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Antigenically Modified Human Pluripotent Stem Cells Generate Antigen-Presenting Dendritic Cells.
- Source :
-
Scientific reports [Sci Rep] 2015 Oct 16; Vol. 5, pp. 15262. Date of Electronic Publication: 2015 Oct 16. - Publication Year :
- 2015
-
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.
- Subjects :
- Antigens, Neoplasm genetics
Antigens, Neoplasm immunology
CD8-Positive T-Lymphocytes cytology
CD8-Positive T-Lymphocytes immunology
CD8-Positive T-Lymphocytes metabolism
Cancer Vaccines immunology
Cell Line
Dendritic Cells cytology
Dendritic Cells immunology
Epitopes genetics
Epitopes immunology
Epitopes metabolism
Genes, Reporter
Genetic Vectors genetics
Genetic Vectors metabolism
Humans
Immunocompetence
MART-1 Antigen genetics
MART-1 Antigen immunology
MART-1 Antigen metabolism
Neoplasms therapy
Pluripotent Stem Cells cytology
Pluripotent Stem Cells metabolism
Response Elements genetics
Antigens, Neoplasm metabolism
Dendritic Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 5
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 26471005
- Full Text :
- https://doi.org/10.1038/srep15262