A Virus-Mimicking Nucleic Acid Nanogel Reprograms Microglia and Macrophages for Glioblastoma Therapy.

Abstract

Immunotherapy is recognized as one of the most promising approaches to treat cancers. However, its effect in glioblastoma (GBM) treatment is insufficient, which can in part be attributed to the immunosuppressive tumor microenvironment (TME). Microglia and macrophages are the main immune infiltrating cells in the TME of GBM. Unfortunately, instead of initiating the anti-tumor response, GBM-infiltrating microglia and macrophages switch to a tumor-promoting phenotype (M2), and support tumor growth, angiogenesis, and immunosuppression by the release of cytokines. In this work, a virus-mimicking membrane-coated nucleic acid nanogel Vir-Gel embedded with therapeutic miRNA is developed, which can reprogram microglia and macrophages from a pro-invasive M2 phenotype to an anti-tumor M1 phenotype. By mimicking the virus infection process, Vir-Gel significantly enhances the targetability and cell uptake efficiency of the miR155-bearing nucleic acid nanogel. In vivo evaluations demonstrate that Vir-Gel apparently prolongs the circulation lifetime of miR155 and endows it with an active tumor-targeting capability and excellent tumor inhibition efficacy. Owing to its noninvasive feature and effective delivery capability, the virus-mimicking nucleic acid nanogel provides a general and convenient platform that can successfully treat a wide range of diseases.

• Authors: Xihui Gao, Sha Li, Fei Ding, Xinlong Liu, Yijing Wu, Jing Li, Jing Feng, Xinyuan Zhu, Chuan Zhang
• Journal: Advanced materials (Deerfield Beach, Fla.) (Adv Mater) Vol. 33 Issue 9 Pg. e2006116 (Mar 2021) ISSN: 1521-4095 [Electronic] Germany
• PMID: 33501743 (Publication Type: Journal Article)
• Copyright: © 2021 Wiley-VCH GmbH.

Chemical References

• Cytokines
• Delayed-Action Preparations
• Immunologic Factors
• MicroRNAs
• Nanogels

Topics

• Animals
• Apoptosis
• Biological Transport
• Biomimetic Materials (chemistry)
• Cell Line, Tumor
• Cell Proliferation
• Cytokines (metabolism)
• Delayed-Action Preparations (chemistry)
• Glioblastoma (therapy)
• Humans
• Immunologic Factors (metabolism)
• Immunotherapy
• Macrophages (chemistry)
• Mice
• MicroRNAs (chemistry)
• Microglia (chemistry)
• Nanogels (chemistry)
• Neovascularization, Pathologic (metabolism)
• Tumor Microenvironment