Kreitman Robert J
Clinical Immunotherapy Section, Laboratory of Molecular Biology, Centers for Cancer Research, National Cancer Institute, National Institutes of Health, 9000 Rockville Pike, Building 37, Room 5124b, Bethesda, MD 20892-4255, USA.
Expert Opin Biol Ther. 2004 Jul;4(7):1115-28. doi: 10.1517/14712598.4.7.1115.
Recombinant immunotoxins are fusion proteins which contain a ligand derived from the immune system fused to a toxin. The protein toxin is truncated to delete its binding domain, allowing selective ligand-directed binding. Growth factor fusion toxins are often considered immunotoxins. One of these molecules, containing the truncated diphtheria toxin and human IL-2 (Ontak), Ligand Pharmaceuticals), has been approved for the treatment of cutaneous T-cell lymphoma. Recombinant immunotoxins have also been produced containing the variable domains (Fv fragment) of monoclonal antibodies fused to toxins. These agents are relatively versatile with respect to the range of antigens possible. Several of these recombinant immunotoxins have showed clinical effectiveness in Phase I testing against haematological malignancies. One of these molecules, BL22, targets CD22 on hairy-cell leukaemia and has enabled patients to achieve complete remissions despite previous treatment and resistance to chemotherapy.
重组免疫毒素是一种融合蛋白,它包含一个源自免疫系统的配体与一种毒素融合而成。蛋白质毒素经过截短以删除其结合结构域,从而实现选择性的配体导向结合。生长因子融合毒素通常被视为免疫毒素。其中一种分子,包含截短的白喉毒素和人白细胞介素-2(Ontak, Ligand制药公司),已被批准用于治疗皮肤T细胞淋巴瘤。还制备了含有与毒素融合的单克隆抗体可变结构域(Fv片段)的重组免疫毒素。就可能的抗原范围而言,这些制剂相对通用。其中几种重组免疫毒素在针对血液系统恶性肿瘤的I期试验中显示出临床疗效。其中一种分子BL22靶向毛细胞白血病上的CD22,使患者尽管先前接受过治疗且对化疗耐药仍能实现完全缓解。