Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep15262
Title: Antigenically Modified Human Pluripotent Stem Cells Generate Antigen-Presenting Dendritic Cells
Authors: Zeng, J
Wu, C
Wang, S 
Keywords: cancer vaccine
epitope
melan A
tumor antigen
CD8+ T lymphocyte
cell line
cytology
dendritic cell
DNA responsive element
gene vector
genetics
human
immunocompetence
immunology
metabolism
Neoplasms
pluripotent stem cell
reporter gene
Antigens, Neoplasm
Cancer Vaccines
CD8-Positive T-Lymphocytes
Cell Line
Dendritic Cells
Epitopes
Genes, Reporter
Genetic Vectors
Humans
Immunocompetence
MART-1 Antigen
Neoplasms
Pluripotent Stem Cells
Response Elements
Issue Date: 2015
Citation: Zeng, J, Wu, C, Wang, S (2015). Antigenically Modified Human Pluripotent Stem Cells Generate Antigen-Presenting Dendritic Cells. Scientific Reports 5 : 15262. ScholarBank@NUS Repository. https://doi.org/10.1038/srep15262
Rights: Attribution 4.0 International
Abstract: Human pluripotent stem cells (hPSCs) provide a promising platform to produce dendritic cell (DC) vaccine. To streamline the production process, we investigated a unique antigen-loading strategy that suits this novel platform. Specifically, we stably modified hPSCs using tumour antigen genes in the form of a full-length tumour antigen gene or an artificial tumour antigen epitope-coding minigene. Such antigenically modified hPSCs were able to differentiate into tumour antigen-presenting DCs. Without conventional antigen-loading, DCs derived from the minigene-modified hPSCs were ready to prime a tumour antigen-specific T cell response and further expand these specific T cells in restimulation processes. These expanded tumour antigen-specific T cells were potent effectors with central memory or effector memory phenotype. Thus, we demonstrated that immunocompetent tumour antigen-loaded DCs can be directly generated from antigenically modified hPSCs. Using such strategy, we can completely eliminate the conventional antigen-loading step and significantly simplify the production of DC vaccine from hPSCs.
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/180314
ISSN: 20452322
DOI: 10.1038/srep15262
Rights: Attribution 4.0 International
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