Abstract | OBJECTIVES: METHODS: We generated CSC-loaded dendritic cells (DCs) to sensitize autologous peripheral blood T, B lymphocytes to react with CSCs using human HNSCC samples in vitro. RESULTS: From peripheral blood collected from patients with HNSCC, we obtained PBMCs. DCs generated from the PBMC and pulsed with the lysate of ALDH(high) cells isolated from cultured HNSCC cells (CSC-DC) could sensitize autologous T, B lymphocytes in vitro, which was evident by cytokine production, CTL activity, and antibody secretion of these primed T, B cells in response to ALDH(high) CSCs. In contrast, DCs pulsed with lysate of ALDH(low) cells (ALDH(low)-DC) resulted in limited sensitization/priming of autologous T, B lymphocytes to produce IFNγ, GM-CSF; lyse CSCs, and secrete IgM and IgG in response to ALDH(high) CSCs. These results demonstrated significant differences in the antigenicity/immunogenicity between ALDH(high) CSCs vs. ALDH(low) cells isolated from the tumor specimen of patients with HNSCC, which indicates the existence of unique CSC antigens in the ALDH(high) population. CONCLUSION: It is feasible to generate DCs from the PBMCs and isolate ALDH(high) CSCs from cultured tumor cells of the patients with HNSCC to prepare CSC-DC vaccines that can induce anti- HNSCC CSC cellular and humoral immunity, indicating its potential clinical application to treat patients with HNSCC.
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Authors | Mark E P Prince, Li Zhou, Jeffrey S Moyer, Huimin Tao, Lin Lu, John Owen, Martin Etigen, Fang Zheng, Alfred E Chang, Jianchuan Xia, Gregory Wolf, Max S Wicha, Shiang Huang, Xiubao Ren, Qiao Li |
Journal | Oral oncology
(Oral Oncol)
Vol. 59
Pg. 30-42
(08 2016)
ISSN: 1879-0593 [Electronic] England |
PMID | 27424180
(Publication Type: Journal Article)
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Copyright | Copyright © 2016 Elsevier Ltd. All rights reserved. |
Chemical References |
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Topics |
- Aldehyde Dehydrogenase
(metabolism)
- B-Lymphocytes
(cytology)
- Carcinoma, Squamous Cell
(immunology)
- Cell Line, Tumor
- Dendritic Cells
(cytology)
- Head and Neck Neoplasms
(immunology)
- Humans
- Leukocytes, Mononuclear
- Neoplastic Stem Cells
(immunology)
- T-Lymphocytes
(cytology)
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