1. Academic Validation
  2. Generation of a canine anti-canine CD20 antibody for canine lymphoma treatment

Generation of a canine anti-canine CD20 antibody for canine lymphoma treatment

  • Sci Rep. 2020 Jul 10;10(1):11476. doi: 10.1038/s41598-020-68470-9.
Takuya Mizuno 1 Yukinari Kato 2 3 Mika K Kaneko 2 Yusuke Sakai 4 Toshinori Shiga 5 Masahiro Kato 5 Toshihiro Tsukui 5 Hirofumi Takemoto 6 Akio Tokimasa 6 Kenji Baba 6 Yuki Nemoto 7 Osamu Sakai 7 Masaya Igase 7
Affiliations

Affiliations

  • 1 Laboratory of Molecular Diagnostics and Therapeutics, The United Graduate School of Veterinary Medicine, Yamaguchi University, 1677-1 Yoshida, Yamaguchi, Yamaguchi Prefecture, 753-8515, Japan. [email protected].
  • 2 Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.
  • 3 New Industry Creation Hatchery Center, Tohoku University, Miyagi, Japan.
  • 4 Laboratory of Veterinary Pathology, Joint Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi, Japan.
  • 5 Nippon Zenyaku Kogyo Co., Ltd., Koriyama, Fukushima, Japan.
  • 6 Laboratory of Veterinary Internal Medicine, Joint Faculty of Veterinary Medicine, Yamaguchi University, Yamaguchi, Japan.
  • 7 Laboratory of Molecular Diagnostics and Therapeutics, The United Graduate School of Veterinary Medicine, Yamaguchi University, 1677-1 Yoshida, Yamaguchi, Yamaguchi Prefecture, 753-8515, Japan.
Abstract

Lymphoma is the most common hematological Cancer in dogs. Canine diffuse large B cell lymphoma shows a relatively good response to treatment with multi-agent cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy; however, the 2-year survival rate is as low as 20%. For human B cell type lymphoma, the anti-CD20 chimeric antibody, rituximab, was developed two decades ago. The combination of rituximab and CHOP chemotherapy was highly successful in improving patient prognosis. However, no anti-canine CD20 antibody is available for the treatment of canine lymphoma. During this study, a rat anti-canine CD20 monoclonal antibody was established. We also generated a rat-canine chimeric antibody against canine CD20 designed for clinical application. This chimeric antibody (4E1-7-B) showed in vitro antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) against the canine B cell lymphoma cell line CLBL-1. Moreover, to obtain stronger ADCC activity, a defucosylated 4E1-7-B antibody (4E1-7-B_f) was also generated, and it showed tenfold stronger ADCC activity compared with 4E1-7-B. 4E1-7-B_f as well as 4E1-7-B suppressed the growth of CLBL-1 tumors in an immunodeficient xenotransplant mouse model. Finally, a single administration of 4E1-7-B_f induced considerable peripheral B cell depletion in healthy beagles. Thus, 4E1-7-B_f is a good antibody drug candidate for canine B cell type lymphoma.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-P99483
    99.08%, Anti-Canine CD20 Antibody