癌症研究
单克隆抗体
癌症治疗
抗体
抗体疗法
医学
生物
癌症
癌细胞
免疫学
内科学
作者
Carola H. Ries,Michael A. Cannarile,Sabine Hoves,Jörg Benz,Katharina Wartha,Valeria Runza,Flora Rey-Giraud,Leon P. Pradel,Friedrich Feuerhake,Irina Klaman,Tobin Jones,Ute Jucknischke,Stefan Scheiblich,Klaus Kaluza,Ingo H. Gorr,Antje‐Christine Walz,K. Abiraj,Philippe Cassier,Antonio Sica,Carlos Gomez-Roca
出处
期刊:Cancer Cell
[Cell Press]
日期:2014-06-01
卷期号:25 (6): 846-859
被引量:1206
标识
DOI:10.1016/j.ccr.2014.05.016
摘要
Macrophage infiltration has been identified as an independent poor prognostic factor in several cancer types. The major survival factor for these macrophages is macrophage colony-stimulating factor 1 (CSF-1). We generated a monoclonal antibody (RG7155) that inhibits CSF-1 receptor (CSF-1R) activation. In vitro RG7155 treatment results in cell death of CSF-1-differentiated macrophages. In animal models, CSF-1R inhibition strongly reduces F4/80+ tumor-associated macrophages accompanied by an increase of the CD8+/CD4+ T cell ratio. Administration of RG7155 to patients led to striking reductions of CSF-1R+CD163+ macrophages in tumor tissues, which translated into clinical objective responses in diffuse-type giant cell tumor (Dt-GCT) patients.
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