Abstract

<p><span lang="EN-US">Breast cancers have high recurrence rates with current treatment remaining palliative. Especially breast cancer–initiating cells have been recently identified in breast carcinoma as CD44<sup>+</sup>/CD24<sup>-/low</sup> cells, which exclusively retain tumorigenic activity and display stem cell–like properties. Immunotherapies harness the body’s own immune system to target cancers and could overcome the limitations of conventional treatments. One active immunotherapy strategy uses dendritic cell (DC)-based vaccination to initiate T-cell-mediated antitumor immunity. However, whether using human BSC antigens may improve the antitumor effect of DC vaccination against BSC is indistinct. In this study, we isolated and evaluated BSCs derived from breast cancer patients, and explored the suitability of BSCs as sources of antigens for DC vaccination again human BSCs, with the aim of achieving BSC targeting and enhanced antitumor immunity. We found that BSCs express high levels of stem cell-associated molecules, CD44<sup>+</sup>/CD24<sup>-</sup> and CD133<sup>+</sup>, but adherent cells express CD44<sup>+</sup>/CD24<sup>+</sup> and low CD133<sup>+</sup>. </span><span lang="EN-US">The enriched mammospheric cells have a stronger tumorigenic capacity than adherent cells in vivo </span><span lang="EN-US"><a href="http://dict.cn/Tumorigenesis"><span>tumorigenesis</span></a></span><span lang="EN-US">.</span><span lang="EN-US"> DC vaccination using BSC lysates elicited specific T-cell responses against BSCs. DC vaccination </span><span lang="EN-US">stimulated Th1 response and induced significant IFN-</span><span lang="EN-US">γ </span><span lang="EN-US">production</span><span lang="EN-US"> which is positively correlated with the number of cytotoxic T lymphocytes (CTLs)</span><span lang="EN-US"> stimulated</span><span lang="EN-US">. Strikingly, using BSC breast cancer model, we demonstrate that vaccination with CTL </span><span lang="EN-US">stimulated</span><span lang="EN-US"> DCs pulsed with </span><span lang="EN-US">enriched </span><span lang="EN-US">mammospheric cells lysates, but not pulsed with adherent cells lysates, prolonged survival in animals bearing BSC breast cancer tumors. Therefore, these proof-of-concept results confirmed CD44<sup>+</sup>/CD24<sup>-</sup>/CD133<sup>+</sup> mammospheric cells have stem cells </span><span lang="EN-US"><a href="http://dict.cn/property"><span>property</span></a></span><span lang="EN-US"> and DC immunization with BSCs generates superior antitumor immunity which may accelerate development of BSC-specific immunotherapies and cancer vaccines.</span></p>

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