| Literature DB >> 25977333 |
Cristina Ghirelli1, Fabien Reyal2, Marine Jeanmougin1, Raphaël Zollinger1, Philémon Sirven1, Paula Michea1, Christophe Caux3, Nathalie Bendriss-Vermare3, Marie-Hélène Donnadieu1, Martial Caly4, Virginie Fourchotte5, Anne Vincent-Salomon4, Brigitte Sigal-Zafrani4, Xavier Sastre-Garau4, Vassili Soumelis6.
Abstract
Reciprocal interactions between tumor cells and their microenvironment vitally impact tumor progression. In this study, we show that GM-CSF produced by primary breast tumor cells induced the activation of plasmacytoid predendritic cells (pDC), a cell type critical to anti-viral immunity. pDC that expressed the GM-CSF receptor were increased in breast tumors compared with noninvolved adjacent breast tissue. Tumor-activated pDC acquired naïve CD4(+) T-cell stimulatory capacity and promoted a regulatory Th2 response. Finally, the concomitant increase of GM-CSF and pDC was significantly associated with relatively more aggressive breast cancer subtypes. Our results characterize the first tumor-derived factor that can activate pDC to promote a regulatory Th2 response, with implications for therapeutic targeting of a tumor-immune axis of growing recognition in its significance to cancer. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 25977333 DOI: 10.1158/0008-5472.CAN-14-2386
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701