Temporal regulation of transgene expression controlled by amino acid availability in human T cells.
Aurore DougéCyrielle VituretValérie CarraroLaurent ParryCécile Coudy-GandilhonRichard LemalLydie CombaretAnne-Catherine MaurinJulien AverousCéline JousseJacques-Olivier BayPierre VerrellePierre FafournouxAlain BruhatPaul-Olivier RouzairePublished in: HLA (2023)
T cell therapy strategies, from allogeneic stem cell transplantation toward genetically-modified T cells infusion, develop powerful anti-tumor effects but are often accompanied by side effects and their efficacy remains sometimes to be improved. It therefore appears important to provide a flexible and easily reversible gene expression regulation system to control T cells activity. We developed a gene expression regulation technology that exploits the physiological GCN2-ATF4 pathway's ability to induce gene expression in T cells in response to one essential amino acid deficiency. We first demonstrated the functionality of NUTRIREG in human T cells by transient expression of reporter genes. We then validated that NUTRIREG can be used in human T cells to transiently express a therapeutic gene such as IL-10. Overall, our results represent a solid basis for the promising use of NUTRIREG to regulate transgene expression in human T cells in a reversible way, and more generally for numerous preventive or curative therapeutic possibilities in cellular immunotherapy strategies.
Keyphrases
- gene expression
- stem cell transplantation
- endothelial cells
- poor prognosis
- cell therapy
- amino acid
- dna methylation
- induced pluripotent stem cells
- pluripotent stem cells
- high dose
- stem cells
- genome wide
- mesenchymal stem cells
- transcription factor
- bone marrow
- long non coding rna
- rectal cancer
- endoplasmic reticulum stress