Highly Efficient Elimination of Colorectal Tumor-Initiating Cells by an EpCAM/CD3-Bispecific Antibody Engaging Human T Cells

被引:80
作者
Herrmann, Ines [1 ]
Baeuerle, Patrick A. [1 ,2 ]
Friedrich, Matthias [1 ]
Murr, Alexander [1 ]
Filusch, Susanne [1 ]
Ruettinger, Dominik [1 ]
Majdoub, Mariam W. [3 ]
Sharma, Sherven [4 ,5 ]
Kufer, Peter [1 ]
Raum, Tobias [1 ]
Muenz, Markus [1 ]
机构
[1] Micromet AG, Munich, Germany
[2] Micromet Inc, Bethesda, MD USA
[3] Celprogen Inc, San Pedro, CA USA
[4] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90024 USA
[5] Greater Los Angeles Healthcare Syst, Mol Gene Med Lab, Los Angeles, CA USA
关键词
CANCER STEM-CELLS; EP-CAM; IMMUNOTHERAPEUTIC TARGET; BISPECIFIC ANTIBODIES; THERAPEUTIC WINDOW; ANTITUMOR-ACTIVITY; ADHESION MOLECULE; OVARIAN-CANCER; BREAST-CANCER; BITE ANTIBODY;
D O I
10.1371/journal.pone.0013474
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
With their resistance to genotoxic and anti-proliferative drugs and potential to grow tumors and metastases from very few cells, cancer stem or tumor-initiating cells (TICs) are a severe limitation for the treatment of cancer by conventional therapies. Here, we explored whether human T cells that are redirected via an EpCAM/CD3-bispecific antibody called MT110 can lyse colorectal TICs and prevent tumor growth from TICs. MT110 recognizes EpCAM, a cell adhesion molecule expressed on TICs from diverse human carcinoma, which was recently shown to promote tumor growth through engagement of elements of the wnt pathway. MT110 was highly potent in mediating complete redirected lysis of KRAS-, PI3 kinase- and BRAF-mutated colorectal TICs, as demonstrated in a soft agar assay. In immunodeficient mice, MT110 prevented growth of tumors from a 5,000-fold excess of a minimally tumorigenic TIC dose. T cells engaged by MT110 may provide a potent therapeutic means to eradicate TICs and bulk tumor cells derived thereof.
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页数:10
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