| Literature DB >> 27070705 |
Niels Halama1, Inka Zoernig2, Anna Berthel3, Christoph Kahlert4, Fee Klupp5, Meggy Suarez-Carmona2, Thomas Suetterlin3, Karsten Brand6, Juergen Krauss2, Felix Lasitschka6, Tina Lerchl3, Claudia Luckner-Minden2, Alexis Ulrich5, Moritz Koch7, Juergen Weitz7, Martin Schneider5, Markus W Buechler5, Laurence Zitvogel8, Thomas Herrmann9, Axel Benner10, Christina Kunz10, Stephan Luecke10, Christoph Springfeld2, Niels Grabe3, Christine S Falk11, Dirk Jaeger3.
Abstract
The immune response influences the clinical course of colorectal cancer (CRC). Analyzing the invasive margin of human CRC liver metastases, we identified a mechanism of immune cell exploitation by tumor cells. While two distinct subsets of myeloid cells induce an influx of T cells into the invasive margin via CXCL9/CXCL10, CCL5 is produced by these T cells and stimulates pro-tumoral effects via CCR5. CCR5 blockade in patient-derived functional in vitro organotypic culture models showed a macrophage repolarization with anti-tumoral effects. These anti-tumoral effects were then confirmed in a phase I trial with a CCR5 antagonist in patients with liver metastases of advanced refractory CRC. Mitigation of tumor-promoting inflammation within the tumor tissue and objective tumor responses in CRC were observed.Entities:
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Year: 2016 PMID: 27070705 DOI: 10.1016/j.ccell.2016.03.005
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743