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Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells

The inability to target cancer stem cells (CSC) may be a significant factor contributing to treatment failure. We have developed a strategy to target the CSC populations in melanoma and squamous cell carcinoma using CSC lysate-pulsed dendritic cells (DCs). The CSC-DC vaccine was administered in the...

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Autores principales: Lu, Lin, Tao, Huimin, Chang, Alfred E, Hu, Yangyang, Shu, Guoshun, Chen, Quanning, Egenti, Martin, Owen, John, Moyer, Jeffrey S, Prince, Mark EP, Huang, Shiang, Wicha, Max S, Xia, Jian-Chuan, Li, Qiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404925/
https://www.ncbi.nlm.nih.gov/pubmed/25949905
http://dx.doi.org/10.4161/2162402X.2014.990767
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author Lu, Lin
Tao, Huimin
Chang, Alfred E
Hu, Yangyang
Shu, Guoshun
Chen, Quanning
Egenti, Martin
Owen, John
Moyer, Jeffrey S
Prince, Mark EP
Huang, Shiang
Wicha, Max S
Xia, Jian-Chuan
Li, Qiao
author_facet Lu, Lin
Tao, Huimin
Chang, Alfred E
Hu, Yangyang
Shu, Guoshun
Chen, Quanning
Egenti, Martin
Owen, John
Moyer, Jeffrey S
Prince, Mark EP
Huang, Shiang
Wicha, Max S
Xia, Jian-Chuan
Li, Qiao
author_sort Lu, Lin
collection PubMed
description The inability to target cancer stem cells (CSC) may be a significant factor contributing to treatment failure. We have developed a strategy to target the CSC populations in melanoma and squamous cell carcinoma using CSC lysate-pulsed dendritic cells (DCs). The CSC-DC vaccine was administered in the adjuvant setting after localized radiation therapy of established tumors. Using mouse models we demonstrated that DCs pulsed with CSCs enriched by virtue of their expression of the CSC marker ALDH (termed CSC-DC) significantly inhibited tumor growth, reduced development of pulmonary metastases and prolonged survival. The effect was associated with downregulation of chemokine (C-C motif) receptors CCR7 and CCR10 in tumor cells and decreased expression of the chemokine (C-C motif) ligands CCL21, CCL27 and CCL28 in lung tissue. The CSC-DC vaccine significantly reduced ALDH(high) CSC frequency in primary tumors. Direct targeting of CSCs was demonstrated by the specific binding of IgG produced by ALDH(high) CSC-DC vaccine-primed B cells to ALDH(high) CSCs, resulting in lysis of these target CSCs in the presence of complement. These data suggest that the CSC-DC vaccine approach may be useful in the adjuvant setting where local and systemic relapse are high after conventional treatment of cancers.
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spelling pubmed-44049252016-01-09 Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells Lu, Lin Tao, Huimin Chang, Alfred E Hu, Yangyang Shu, Guoshun Chen, Quanning Egenti, Martin Owen, John Moyer, Jeffrey S Prince, Mark EP Huang, Shiang Wicha, Max S Xia, Jian-Chuan Li, Qiao Oncoimmunology Original Research The inability to target cancer stem cells (CSC) may be a significant factor contributing to treatment failure. We have developed a strategy to target the CSC populations in melanoma and squamous cell carcinoma using CSC lysate-pulsed dendritic cells (DCs). The CSC-DC vaccine was administered in the adjuvant setting after localized radiation therapy of established tumors. Using mouse models we demonstrated that DCs pulsed with CSCs enriched by virtue of their expression of the CSC marker ALDH (termed CSC-DC) significantly inhibited tumor growth, reduced development of pulmonary metastases and prolonged survival. The effect was associated with downregulation of chemokine (C-C motif) receptors CCR7 and CCR10 in tumor cells and decreased expression of the chemokine (C-C motif) ligands CCL21, CCL27 and CCL28 in lung tissue. The CSC-DC vaccine significantly reduced ALDH(high) CSC frequency in primary tumors. Direct targeting of CSCs was demonstrated by the specific binding of IgG produced by ALDH(high) CSC-DC vaccine-primed B cells to ALDH(high) CSCs, resulting in lysis of these target CSCs in the presence of complement. These data suggest that the CSC-DC vaccine approach may be useful in the adjuvant setting where local and systemic relapse are high after conventional treatment of cancers. Taylor & Francis 2015-01-09 /pmc/articles/PMC4404925/ /pubmed/25949905 http://dx.doi.org/10.4161/2162402X.2014.990767 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Original Research
Lu, Lin
Tao, Huimin
Chang, Alfred E
Hu, Yangyang
Shu, Guoshun
Chen, Quanning
Egenti, Martin
Owen, John
Moyer, Jeffrey S
Prince, Mark EP
Huang, Shiang
Wicha, Max S
Xia, Jian-Chuan
Li, Qiao
Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells
title Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells
title_full Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells
title_fullStr Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells
title_full_unstemmed Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells
title_short Cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells
title_sort cancer stem cell vaccine inhibits metastases of primary tumors and induces humoral immune responses against cancer stem cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404925/
https://www.ncbi.nlm.nih.gov/pubmed/25949905
http://dx.doi.org/10.4161/2162402X.2014.990767
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