Case Reports:
BCMab1-Ra, a novel immunotoxin that BCMab1 antibody coupled to Ricin A chain, can eliminate bladder tumor
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Abstract
Chong Li1,5,*, Ruping Yan2,*, Zhao Yang3,*, Haifeng Wang2, Ruiyun Zhang4, Haige Chen4, Jiansong Wang2
1Core Facility for Protein Research, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China
2Department of Urology, The Second Affliated Hospital of Kunming Medical University, Kunming 650101, China
3CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China
4Department of Urology, Renji Hospital Affiliated to Shanghai Jiaotong University, School of Medicine, Shanghai 200127, China
5Beijing Jianlan Institute of Medicine, Beijing 100190, China
*These authors contributed equally to this work
Correspondence to:
Chong Li, email: [email protected]
Jiansong Wang, email: [email protected]
Haige Chen, email: [email protected]
Keywords: BCMab1, BCMab1-Ra, bladder cancer, aberrantly glycosylated integrin a3b1
Received: October 06, 2016 Accepted: November 08, 2016 Published: November 22, 2016
ABSTRACT
Bladder cancer is one of the most common malignancies. However, there is no ideal therapy to cure bladder cancer so far, especially invasive carcinoma. Here, we developed a new antibody-based drug BCMab1-Ra, which was generated by conjugation of BCMab1 (a new monoclonal antibody that specifically recognized the aberrantly glycosylated Integrin a3b1 in bladder cancer) with the ricin A chain (Ra). A patient with multiple bladder cancer received intravescical administration of BCMab1-Ra treatment as a volunteer. After 30 weeks of treatment, no tumor was observed by cystoscope examination. We did not observe any local or systemic side effects. Human anti-mouse antibody (HAMA) was not detectable in the circulation. Results follow-up showed no tumor had been found in every half year review in 3 years.
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