Image-guided in situ cancer vaccination with combination of multi-functional nano-adjuvant and an irreversible electroporation technique
- Authors
- Han, Jun-Hyeok; Lee, Yun Young; Shin, Ha Eun; Han, Jieun; Kang, Jeon Min; Wang, Chi-Pin James; Park, Jung-Hoon; Kim, Se-Na; Yoon, Jong-Hwi; Kwon, Ho-Keun; Park, Dae-Hwan; Park, Tae-Eun; Choy, Young Bin; Kim, Dong-Hyun; Kim, Tae-Hyung; Min, Junhong; Kim, Ik-Hwan; Park, Chun Gwon; Han, Dong Keun; Park, Wooram
- Issue Date
- 10월-2022
- Publisher
- ELSEVIER SCI LTD
- Keywords
- Cancer immunotherapy; Multi-functional nano-adjuvant; Irreversible electroporation; Image-guided cancer therapy
- Citation
- BIOMATERIALS, v.289
- Indexed
- SCIE
SCOPUS
- Journal Title
- BIOMATERIALS
- Volume
- 289
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/146570
- DOI
- 10.1016/j.biomaterials.2022.121762
- ISSN
- 0142-9612
- Abstract
- Cancer immunotherapy is a next-generation treatment strategy; however, its side effects limit its clinical translation. Here, a novel combination of a multi-functional nano-adjuvant (M-NA) prepared with an iron oxide/ gold core and a cationic polymer shell via multilayer synthesis with CpG oligodeoxynucleotide (CpG-ODN) electrostatically complexed on its surface, and irreversible electroporation (IRE) technique was developed for effective image-guided in situ cancer vaccination. The M-NA can be retained long-term in the dense tumoral extracellular matrix after intratumoral injection and internalized by antigen-presenting cells (APCs). The IRE can induce immunogenic cell death. Indeed, in a mouse tumor model, the M-NA showed longer tumor retention time than free CpG-ODN. Compared with other treatments, the combined treatment significantly inhibited tumor growth with 100% survival rate for-60 days. The therapy induced the activation of cytotoxic lymphocytes and the maturation of APCs in vivo. This treatment could be effective in image-guided local cancer immunotherapy.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Graduate School > Department of Life Sciences > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.