Characterization of anti-canine CD20 antibody 4E1-7-B_f and comparison with commercially available anti-human CD20 antibodies
This study characterizes the previously reported anti-canine CD20 antibody 4E1-7-B_f and compares this with commercially available anti-human CD20 antibodies, rituximab and an obinutuzumab biosimilar. While the obinutuzumab biosimilar exhibited binding to canine CD20 in a CD20-transduced cell line, canine B-cell lymphoma cell line (CLBL-1/luc), and canine CD21 + B cells from healthy dogs, functional assays revealed the superiority of 4E1-7-B_f in antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity activities over those of the obinutuzumab biosimilar. Epitope analysis suggested an extracellular region on canine CD20 targeted by 4E1-7-B_f. Furthermore, the lipid raft localization of CD20 in CLBL-1/luc cells by treatment with 4E1-7-B_f classified this antibody as a type II anti-CD20 antibody which works with strong ADCC activity, similar to the obinutuzumab biosimilar, unlike rituximab, a type I anti-CD20 antibody, whose main action is CDC activity. These findings underscore the potential clinical utility of 4E1-7-B_f, emphasizing the specificity, potency, and therapeutic promise in canine lymphoma treatment.
Authors
- Takuya Mizuno (ORCID: https://orcid.org/0000-0002-9580-7557)
- Masaya Igase (ORCID: https://orcid.org/0000-0002-3118-8507)
- Yukinari Kato (ORCID: https://orcid.org/0000-0001-5385-8201)
- Toshihiro Tsukui (ORCID: https://orcid.org/0000-0001-8830-5930)
Institutions
- Yamaguchi University (JP)
- Tohoku University (JP)
- Zenyaku Kogyo (Japan) (JP)
Publication Details
- Journal
- PLoS ONE
- Published
- 2025-06-27
- DOI
- https://doi.org/10.1371/journal.pone.0325526
- Citations
- 1
- Primary Topic
- Cell Adhesion Molecules Research
- Type
- article
- Field-Weighted Citation Impact
- 1.62
Funders
- Japan Agency for Medical Research and Development
- Nippon Zenyaku Kogyo