International Journal of Cancer · 2012 · 14 citations · 40 references
MedicineImmunologyOncologyCancer ImmunologyMetastasisTumor ImmunologyCancer ImmunosurveillanceCancer ImmunotherapyCancer VaccinesImmunotherapy For Solid TumorsTumor AntigensTumor-associated AntigensAntibodiesCancer AntigensCell LysisMonoclonal Antibodies In OncologyTherapeutic Cancer ImmunizationTumor Antibody ResponsesTumor Antigen VaccinesTumor-associated Antigen Vaccines
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.
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Carcinoembryonic antigen, a human tumor marker, functions as an intercellular adhesion molecule
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Tumor measurement in the nude mouse
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