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Non-Viral Engineering of Primary Human T Cells via Homology-Mediated End-Joining Targeted Integration of Large DNA Templates
Published on: May 9, 2025
464
Emerging Strategies in TCR-Engineered T Cells
Fang Wei1, Xiao-Xia Cheng1, John Zhao Xue1
1Genetic Engineering Laboratory, School of Biological & Environmental Engineering, Xi'An University, Xi'An, China.
Frontiers in Immunology
|April 18, 2022
Summary
T-cell receptor (TCR)-engineered T cells (TCR-T) show promise for cancer immunotherapy by targeting intracellular tumor antigens. Combining TCR-T with neoantigen vaccines and checkpoint blockade may enhance efficacy against solid tumors.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Adoptive cell transfer (ACT) immunotherapies, including CAR-T and TCR-T, have advanced cancer treatment.
- TCR-T cells recognize intracellular and cell-surface tumor antigens, including neoantigens, at lower concentrations than CAR-T cells.
Purpose of the Study:
- To review current challenges and opportunities in TCR-T therapy.
- To outline strategies for improving TCR-T efficacy, particularly for solid tumors.
Main Methods:
- Review of basic, translational, and clinical research on TCR-T therapy.
- Analysis of emerging ACT strategies and limitations.
- Proposal of a combination therapy approach.
Main Results:
- TCR-T therapy offers potential for treating various human cancers due to its sensitivity and broad target recognition.
- Targeting tumor-specific neoantigens is crucial for effective cancer immunotherapy.
- A combination strategy involving neoantigen vaccines, checkpoint blockade, and neoantigen-specific TCR-T is proposed.
Conclusions:
- TCR-T therapy holds significant promise for cancer treatment, especially for solid tumors.
- Combining neoantigen vaccines, checkpoint blockade, and TCR-T offers a potential strategy for a tumor-specific therapy.
- This integrated approach may improve cancer immunotherapy outcomes and provide a general strategy for eradicating multiple cancers.
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