Lentiviral vectors in cancer immunotherapy
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Updated: Apr 15, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Robyn Aa Oldham1, Elliot M Berinstein, Jeffrey A Medin
1Department of Medical Biophysics, University of Toronto, 27 King's College Circle, Toronto, ON M5S, Canada.
Abstract:
Basic science advances in cancer immunotherapy have resulted in various treatments that have recently shown success in the clinic. Many of these therapies require the insertion of genes into cells to directly kill them or to redirect the host's cells to induce potent immune responses. Other analogous therapies work by modifying effector cells for improved targeting and enhanced killing of tumor cells. Initial studies done using γ-retroviruses were promising, but safety concerns centered on the potential for insertional mutagenesis have highlighted the desire to develop other options for gene delivery. Lentiviral vectors (LVs) have been identified as potentially more effective and safer alternative delivery vehicles. LVs are now in use in clinical trials for many different types of inherited and acquired disorders, including cancer. This review will discuss current knowledge of LVs and the applications of this viral vector-based delivery vehicle to cancer immunotherapy.
Insights
Lentiviral vectors offer a safer and more effective gene delivery method for cancer immunotherapy. These viral vectors are being explored in clinical trials for various cancers, improving targeted cell modification and immune responses.
Area of Science:
- Oncology
- Immunology
- Gene Therapy
- Virology
Background:
- Cancer immunotherapy has advanced significantly, with gene-based therapies showing clinical success.
- Current gene therapies often involve direct gene insertion for cell killing or immune stimulation.
- Early gene delivery methods using gamma-retroviruses raised safety concerns due to insertional mutagenesis.
Purpose of the Study:
- To review current knowledge on lentiviral vectors (LVs).
- To discuss the application of LVs in cancer immunotherapy.
- To highlight LVs as a safer alternative for gene delivery in cancer treatment.
Main Methods:
- Review of existing scientific literature on lentiviral vectors and cancer immunotherapy.
- Analysis of clinical trial data and research findings related to LV applications.
- Discussion of the mechanisms and safety profiles of LVs compared to other vectors.
Main Results:
- Lentiviral vectors are identified as a promising alternative to gamma-retroviruses for gene delivery.
- LVs demonstrate potential for safer and more effective gene insertion.
- LVs are currently utilized in clinical trials for diverse disorders, including cancer.
Conclusions:
- Lentiviral vectors represent a significant advancement in gene delivery for cancer immunotherapy.
- Their improved safety and efficacy profile make them suitable for clinical applications.
- Further research and clinical trials are expected to expand the role of LVs in treating cancer.
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