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JAA-F11: Extending the life of mice with breast cancer

Research output: Contribution to journalReview articlepeer-review

13 Scopus citations

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 languageEnglish
Pages (from-to)923-928
Number of pages6
JournalExpert Opinion on Biological Therapy
Volume7
Issue number7
DOIs
StatePublished - 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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