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Updated: Apr 24, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Engineering antibody-armed oncolytic viruses: design strategies, synergistic mechanisms, and clinical translation
Xiaozhen Kang1, Xue Yang2, Hui Wu3
1Zhejiang Key Laboratory of Zero Magnetic Medicine, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou, Zhejiang, China.
Abstract:
Therapeutic antibodies are widely used in cancer biotherapy due to their target specificity, mediating tumor cell inhibition, angiogenesis suppression, and immune modulation. However, systemic administration often leads to off-target effects, as many antibody targets are also expressed in normal tissues, limiting intratumoral drug concentration and causing adverse events. Oncolytic viruses (OVs), which selectively infect and lyse tumor cells while activating host anti-tumor immunity, offer a promising platform for localized antibody delivery. Their inherent tumor tropism, intratumoral administration, and high genetic manipulability enable the engineering of OVs to express exogenous antibodies within the tumor microenvironment, enhancing therapeutic specificity and synergizing oncolytic and immune-mediated effects. In this review, we summarize the biological properties of OVs, strategies for engineering antibody payloads, the mechanistic interplay between OV-induced oncolysis and immune modulation, and current challenges and opportunities for clinical translation. By integrating these aspects, we provide insights into optimizing OV-based antibody therapies for enhanced tumor-targeted efficacy and reduced systemic toxicity.
Insights
Oncolytic viruses (OVs) can be engineered to deliver therapeutic antibodies directly to tumors, enhancing cancer treatment specificity. This approach aims to improve efficacy and reduce side effects associated with traditional antibody therapies.
Area of Science:
- Biotechnology
- Immunotherapy
- Oncology
Background:
- Therapeutic antibodies are crucial for cancer treatment but cause systemic toxicity due to off-target effects.
- Oncolytic viruses (OVs) selectively target and destroy tumor cells, offering a potential solution for localized drug delivery.
Purpose of the Study:
- To review the use of oncolytic viruses for engineered antibody delivery in cancer therapy.
- To explore strategies for enhancing tumor-specific antibody expression and synergistic therapeutic effects.
Main Methods:
- Review of biological properties of OVs.
- Analysis of strategies for engineering OV antibody payloads.
- Examination of the interplay between OV-induced oncolysis and anti-tumor immunity.
Main Results:
- OVs enable localized antibody expression within the tumor microenvironment.
- Engineered OVs enhance therapeutic specificity and combine oncolytic and immune-mediated effects.
- This approach promises improved tumor-targeted efficacy and reduced systemic toxicity.
Conclusions:
- Oncolytic virus-mediated antibody delivery is a promising strategy for cancer biotherapy.
- Optimizing OV engineering and understanding OV-immune interplay are key for clinical translation.
- This approach offers potential for more effective and safer cancer treatments.
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