← 返回

抗体工程在从 MOv19 单抗衍生分子开发中的作用:抗叶酸受体 α 生物/治疗工具 40 年

英文原题:Role of antibody engineering in generation of derivatives starting from MOv19 MAb: 40 years of biological/therapeutic tools against folate receptor alfa.

查看英文原题

Role of antibody engineering in generation of derivatives starting from MOv19 MAb: 40 years of biological/therapeutic tools against folate receptor alfa.

PubMed 2022/10/27(内容时间) Antib Ther Q2 · IF 4.8(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

20世纪80年代,我们开发并表征了多种靶向人肿瘤相关抗原的小鼠单克隆抗体(mAb)。本文简要综述抗叶酸受体(FR)单克隆抗体MOv19衍生物的开发,重点介绍过去40年抗体工程技术的进展。FR位于增殖上皮细胞的管腔侧表面,血液循环中的抗体难以接触;但其在多种癌细胞整个表面过表达,这提示抗FR单克隆抗体可能用于实体瘤诊断和/或治疗。目前有两种MOv19衍生物进入临床试验:一种为经过嵌合化和表面重塑的抗体药物偶联物(SORAYA试验,2022年);另一种是由小鼠单链可变片段构成的第二代嵌合抗原受体(CAR)T细胞疗法(Ia期,2021年)。MOv19及其衍生物表明,充分表征的抗肿瘤小鼠单克隆抗体与抗体工程技术相结合,可开发出有价值的治疗工具。

展开英文摘要原文

In the 1980s, we developed and characterized numerous murine monoclonal antibodies (MAbs) directed against human tumor-associated antigens. This mini review is focused on the generation of derivatives of an anti-folate receptor (FR ) MAbs, named MOv19, exploiting the antibody-engineering progresses in the last 40 years. The FR location on the luminal surface of proliferating epithelial cells, inaccessible to circulation, versus its over-expression in the entire surface of numerous carcinomas suggested a role for anti-FR MAbs in the diagnosis and/or treatment of solid tumors.

Presently, two MOv19 derivatives are in clinical trials: a chimeric resurfaced version in an antibody-drug conjugate format (SORAYA trial, 2022) and the murine scFv in a second generation chimeric antigen receptor, CAR-T (Phase Ia, 2021). MOv19 and its derivatives could be considered a relevant example that well-characterized anti-tumor murine Mabs and antibody engineering could be combined to generate useful therapeutic tools.

论文信息

作者
Frigerio B、Montermini M、Silvana C、Figini M
单位
Biomarkers Unit, Department of Applied Research and Technical Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan 20133, Italy.Italy
文献类型
综述
期刊
Antibody therapeutics2022 Oct
原文标识
PubMed 36518225 · DOI 10.1093/abt/tbac026