Abstract
JAA-F11 antibody (Ab) is a monoclonal Ab that is specific for the Thomsen-Friedenreich antigen, Galβ1-3GalNAcα (TF-Ag). TF-Ag, discovered in the late 1920s, is a tumor-associated carbohydrate Ag of many clinically widespread carcinomas. In a mouse model, JAA-F11 Ab significantly extended median survival time of animals with metastatic 4T1 breast tumors and caused > 50% inhibition of lung metastasis. 124Iodine labeled JAA-F11 Ab in in vivo micro positron emission tomography showed tumor specificity in a mouse breast tumor model, with no preferential uptake by any other organ. Human cancer cell adhesion to vascular endothelium was also blocked by JAA-F11. Structural specificity of the Ab was shown with glycan array analysis and indicated that this Ab, unlike many other Abs to TF-Ag, will not bind to a related glycolipid on natural killer cells, kidney or spleen. Patients with higher levels of naturally occurring anti-TF-Ag Ab appear to have a better prognosis, indicating that passive transfer of JAA-F11 or active immunization, resulting in production of anti-TF-Ag Ab, would clinically be beneficial for the patient.
| Original language | English |
|---|---|
| Pages (from-to) | 923-928 |
| Number of pages | 6 |
| Journal | Expert Opinion on Biological Therapy |
| Volume | 7 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 2007 |
Keywords
- Breast cancer
- Carbohydrate antigens
- Carcinomas
- Imaging
- Immunotherapy
- JAA-F11
- Metastasis
- Positron emission tomography
- Prostate cancer
- Radiolocalization
- TF-Ag
- Thomsen-friedenreich antigen
- Tumor antigens
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