A Light Responsive Nanoparticle-Based Delivery System Using Pheophorbide A Graft Polyethylenimine for Dendritic Cell-Based Cancer Immunotherapy.

Citation data:

Molecular pharmaceutics, ISSN: 1543-8392, Vol: 14, Issue: 5, Page: 1760-1770

Publication Year:
2017
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PMID:
28296410
DOI:
10.1021/acs.molpharmaceut.7b00015
Author(s):
Zhang, Chuangnian, Zhang, Ju, Shi, Gaona, Song, Huijuan, Shi, Shengbin, Zhang, Xiuyuan, Huang, Pingsheng, Wang, Zhihong, Wang, Weiwei, Wang, Chun, Kong, Deling, Li, Chen Show More Hide
Publisher(s):
American Chemical Society (ACS)
Tags:
Biochemistry, Genetics and Molecular Biology, Pharmacology, Toxicology and Pharmaceutics
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article description
In this study, the photochemical internalization (PCI) technique was adopted in a nanoparticle-based antigen delivery system to enhance antigen-specific CD8 T cell immune response for cancer immunotherapy. Pheophorbide A, a hydrophobic photosensitizer, grafted with polyethylenimine (PheoA-PEI) with endosome escape activity and near-infrared imaging capability was prepared. A model antigen ovalbumin (OVA) was then complexed with PheoA-PEI to form PheoA-PEI/OVA nanoparticles (PheoA-PEI/OVA NPs) that are responsive to light. Flow cytometry analysis revealed increased endocytosis in a murine dendritic cell line (DC2.4) that was treated with PheoA-PEI/OVA NPs compared to free OVA. Generation of reactive oxygen species (ROS) in DC2.4 cells was also confirmed quantitatively and qualitatively using 2',7'-dichlorodihydrofluorescein diacetate (DCFH-DA). Confocal laser scanning microscopy (CLSM) further demonstrated that the PheoA-PEI/OVA NPs enhanced cytosolic antigen release after light stimulation. Moreover, PheoA-PEI/OVA NP treated DC2.4 cells exhibited enhanced cross-presentation to B3Z T cell hybridoma in vitro after light irradiation, substantially increased compared to those treated with free OVA. Consistently, in vivo results revealed upregulation of CD3CD8T lymphocytes in tumors of mice treated with dendritic cells plus PheoA-PEI/OVA NPs and light irradiation. The activated T cell response is partly responsible for the inhibitory effect on E.G7 tumor growth in mice immunized with dendritic cells plus PheoA-PEI/OVA NPs and light irradiation. Our results demonstrate the feasibility to enhance antigen-specific CD8 T cell immune response by light-responsive nanoparticle-based vaccine delivery for cancer immunotherapy.

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