Cargando…
Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy
Dendritic cells (DCs) are potent professional antigen-presenting cells that are capable of initiating a primary immune response and activating T cells, and they play a pivotal role in the immune responses of the host to cancer. Prior to antigen presentation, efficient antigen and adjuvant uptake by...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098754/ https://www.ncbi.nlm.nih.gov/pubmed/27843314 http://dx.doi.org/10.2147/IJN.S109001 |
_version_ | 1782465820874506240 |
---|---|
author | Han, Hee Dong Byeon, Yeongseon Kang, Tae Heung Jung, In Duk Lee, Jeong-Won Shin, Byung Cheol Lee, Young Joo Sood, Anil K Park, Yeong-Min |
author_facet | Han, Hee Dong Byeon, Yeongseon Kang, Tae Heung Jung, In Duk Lee, Jeong-Won Shin, Byung Cheol Lee, Young Joo Sood, Anil K Park, Yeong-Min |
author_sort | Han, Hee Dong |
collection | PubMed |
description | Dendritic cells (DCs) are potent professional antigen-presenting cells that are capable of initiating a primary immune response and activating T cells, and they play a pivotal role in the immune responses of the host to cancer. Prior to antigen presentation, efficient antigen and adjuvant uptake by DCs is necessary to induce their maturation and cytokine generation. Nanoparticles (NPs) are capable of intracellular delivery of both antigen and adjuvant to DCs. Here, we developed an advanced poly(d,l-lactide-co-glycolide) (PLGA)-NP encapsulating both ovalbumin (OVA) as a model antigen and polyinosinic-polycytidylic acid sodium salt (Toll-like receptor 3 ligand) as an adjuvant to increase intracellular delivery and promote DC maturation. The PLGA-NPs were taken up by DCs, and their uptake greatly facilitated major histocompatibility class I antigen presentation in vitro. Moreover, vaccination with PLGA-NP-treated DCs led to the generation of ovalbumin-specific CD8(+) T cells, and the resulting antitumor efficacy was significantly increased in EG.7 and TC-1 tumor-bearing mice compared to control mice (P<0.01). Taken together, these findings demonstrated that the PLGA-NP platform may be an effective method for delivering tumor-specific antigens or adjuvants to DCs. |
format | Online Article Text |
id | pubmed-5098754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50987542016-11-14 Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy Han, Hee Dong Byeon, Yeongseon Kang, Tae Heung Jung, In Duk Lee, Jeong-Won Shin, Byung Cheol Lee, Young Joo Sood, Anil K Park, Yeong-Min Int J Nanomedicine Original Research Dendritic cells (DCs) are potent professional antigen-presenting cells that are capable of initiating a primary immune response and activating T cells, and they play a pivotal role in the immune responses of the host to cancer. Prior to antigen presentation, efficient antigen and adjuvant uptake by DCs is necessary to induce their maturation and cytokine generation. Nanoparticles (NPs) are capable of intracellular delivery of both antigen and adjuvant to DCs. Here, we developed an advanced poly(d,l-lactide-co-glycolide) (PLGA)-NP encapsulating both ovalbumin (OVA) as a model antigen and polyinosinic-polycytidylic acid sodium salt (Toll-like receptor 3 ligand) as an adjuvant to increase intracellular delivery and promote DC maturation. The PLGA-NPs were taken up by DCs, and their uptake greatly facilitated major histocompatibility class I antigen presentation in vitro. Moreover, vaccination with PLGA-NP-treated DCs led to the generation of ovalbumin-specific CD8(+) T cells, and the resulting antitumor efficacy was significantly increased in EG.7 and TC-1 tumor-bearing mice compared to control mice (P<0.01). Taken together, these findings demonstrated that the PLGA-NP platform may be an effective method for delivering tumor-specific antigens or adjuvants to DCs. Dove Medical Press 2016-11-02 /pmc/articles/PMC5098754/ /pubmed/27843314 http://dx.doi.org/10.2147/IJN.S109001 Text en © 2016 Han et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Han, Hee Dong Byeon, Yeongseon Kang, Tae Heung Jung, In Duk Lee, Jeong-Won Shin, Byung Cheol Lee, Young Joo Sood, Anil K Park, Yeong-Min Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy |
title | Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy |
title_full | Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy |
title_fullStr | Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy |
title_full_unstemmed | Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy |
title_short | Toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy |
title_sort | toll-like receptor 3-induced immune response by poly(d,l-lactide-co-glycolide) nanoparticles for dendritic cell-based cancer immunotherapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098754/ https://www.ncbi.nlm.nih.gov/pubmed/27843314 http://dx.doi.org/10.2147/IJN.S109001 |
work_keys_str_mv | AT hanheedong tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT byeonyeongseon tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT kangtaeheung tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT junginduk tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT leejeongwon tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT shinbyungcheol tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT leeyoungjoo tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT soodanilk tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy AT parkyeongmin tolllikereceptor3inducedimmuneresponsebypolydllactidecoglycolidenanoparticlesfordendriticcellbasedcancerimmunotherapy |