# Advances of oncolytic vaccinia viruses armed with interleukin in tumor therapy

**Authors:** Mingyong Zha, Fei Huang, Songlin Li, Qi Wang, Yong Tang

PMC · DOI: 10.3389/fonc.2025.1594621 · Frontiers in Oncology · 2025-05-21

## TL;DR

This paper explores how vaccinia viruses modified with interleukins can improve cancer treatment by boosting the immune response and combining with other therapies.

## Contribution

The paper introduces novel combinatorial strategies and solutions to immune clearance challenges in oncolytic vaccinia virus therapy.

## Key findings

- Armed vaccinia viruses enhance immune cell infiltration and suppress immunosuppressive elements in tumors.
- Combinatorial therapies with checkpoint inhibitors and metabolic modulators improve treatment outcomes.
- Strategies like polymer encapsulation and AI-driven designs are proposed to optimize virus delivery and efficacy.

## Abstract

Oncolytic vaccinia viruses armed with interleukins represent a promising frontier in tumor therapy. Oncolytic vaccinia viruses express IL-2, IL-10, IL-12, IL-15, IL-21, IL-23, IL-24, and IL-36γ remodel the tumor microenvironment,enhance immune cell infiltration, suppress immunosuppressive elements and promot systemic antitumor immunity. Combinatorial strategies with chemotherapy, radiotherapy, metabolic modulators, immune checkpoint inhibitors, or natural compounds amplify therapeutic efficacy for tumors. In addition, we review the existing solutions to the problems of the immune clearance of virus, such as the use of inhibitors to prevent neutralizing antibodies from binding to the virus and the use of polymer encapsulation or mesenchymal stem cell loading. We also discussed Current directions include optimizing delivery systems, leveraging Artificial Intelligence for personalized designs of Oncolytic vaccinia virus inserted interleukins to guide the research in the future.

## Linked entities

- **Proteins:** IL2 (interleukin 2), IL10 (interleukin 10), IL12 (Interleukin 12 level), IL15 (interleukin 15), IL21 (interleukin 21), IL37 (interleukin 37), IL24 (interleukin 24), IL36G (interleukin 36 gamma)
- **Diseases:** tumor (MONDO:0005070), cancer (MONDO:0004992)

## Full-text entities

- **Genes:** IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL21 (interleukin 21) [NCBI Gene 59067] {aka CVID11, IL-21, Za11}, IL24 (interleukin 24) [NCBI Gene 11009] {aka C49A, FISP, IL10B, MDA7, MOB5, ST16}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}
- **Diseases:** tumor (MESH:D009369)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12133479/full.md

## References

177 references — full list in the complete paper: https://tomesphere.com/paper/PMC12133479/full.md

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Source: https://tomesphere.com/paper/PMC12133479