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使用鼠-犬嵌合抗犬 Podoplanin 抗体的抗体药物偶联物在小鼠异种移植模型中发挥抗肿瘤活性。

Antibody-Drug Conjugates Using Mouse-Canine Chimeric Anti-Dog Podoplanin Antibody Exerts Antitumor Activity in a Mouse Xenograft Model.

机构信息

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.

New Industry Creation Hatchery Center, Tohoku University, Sendai, Japan.

出版信息

Monoclon Antib Immunodiagn Immunother. 2020 Apr;39(2):37-44. doi: 10.1089/mab.2020.0001. Epub 2020 Mar 17.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fae/7185362/6e3ec3bcbee0/mab.2020.0001_figure1.jpg

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