Prolonged intratumoral treatment with TLR7/8 agonist R848 regulates the tumor immune microenvironment resulting in enhanced antitumor activity
BACKGROUND: Toll-like receptor 7/8 agonists (TLR7/8a), such as resiquimod (R848), are highly potent in activating dendritic cells and thus hold promise for T cell-mediated tumor immunotherapies. However, the short half-life of these small molecules in the lesion and the associated systemic immunotoxicity post-leakage of the drug into the circulation make their clinical application challenging. MATERIALS: To overcome these shortcomings, we tested prolonged TLR7/8a therapy by intratumoral infusion of R848 for 25 h using a micropump to achieve durable therapeutic effects while minimizing the proinflammatory cytokine levels in the plasma post leakage of the drug into the circulation. RESULTS: < 0.05), indicating efficient activation of local and abscopal immunity by prolonged therapy with R848. Furthermore, the R848 functional concentration assay demonstrated that the micropump prolonged the treatment time of R848 drugs in tumors and reduced the requirement for higher doses, enhancing safety. CONCLUSION: Taken together, this study provides new insights into TLR7/8a immunotherapy for improved clinical performance, with potential benefits for patients with superficial tumors amenable to prolonged intratumoral infusion via micropump.
Authors
- X N Zhang
- Xueyi Sun
- Shaoxuan Wu
- Hang Gu
- Hongwen Li (ORCID: https://orcid.org/0000-0003-0316-6500)
- M Zhang
- Meng Dong
- Yue Zhang
- Zeyuan Wang
- Siyu Qian
- Huitao Liu
- Zhiqiang Han
- Fengyun Xing
- Shixuan Cheng
- Zhenzhen Yang
- Qingjiang Chen (ORCID: https://orcid.org/0000-0003-0025-7554)
- Na Wan
Institutions
- Henan University of Technology (CN)
- Henan Academy of Sciences (CN)
- Henan University of Engineering (CN)
- Office of International Affairs (US)
- First Affiliated Hospital of Zhengzhou University (CN)
Publication Details
- Journal
- Cancer Biology & Therapy
- Published
- 2026-05-12
- DOI
- https://doi.org/10.1080/15384047.2026.2670801
- Primary Topic
- Immunotherapy and Immune Responses
- Type
- article
- Field-Weighted Citation Impact
- 0.00