Mizuno Takuya, Kato Yukinari, Tsukui Toshihiro, Igase Masaya
Laboratory of Molecular Diagnostics and Therapeutics, Joint Graduate School of Veterinary Medicine, Yamaguchi University, Yamaguchi, Japan.
Division of Translational Research for One Medicine, Research Institute for Cell Design Medical Science, Yamaguchi University, Yamaguchi, Japan.
PLoS One. 2025 Jun 27;20(6):e0325526. doi: 10.1371/journal.pone.0325526. eCollection 2025.
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.
本研究对先前报道的抗犬CD20抗体4E1-7-B_f进行了表征,并将其与市售的抗人CD20抗体利妥昔单抗和一种奥妥珠单抗生物类似药进行比较。虽然该奥妥珠单抗生物类似药在转导CD20的细胞系、犬B细胞淋巴瘤细胞系(CLBL-1/luc)以及健康犬的犬CD21 + B细胞中表现出与犬CD20的结合,但功能分析显示4E1-7-B_f在抗体依赖性细胞毒性和补体依赖性细胞毒性活性方面优于该奥妥珠单抗生物类似药。表位分析表明4E1-7-B_f靶向犬CD2上的一个细胞外区域。此外,通过用4E1-7-B_f处理CLBL-1/luc细胞中CD20的脂筏定位,将该抗体归类为II型抗CD20抗体,其作用类似于奥妥珠单抗生物类似药,具有很强的抗体依赖性细胞介导的细胞毒性(ADCC)活性,这与I型抗CD20抗体利妥昔单抗不同,后者的主要作用是补体依赖性细胞毒性(CDC)活性。这些发现强调了4E1-7-B_f潜在的临床应用价值,突出了其在犬淋巴瘤治疗中的特异性、效力和治疗前景。