| Literature DB >> 23559898 |
Young-Ran Lee1, Young-Hee Lee, Ki-Hyang Kim, Sun-A Im, Chong-Kil Lee.
Abstract
Previously we showed that biodegradable nanoparticles containing poly-IC or CpG oligodeoxynucleotide (ODN) together with ovalbumin (OVA) were efficient at inducing MHC-restricted presentation of OVA peptides in dendritic cells. The CTL-inducing activities of the nanoparticles were examined in the present study. Nanoparticles containing poly-IC or CpG ODN together with OVA were prepared using biodegradable polymer poly(D,L-lactic acid-co-glycolic acid), and then were opsonized with mouse IgG. The nanoparticles were injected into the tail vein of mice, and 7 days later the OVA-specific CTL activities were measured using an in vivo CTL assay. Immunization of mice with the nanoparticles containing poly-IC or CpG ODN together with OVA elicited potent OVA-specific CTL activity compared to those containing OVA only. In accordance with these results, nanoparticles containing poly-IC or CpG ODN together with OVA exerted potent antitumor activity in mice that were subcutaneously implanted with EG7.OVA tumor cells. These results show that encapsulation of poly-IC or CpG ODN together with antigen in biodegradable nanoparticles is an effective approach for the induction of potent antigen-specific CTL responses in vivo.Entities:
Keywords: Antitumor activity; CTL; CpG; Nanoparticle; PLGA; Poly-IC
Year: 2013 PMID: 23559898 PMCID: PMC3607708 DOI: 10.4110/in.2013.13.1.30
Source DB: PubMed Journal: Immune Netw ISSN: 1598-2629 Impact factor: 6.303