Binding Affinity, Specificity and Comparative Biodistribution of the Parental Murine Monoclonal Antibody MX35 (Anti-NaPi2b) and Its Humanized Version Rebmab200

نویسندگان

  • Sture Lindegren
  • Luciana N. S. Andrade
  • Tom Bäck
  • Camila Maria L. Machado
  • Bruno Brasil Horta
  • Carlos Buchpiguel
  • Ana Maria Moro
  • Oswaldo Keith Okamoto
  • Lars Jacobsson
  • Elin Cederkrantz
  • Kohshin Washiyama
  • Emma Aneheim
  • Stig Palm
  • Holger Jensen
  • Maria Carolina B. Tuma
  • Roger Chammas
  • Ragnar Hultborn
  • Per Albertsson
چکیده

The aim of this preclinical study was to evaluate the characteristics of the monoclonal antibody Rebmab200, which is a humanized version of the ovarian-specific murine antibody MX35. This investigation contributes to the foundation for future clinical α-radioimmunotherapy of minimal residual ovarian cancer with 211At-Rebmab200. Here, the biodistribution of 211At-Rebmab200 was evaluated, as was the utility of 99mTc-Rebmab200 for bioimaging. Rebmab200 was directly compared with its murine counterpart MX35 in terms of its in-vitro capacity for binding the immobilized NaPi2B epitope and live cells; we also assessed its biodistribution in nude mice carrying subcutaneous OVCAR-3 tumors. Tumor antigen and cell binding were similar between Rebmab200 and murine MX35, as was biodistribution, including normal tissue uptake and in-vivo tumor binding. We also demonstrated that 99mTc-Rebmab200 can be used for single-photon emission computed tomography of subcutaneous ovarian carcinomas in tumor-bearing mice. Taken together, our data support the further development of Rebmab200 for radioimmunotherapy and diagnostics.

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عنوان ژورنال:

دوره 10  شماره 

صفحات  -

تاریخ انتشار 2015