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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.
Afiliação
  • Han HD; Department of Immunology, School of Medicine, Konkuk University, Chungwondaero, Chungju-Si, Chungcheongbuk-Do.
  • Byeon Y; Department of Immunology, School of Medicine, Konkuk University, Chungwondaero, Chungju-Si, Chungcheongbuk-Do.
  • Kang TH; Department of Immunology, School of Medicine, Konkuk University, Chungwondaero, Chungju-Si, Chungcheongbuk-Do.
  • Jung ID; Department of Immunology, School of Medicine, Konkuk University, Chungwondaero, Chungju-Si, Chungcheongbuk-Do.
  • Lee JW; Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul.
  • Shin BC; Bio/Drug Discovery Division, Korea Research Institute of Chemical Technology, Yuseong-gu, Daejeon.
  • Lee YJ; Department of Bioscience and Biotechnology, Sejong University, Kwang-Jin-Gu, Seoul, South Korea.
  • Sood AK; Department of Gynecologic Oncology and Reproductive Medicine; Department of Cancer Biology; Center for RNA Interference and Non-coding RNA, The University of Texas MD Anderson Cancer Center, TX, USA.
  • Park YM; Department of Immunology, School of Medicine, Konkuk University, Chungwondaero, Chungju-Si, Chungcheongbuk-Do.
Int J Nanomedicine ; 11: 5729-5742, 2016.
Article em En | MEDLINE | ID: mdl-27843314
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido Poliglicólico / Timoma / Células Dendríticas / Ácido Láctico / Receptor 3 Toll-Like / Nanopartículas / Imunoterapia / Neoplasias Experimentais Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido Poliglicólico / Timoma / Células Dendríticas / Ácido Láctico / Receptor 3 Toll-Like / Nanopartículas / Imunoterapia / Neoplasias Experimentais Idioma: En Ano de publicação: 2016 Tipo de documento: Article