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一种抗体-细胞毒素偶联物 BIIB015 是一种针对 Cripto 阳性肿瘤的新型靶向治疗药物。

An antibody-cytotoxic conjugate, BIIB015, is a new targeted therapy for Cripto positive tumours.

机构信息

Biogen Idec, Inc, Discovery Oncology, 14 Cambridge Center, Cambridge, MA 02142, USA.

出版信息

Eur J Cancer. 2011 Jul;47(11):1736-46. doi: 10.1016/j.ejca.2011.02.023. Epub 2011 Mar 31.

Abstract

BIIB015 is an immunoconjugate created for the treatment of solid tumours and is currently in Phase I of clinical evaluation. BIIB015 consists of a humanised monoclonal antibody against the Cripto protein carrying a payload, via a hindered disulphide linker, of the maytansinoid derivative, DM4. Cripto is a GPI-linked protein required for signal transduction of the TGF-beta ligand, Nodal. Cripto has been previously described as an oncogene and fits the classic pattern of an embryonic gene that is re-expressed in a transformed tumour cell. Cripto expression is highly prevalent on a number of solid tumours, including greater than 75% of breast, lung, and colorectal tumours. Our report documents for the first time that targeting the cell surface Cripto protein with an anti-Cripto antibody-cytotoxic conjugate is an effective means of inhibiting or regressing growth of Cripto positive tumours. BIIB015 which utilises a 'cleavable' linker containing a disulphide bond exhibits superior activity when compared to huB3F6 mAb conjugates with different linker systems, including one with a 'non-cleavable' linker. BIIB015 displays specificity for Cripto in both in vitro and in vivo experiments. In human xenograft models originating from lung (Calu-6), colon (CT-3), testicular (NCCIT) and breast (MDA-MB-231) tumour samples, BIIB015 shows robust activity with results ranging from >50% tumour inhibition to complete tumour regression. The efficacy seen in the MDA-MB-231 model, a triple negative (-HER2, -ER, and -PR) tumour, is particularly exciting since there is currently no approved therapy for this indication. In addition, BIIB015 can be combined with standard of care chemotherapeutics for enhanced efficacy.

摘要

BIIB015 是一种用于治疗实体瘤的免疫偶联物,目前处于临床评估的 I 期。BIIB015 由一种针对 Cripto 蛋白的人源化单克隆抗体组成,该抗体通过受阻的二硫键连接体携带一种美登素衍生物 DM4 的有效载荷。Cripto 是一种 GPI 连接的蛋白,是 TGF-β配体 Nodal 信号转导所必需的。Cripto 先前被描述为一种癌基因,符合经典的胚胎基因模式,即在转化的肿瘤细胞中重新表达。Cripto 在许多实体瘤中高度表达,包括超过 75%的乳腺癌、肺癌和结直肠癌。我们的报告首次证明,用抗 Cripto 抗体-细胞毒素偶联物靶向细胞表面 Cripto 蛋白是抑制或消退 Cripto 阳性肿瘤生长的有效方法。BIIB015 利用含有二硫键的“可裂解”连接体,与具有不同连接体系统的 huB3F6 mAb 缀合物(包括具有“不可裂解”连接体的缀合物)相比,具有更高的活性。BIIB015 在体外和体内实验中均显示出对 Cripto 的特异性。在源自肺(Calu-6)、结肠(CT-3)、睾丸(NCCIT)和乳腺(MDA-MB-231)肿瘤样本的人异种移植模型中,BIIB015 显示出强大的活性,结果范围从>50%的肿瘤抑制到完全肿瘤消退。在 MDA-MB-231 模型中观察到的疗效特别令人兴奋,因为目前没有针对这种适应症的批准疗法。此外,BIIB015 可以与标准护理化疗药物联合使用以提高疗效。

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