Engineering Strategies to Enhance TCR-Based Adoptive T Cell Therapy.
Jan A RathCaroline ArberPublished in: Cells (2020)
T cell receptor (TCR)-based adoptive T cell therapies (ACT) hold great promise for the treatment of cancer, as TCRs can cover a broad range of target antigens. Here we summarize basic, translational and clinical results that provide insight into the challenges and opportunities of TCR-based ACT. We review the characteristics of target antigens and conventional αβ-TCRs, and provide a summary of published clinical trials with TCR-transgenic T cell therapies. We discuss how synthetic biology and innovative engineering strategies are poised to provide solutions for overcoming current limitations, that include functional avidity, MHC restriction, and most importantly, the tumor microenvironment. We also highlight the impact of precision genome editing on the next iteration of TCR-transgenic T cell therapies, and the discovery of novel immune engineering targets. We are convinced that some of these innovations will enable the field to move TCR gene therapy to the next level.
Keyphrases
- cell therapy
- regulatory t cells
- genome editing
- crispr cas
- dendritic cells
- gene therapy
- clinical trial
- stem cells
- mesenchymal stem cells
- small molecule
- squamous cell carcinoma
- randomized controlled trial
- high throughput
- big data
- immune response
- artificial intelligence
- binding protein
- squamous cell
- combination therapy
- smoking cessation