抗体工程在生成从 MOv19 MAb 开始的衍生物中的作用:针对叶酸受体 alfa 的生物/治疗工具 40 年。

Q2 Medicine Antibody Therapeutics Pub Date : 2022-10-27 eCollection Date: 2022-10-01 DOI:10.1093/abt/tbac026
Barbara Frigerio, Matilde Montermini, Canevari Silvana, Mariangela Figini
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摘要

20 世纪 80 年代,我们开发并鉴定了许多针对人类肿瘤相关抗原的鼠类单克隆抗体(MAbs)。这篇微型综述的重点是利用过去 40 年中抗体工程的进步,研制出抗叶酸受体α(FRα)MAbs 的衍生物,并命名为 MOv19。FRα位于增殖上皮细胞的管腔表面,无法进入血液循环,而它在许多癌细胞的整个表面过度表达,这表明抗 FRα MAbs 可在实体瘤的诊断和/或治疗中发挥作用。目前,有两种 MOv19 衍生物正在进行临床试验:一种是抗体-药物共轭物形式的嵌合再表面化版本(SORAYA 试验,2022 年),另一种是第二代嵌合抗原受体 CAR-T 中的鼠 scFv(Ia 期,2021 年)。MOv19 及其衍生物可被视为一个相关范例,说明特征明确的抗肿瘤小鼠 Mabs 与抗体工程相结合,可以产生有用的治疗工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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 α (FRα) MAbs, named MOv19, exploiting the antibody-engineering progresses in the last 40 years. The FRα 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-FRα 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.

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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
期刊最新文献
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