Cargando…

Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist

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 pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Young-Ran, Lee, Young-Hee, Kim, Ki-Hyang, Im, Sun-A, Lee, Chong-Kil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607708/
https://www.ncbi.nlm.nih.gov/pubmed/23559898
http://dx.doi.org/10.4110/in.2013.13.1.30
_version_ 1782264127856574464
author Lee, Young-Ran
Lee, Young-Hee
Kim, Ki-Hyang
Im, Sun-A
Lee, Chong-Kil
author_facet Lee, Young-Ran
Lee, Young-Hee
Kim, Ki-Hyang
Im, Sun-A
Lee, Chong-Kil
author_sort Lee, Young-Ran
collection PubMed
description 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.
format Online
Article
Text
id pubmed-3607708
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher The Korean Association of Immunologists
record_format MEDLINE/PubMed
spelling pubmed-36077082013-04-04 Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist Lee, Young-Ran Lee, Young-Hee Kim, Ki-Hyang Im, Sun-A Lee, Chong-Kil Immune Netw Brief Communication 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. The Korean Association of Immunologists 2013-02 2013-02-28 /pmc/articles/PMC3607708/ /pubmed/23559898 http://dx.doi.org/10.4110/in.2013.13.1.30 Text en Copyright © 2013 The Korean Association of Immunologists http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Communication
Lee, Young-Ran
Lee, Young-Hee
Kim, Ki-Hyang
Im, Sun-A
Lee, Chong-Kil
Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist
title Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist
title_full Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist
title_fullStr Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist
title_full_unstemmed Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist
title_short Induction of Potent Antigen-specific Cytotoxic T Cell Response by PLGA-nanoparticles Containing Antigen and TLR Agonist
title_sort induction of potent antigen-specific cytotoxic t cell response by plga-nanoparticles containing antigen and tlr agonist
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607708/
https://www.ncbi.nlm.nih.gov/pubmed/23559898
http://dx.doi.org/10.4110/in.2013.13.1.30
work_keys_str_mv AT leeyoungran inductionofpotentantigenspecificcytotoxictcellresponsebyplgananoparticlescontainingantigenandtlragonist
AT leeyounghee inductionofpotentantigenspecificcytotoxictcellresponsebyplgananoparticlescontainingantigenandtlragonist
AT kimkihyang inductionofpotentantigenspecificcytotoxictcellresponsebyplgananoparticlescontainingantigenandtlragonist
AT imsuna inductionofpotentantigenspecificcytotoxictcellresponsebyplgananoparticlescontainingantigenandtlragonist
AT leechongkil inductionofpotentantigenspecificcytotoxictcellresponsebyplgananoparticlescontainingantigenandtlragonist