Beck Alain, Haeuw Jean-François, Wurch Thierry, Goetsch Liliane, Bailly Christian, Corvaïa Nathalie
Department of Physico-Chemistry, Centre d'Immunologie Pierre Fabre (CIPF), St Julien-en-Genevois 74164, France.
Discov Med. 2010 Oct;10(53):329-39.
Monoclonal antibodies (mAbs) and derivatives are currently the fastest growing class of therapeutic molecules. More than 30 G-type immunoglobulins (IgG) and related agents have been approved over the past 25 years mainly for cancers and inflammatory diseases. In oncology, mAbs are often combined with cytotoxic drugs to enhance their therapeutic efficacy. Alternatively, small anti-neoplastic molecules can be chemically conjugated to mAbs, used both as carriers (increased half-life) and as targeting agents (selectivity). Potential benefits of antibody-drug conjugates (ADCs), strategies, and development challenges are discussed in this review. Several examples of ADCs are presented with emphasis on three major molecules currently in late clinical development as well as next generation thio-mAbs conjugates with improved therapeutic index.
单克隆抗体(mAb)及其衍生物是目前增长最快的一类治疗性分子。在过去25年中,已有30多种G型免疫球蛋白(IgG)及相关药物获批,主要用于治疗癌症和炎症性疾病。在肿瘤学领域,单克隆抗体常与细胞毒性药物联合使用以提高治疗效果。此外,小分子抗肿瘤药物可与单克隆抗体进行化学偶联,既作为载体(延长半衰期)又作为靶向剂(提高选择性)。本综述讨论了抗体药物偶联物(ADC)的潜在益处、策略及开发挑战。文中给出了几个ADC的例子,重点介绍了目前处于临床后期开发阶段的三种主要分子,以及具有更高治疗指数的下一代硫醇化单克隆抗体偶联物。