黑色素瘤特异性免疫毒素ME20-LysPE40的抗肿瘤活性。

Therapeutic immunology Pub Date : 1995-06-01
E A Wolff, I Hellström, D F Chace, K E Hellström, C B Siegall
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引用次数: 0

摘要

通过将具有黑色素瘤选择性的内化抗体ME20与假单胞菌外毒素a的结合缺陷形式LysPE40连接,制备了一种免疫毒素偶联物。ME20- lyspe40与存在于黑色素瘤细胞(ME20- m)上的105,000 Da细胞表面抗原结合,在未经修饰的ME20的两倍范围内,对两种人类黑色素瘤细胞系H3606和MALME-3M具有细胞毒性,EC50值分别为100和200 pM。免疫毒素治疗在H3606黑色素瘤细胞皮下植入小鼠后1天开始,在> 50%的小鼠中阻止肿瘤异种移植物的生长。相比之下,如果在小鼠体内传代的H3606肿瘤片段植入5天后给予免疫毒素,则仅观察到对肿瘤生长的适度抑制。本研究表明,内源性单克隆抗体ME20 IgG可用于将毒素靶向显示ME20- m抗原的黑色素瘤细胞。
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Antitumour activity of a melanoma-specific immunotoxin, ME20-LysPE40.

An immunotoxin conjugate has been prepared by linking an internalizing antibody with melanoma selectivity, ME20, with a binding-defective form of Pseudomonas exotoxin A, LysPE40. ME20-LysPE40 binds to a 105,000 Da cell-surface antigen present on melanoma cells (ME20-M) within twofold of unmodified ME20 and was cytotoxic to two human melanoma cell lines, H3606 and MALME-3M, with EC50 values of 100 and 200 pM, respectively. Immunotoxin treatment, initiated 1 day following subcutaneous implantation of H3606 melanoma cells into mice, prevented outgrowth of tumour xenografts in > 50% of the mice. In contrast, only a modest inhibition in tumour growth was observed if the immunotoxin was administered 5 days after implantation of in vivo passaged H3606 tumour fragments in mice. This study shows that the internalizing monoclonal antibody ME20 IgG can be used for targeting a toxin toward melanoma cells displaying the ME20-M antigen.

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