A focused immune response targeting the homotypic binding domain of the carcinoembryonic antigen blocks the establishment of tumor foci in vivo

被引:13
作者
Abdul-Wahid, Aws [2 ,3 ]
Huang, Eric H. -B. [2 ,3 ]
Lu, Huixin
Flanagan, Jean [4 ]
Mallick, Amirul Islam [2 ,3 ]
Gariepy, Jean [1 ,2 ,3 ]
机构
[1] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Med Biophys, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Dept Pharmaceut Sci, Toronto, ON M4N 3M5, Canada
[3] Sunnybrook Res Inst, Toronto, ON, Canada
[4] Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON M4X 1K9, Canada
关键词
cancer vaccine; metastasis; carcinoembryonic antigen; antibody-dependent cytotoxicity; COLORECTAL-CARCINOMA CELLS; BREAST-CANCER; T-CELLS; INTERCELLULAR-ADHESION; ANTITUMOR-ACTIVITY; IG SUPERFAMILY; GASTRIC-CANCER; CEA; VACCINES; IDENTIFICATION;
D O I
10.1002/ijc.27582
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Metastatic forms of cancers remain the main cause of death in cancer patients. In this study, we demonstrate that directing a sustained antibody response towards the homotypic binding function of CEA interferes with the implantation and development of tumor foci in CEA-expressing transgenic (CEA.Tg) mice. Specifically, vaccinating CEA.Tg mice with a recombinant, altered self-form of the CEA Ig V-like N domain led to the production of circulating IgG1 and IgG2a antibodies that inhibited CEA-mediated adhesion of murine carcinoma expressing CEA (MC38.CEA) and mediated antibody-dependent lysis of tumor cells. Moreover, vaccinated CEA.Tg mice were resistant to the development of tumor nodules in the lungs and the peritoneal cavity, suggesting that mounting a focused antibody response to the CEA N domain may represent a simple therapeutic strategy to control the establishment of metastatic foci in cancer patients.
引用
收藏
页码:2839 / 2851
页数:13
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