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Emerging nanoparticle platforms for CpG oligonucleotide delivery.
Li, Mingqiang; Yao, Haochen; Yi, Ke; Lao, Yeh-Hsing; Shao, Dan; Tao, Yu.
Affiliation
  • Li M; Laboratory of Biomaterials and Translational Medicine, Center for Nanomedicine, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China. taoy28@mail.sysu.edu.cn.
  • Yao H; Hepatobiliary and Pancreatic Surgery Department, General Surgery Center, First Hospital of Jilin University, No. 1 Xinmin Street, Changchun, 130021, Jilin, China.
  • Yi K; Laboratory of Biomaterials and Translational Medicine, Center for Nanomedicine, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China. taoy28@mail.sysu.edu.cn.
  • Lao YH; Department of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY, 14214, USA.
  • Shao D; Institutes of Life Sciences, School of Biomedical Sciences and Engineering, South China University of Technology, Guangzhou, China.
  • Tao Y; Laboratory of Biomaterials and Translational Medicine, Center for Nanomedicine, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China. taoy28@mail.sysu.edu.cn.
Biomater Sci ; 12(9): 2203-2228, 2024 Apr 30.
Article in En | MEDLINE | ID: mdl-38293828
ABSTRACT
Unmethylated cytosine-phosphate-guanine (CpG) oligodeoxynucleotides (ODNs), which were therapeutic DNA with high immunostimulatory activity, have been applied in widespread applications from basic research to clinics as therapeutic agents for cancer immunotherapy, viral infection, allergic diseases and asthma since their discovery in 1995. The major factors to consider for clinical translation using CpG motifs are the protection of CpG ODNs from DNase degradation and the delivery of CpG ODNs to the Toll-like receptor-9 expressed human B-cells and plasmacytoid dendritic cells. Therefore, great efforts have been devoted to the advances of efficient delivery systems for CpG ODNs. In this review, we outline new horizons and recent developments in this field, providing a comprehensive summary of the nanoparticle-based CpG delivery systems developed to improve the efficacy of CpG-mediated immune responses, including DNA nanostructures, inorganic nanoparticles, polymer nanoparticles, metal-organic-frameworks, lipid-based nanosystems, proteins and peptides, as well as exosomes and cell membrane nanoparticles. Moreover, future challenges in the establishment of CpG delivery systems for immunotherapeutic applications are discussed. We expect that the continuously growing interest in the development of CpG-based immunotherapy will certainly fuel the excitement and stimulation in medicine research.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligodeoxyribonucleotides / Nanoparticles Limits: Animals / Humans Language: En Journal: Biomater Sci Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligodeoxyribonucleotides / Nanoparticles Limits: Animals / Humans Language: En Journal: Biomater Sci Year: 2024 Document type: Article Affiliation country: China