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'Off-the-shelf' allogeneic CAR T cells: development and challenges.
S Depil1, P Duchateau2, S A Grupp3
1Centre Léon Bérard and Centre de Recherche en Cancérologie de Lyon, Lyon, France. stephane.depil@lyon.unicancer.fr.
Nature Reviews. Drug Discovery
|January 5, 2020
Summary
Allogeneic chimeric antigen receptor (CAR) T cells offer advantages like immediate availability and lower costs for cancer therapy. Gene editing is being used to create next-generation CAR T cells that minimize graft-versus-host disease risks.
Area of Science:
- Immunology
- Oncology
- Biotechnology
Background:
- Autologous chimeric antigen receptor (CAR) T cell therapy has transformed blood cancer treatment.
- Allogeneic CAR T cells present potential benefits including immediate availability, product standardization, and cost reduction through industrial processes.
Purpose of the Study:
- To review T cell sources for optimal allogeneic CAR T cell therapy.
- To describe technological approaches, primarily gene editing, for producing allogeneic CAR T cells with reduced graft-versus-host disease (GvHD) potential.
Main Methods:
- Review of current literature on T cell sources for allogeneic CAR T cell therapy.
- Analysis of gene editing technologies for modifying allogeneic CAR T cells to mitigate GvHD.
Main Results:
- Allogeneic CAR T cells face challenges including potential GvHD and rapid host immune elimination.
- Next-generation allogeneic CAR T cells are being developed to overcome these limitations.
Conclusions:
- Improved allogeneic CAR T cell products hold promise for advancing cancer treatment.
- Gene editing technologies are crucial for developing safer and more effective allogeneic CAR T cell therapies.
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