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Evaluation of the Elements of Short Hairpin RNAs in Developing shRNA-Containing CAR T Cells.

Ryan UrakBrenna GittinsCitradewi SoemardyNicole GrepoLior GoldbergMadeleine MakerGalina ShevchenkoAlicia DavisShirley LiTristan A ScottKevin V MorrisStephen J FormanXiuli Wang
Published in: Cancers (2023)
Short hairpin RNAs (shRNAs) have emerged as a powerful tool for gene knockdown in various cellular systems, including chimeric antigen receptor (CAR) T cells. However, the elements of shRNAs that are crucial for their efficacy in developing shRNA-containing CAR T cells remain unclear. In this study, we evaluated the impact of different shRNA elements, including promoter strength, orientation, multiple shRNAs, self-targeting, and sense and antisense sequence composition on the knockdown efficiency of the target gene in CAR T cells. Our findings highlight the importance of considering multiple shRNAs and their orientation to achieve effective knockdown. Moreover, we demonstrate that using a strong promoter and avoiding self-targeting can enhance CAR T cell functionality. These results provide a framework for the rational design of CAR T cells with shRNA-mediated knockdown capabilities, which could improve the therapeutic efficacy of CAR T cell-based immunotherapy.
Keyphrases
  • dna methylation
  • gene expression
  • transcription factor
  • copy number