Tumoral Immune Cell Exploitation in Colorectal Cancer Metastases Can Be Targeted Effectively by Anti-CCR5 Therapy in Cancer Patients

被引:419
作者
Halama, Niels [1 ,2 ,3 ]
Zoernig, Inka [1 ]
Berthel, Anna [1 ,2 ]
Kahlert, Christoph [4 ]
Klupp, Fee [4 ]
Suarez-Carmona, Meggy [1 ]
Suetterlin, Thomas [1 ,2 ]
Brand, Karsten [5 ]
Krauss, Juergen [1 ]
Lasitschka, Felix [5 ]
Lerchl, Tina [1 ,2 ]
Luckner-Minden, Claudia [1 ]
Ulrich, Alexis [4 ]
Koch, Moritz [6 ]
Weitz, Juergen [6 ]
Schneider, Martin [4 ]
Buechler, Markus W. [4 ]
Zitvogel, Laurence [7 ]
Herrmann, Thomas [8 ]
Benner, Axel [9 ]
Kunz, Christina [9 ]
Luecke, Stephan [9 ]
Springfeld, Christoph [1 ]
Grabe, Niels [1 ,2 ]
Falk, Christine S. [10 ]
Jaeger, Dirk [1 ,2 ]
机构
[1] Univ Heidelberg Hosp, Natl Ctr Tumor Dis, Dept Med Oncol, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, BIOQUANT, Natl Ctr Tumor Dis, Tissue Imaging & Anal Ctr, D-69120 Heidelberg, Germany
[3] Univ Heidelberg Hosp, Inst Immunol, D-69120 Heidelberg, Germany
[4] Univ Heidelberg Hosp, Dept Surg, D-69120 Heidelberg, Germany
[5] Univ Heidelberg Hosp, Inst Pathol, D-69120 Heidelberg, Germany
[6] Univ Hosp Dresden, Dept Surg, D-01307 Dresden, Germany
[7] IGR, INSERM U1015, F-94805 Villejuif, France
[8] Klinikum Idar Oberstein, Dept Internal Med 1, D-55743 Idar Oberstein, Germany
[9] German Canc Res Ctr, Div Biostat, D-69120 Heidelberg, Germany
[10] Hannover Med Sch, Integrated Res & Treatment Ctr Transplantat, Inst Transplant Immunol, D-30625 Hannover, Germany
关键词
MIGRATION INHIBITORY FACTOR; CHEMOKINE RECEPTOR CCR5; HEPATOCELLULAR-CARCINOMA; BREAST-CANCER; IMMUNOTHERAPY; INFLAMMATION; CHEMOTHERAPY; PROGRESSION; ANTAGONIST; EXPRESSION;
D O I
10.1016/j.ccell.2016.03.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 patientderived 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.
引用
收藏
页码:587 / 601
页数:15
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