Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
New Industry Creation Hatchery Center, Tohoku University, Sendai, Japan.
Monoclon Antib Immunodiagn Immunother. 2020 Apr;39(2):37-44. doi: 10.1089/mab.2020.0001. Epub 2020 Mar 17.
Antibody-drug conjugates (ADCs), which consist of a monoclonal antibody (mAb), a linker, and a payload, can deliver a drug to cancer tissues. We previously produced an anti-dog podoplanin (dPDPN) mAb, PMab-38, which reacts with dPDPN-expressing canine melanomas and squamous cell carcinomas (SCCs), but not with dPDPN-expressing canine type I alveolar cells or lymphatic endothelial cells, indicating that PMab-38 possesses cancer specificity. In this study, we developed an ADC, P38B-DM1, using the mouse-canine chimeric anti-dPDPN antibody, P38B as the antibody, a peptide linker, and emtansine as the payload using the chemical conjugation by affinity peptide (CCAP) method. We investigated its cytotoxicity against dPDPN-overexpressed Chinese hamster ovary (CHO/dPDPN) cells and its antitumor activity using a mouse xenograft model of CHO/dPDPN cells. P38B-DM1 showed cytotoxicity to CHO/dPDPN cells in a dose-dependent manner . Furthermore, P38B-DM1 exhibited higher antitumor activity than P38B in the mouse xenograft model. These results suggest that P38B-DM1, developed using the CCAP method, is useful for antibody therapy against dPDPN-expressing canine SCCs and melanomas.
抗体药物偶联物(ADCs)由单克隆抗体(mAb)、连接子和有效载荷组成,可将药物递送至癌症组织。我们之前生产了一种抗犬 Podoplanin(dPDPN)的 mAb,PMab-38,它与表达 dPDPN 的犬黑色素瘤和鳞状细胞癌(SCC)反应,但不与表达 dPDPN 的犬Ⅰ型肺泡细胞或淋巴内皮细胞反应,表明 PMab-38 具有癌症特异性。在这项研究中,我们使用小鼠-犬嵌合抗 dPDPN 抗体 P38B 作为抗体、肽连接子和埃坦西胺作为有效载荷,开发了一种 ADC,P38B-DM1,使用化学偶联亲和肽(CCAP)方法。我们研究了它对过表达 dPDPN 的中国仓鼠卵巢(CHO/dPDPN)细胞的细胞毒性及其在 CHO/dPDPN 细胞的小鼠异种移植模型中的抗肿瘤活性。P38B-DM1 对 CHO/dPDPN 细胞表现出剂量依赖性的细胞毒性。此外,P38B-DM1 在小鼠异种移植模型中表现出比 P38B 更高的抗肿瘤活性。这些结果表明,使用 CCAP 方法开发的 P38B-DM1 可用于针对表达 dPDPN 的犬 SCC 和黑色素瘤的抗体治疗。