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Updated: Aug 24, 2025

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
Published on: February 21, 2025
Emerging frontiers in immuno- and gene therapy for cancer
Michael P Gustafson1, John A Ligon2, Alexey Bersenev3
1Immuno-Gene Therapy Committee, International Society for Cell and Gene Therapy; Department of Laboratory Medicine and Pathology, Mayo Clinic in Arizona, Phoenix, Arizona, USA.
Background Aims:
The field of cell and gene therapy in oncology has moved rapidly since 2017 when the first cell and gene therapies, Kymriah followed by Yescarta, were approved by the Food and Drug Administration in the United States, followed by multiple other countries. Since those approvals, several new products have gone on to receive approval for additional indications. Meanwhile, efforts have been made to target different cancers, improve the logistics of delivery and reduce the cost associated with novel cell and gene therapies. Here, we highlight various cell and gene therapy-related technologies and advances that provide insight into how these new technologies will speed the translation of these therapies into the clinic.
Conclusions:
In this review, we provide a broad overview of the current state of cell and gene therapy-based approaches for cancer treatment - discussing various effector cell types and their sources, recent advances in both CAR and non-CAR genetic modifications, and highlighting a few promising approaches for increasing in vivo efficacy and persistence of therapeutic drug products.
Insights
Cell and gene therapies have advanced significantly since 2017, with new approvals and ongoing research to improve cancer treatment. This review explores technologies accelerating the clinical translation of these innovative oncology therapies.
Area of Science:
- Oncology
- Cell Therapy
- Gene Therapy
Background:
- The oncology field has seen rapid advancements in cell and gene therapies since 2017.
- Multiple products have gained approval for various indications, expanding treatment options.
- Ongoing efforts focus on targeting diverse cancers, optimizing delivery, and reducing costs.
Approach:
- This review provides an overview of current cell and gene therapy approaches in cancer treatment.
- It discusses various effector cell types and their sources.
- Recent advances in CAR and non-CAR genetic modifications are highlighted.
Key Points:
- Exploration of novel cell and gene therapy technologies.
- Focus on improving in vivo efficacy and persistence of therapeutic products.
- Strategies to accelerate clinical translation of these therapies.
Conclusions:
- Cell and gene therapies represent a rapidly evolving area in oncology.
- Advances in genetic modification and effector cell strategies are crucial.
- Continued innovation is key to expanding the clinical application of these treatments.
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