Preclinical studies with JAA-F11 anti-Thomsen-Friedenreich monoclonal antibody for human breast cancer

Author:

Ferguson Kimiko1,Yadav Arti1,Morey Susan1,Abdullah Julia1,Hrysenko Gabriel1,Eng Jing Ying1,Sajjad Munawwar1,Koury Stephen1,Rittenhouse-Olson Kate1234

Affiliation:

1. Department of Biotechnical & Clinical Laboratory Sciences, University of Buffalo, Buffalo, NY 14214, USA

2. Department of Social & Preventative Medicine, University of Buffalo, Buffalo, NY 14214, USA

3. Department of Microbiology & Immunology, University of Buffalo, Buffalo, NY 14214, USA

4. Robin Therapeutics, 97 Troy View Lane, Buffalo, NY 14221, USA

Abstract

ABSTRACT:  Aim: The Thomsen-Friedenreich antigen (TF-Ag) is a disaccharide hidden on normal cells, but selectively exposed on the surface of breast, colon, prostate and bladder cancer cells. JAA-F11, a highly specific monoclonal antibody to TF-Ag, reduces metastasis and prolongs survival in a mouse model. In addition,124I-JAA-F11 localizes 4T1 tumors in mice. These studies continue translation of JAA-F11 to human breast cancer. Materials & methods & results: Of the 41 human breast cancer cell lines tested, 78% were positive for reactivity with JAA-F11 by whole-cell enzyme immunoassay and positivity occurred unrelated to estrogen, progesterone or HER2 receptor status. JAA-F11 inhibited the growth rate of the human cancer cell lines tested. At 1 h, approximately 80% of JAA-F11 internalized in the three cell lines tested. 124I-JAA-F11 specifically imaged human triple-negative tumors in mice by microPET. Conclusion: The results highlight the potential that humanized JAA-F11 may have for immunotherapy and drug conjugate therapy in breast cancer patients.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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