.
Programme
Collaborative Health Research Projects
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
538854-2019
Name nom
Piret, James
Department département
Michael Smith Laboratories
Organization id
2
Institution établissement
University of British Columbia
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2020
Competition year année de concours
2019
Award amount
206608
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
9999
Area of application group en
Not available
Area of application group fr
Non disponible
Area of application en
Not available
Area of application fr
Non disponible
Research subject code
1802
Research subject group en
Chemical engineering
Research subject group fr
Génie chimique
Research subject en
Biochemical engineering
Research subject fr
Génie biochimique
Installment
inst:2 - 4
Partie
3
Nb partie
4
Application title
Bioprocess Engineering for Therapeutic T-cell Manufacturing
Keyword
NSERC
Application summary
Emerging cultured cell therapies have the potential to treat or cure multiple degenerative and fatal diseases, and hundreds of cell immunotherapy clinical trials are currently underway. The first two immune cell (T-cell) therapies approved in 2017 are highly effective, and can treat blood-cell cancers for which no treatment options remained. In contrast to using
chemotherapy to kill cancer cells, these T-cell immunotherapies are based on amplifying natural human defences to kill cancer cells. This proposal is focussed on producing T cells that suppress other immune cells going after the wrong target, such as in transplant rejection or autoimmune disorders. These cell therapies could replace the use of immunosuppressive
drugs that are often ineffective and have many negative side effects. Although cell immunotherapy is poised to revolutionize medical treatments, many challenges must be overcome to make these therapies a reality for the many patients needing them. As the culture of T cells coming from human donors is very complex, we must increase our understanding and control of the processes used to produce these therapeutic cells. This is the focus of our project. We will improve the production of therapeutic cells so that hundreds of patients can be treated with each cell donor. We also seek to enable networked Canadian skills and resources to facilitate clinical trials. Through reducing the cell production costs and increasing the number of cells produced for treatment, we will contribute toward reducing overall costs, to make these treatments economically feasible for our healthcare system and widely available to save lives. Our development of T-cell manufacturing technology will be systematically networked with Canadian cell therapy manufacturing facilities to broadly inform this and other promising clinical treatments that depend on cell manufacturing.