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柔脑膜瘤的免疫毒素治疗

Immunotoxin therapy of leptomeningeal neoplasia.

作者信息

Walbridge S, Rybak S M

机构信息

Surgical Neurology Branch, National Institute of Neurological Diseases and Stroke, National Institutes of Health, Bethesda, MD 20892.

出版信息

J Neurooncol. 1994;20(1):59-65. doi: 10.1007/BF01057962.

Abstract

Malignant tumors of the central nervous system can result from metastatic dissemination of a variety of cancers. Percutaneous intracisternal injection of an anti-idiotype monoclonal antibody (M6) ricin immunotoxin was shown to be moderately effective in prolonging the survival of tumor bearing animals supporting the use of immunotoxins for the treatment of central nervous system neoplasia (Zovickian J and Youle R.J. J. Neurosurg 68: 767, 1988). This report describes a method that significantly improves the survival of immunotoxin treated Strain 2 guinea pigs in a syngeneic animal model of leptomeningeal neoplasia. Strain 2 guinea pigs, implanted with subarachnoid catheters, received three courses of treatment with an (M6)-intract ricin immunotoxin following intracisternal inoculation of L2C leukemia tumor cells. Animals were treated with three to four micrograms of immunotoxin in three divided doses. This was found to be less toxic and more effective than single bolus administration of immunotoxin. These results demonstrate that a permanent indwelling catheter in this animal model facilitates multiple dose delivery of immunotoxin therapy allowing the assessment of various treatment schedules and the achievement of enhanced therapeutic effect. Furthermore, these results support the continued evaluation of immunotoxins for the treatment of central nervous system neoplasia.

摘要

中枢神经系统恶性肿瘤可能由多种癌症的转移扩散引起。经皮脑池内注射抗独特型单克隆抗体(M6)蓖麻毒素免疫毒素,在延长荷瘤动物生存期方面显示出一定效果,支持将免疫毒素用于治疗中枢神经系统肿瘤(佐维基安J和尤尔RJ。《神经外科杂志》68:767,1988)。本报告描述了一种方法,该方法在软脑膜肿瘤形成的同基因动物模型中显著提高了免疫毒素治疗的2系豚鼠的生存期。给植入蛛网膜下腔导管的2系豚鼠在脑池内接种L2C白血病肿瘤细胞后,给予三个疗程的(M6)-内毒素蓖麻毒素免疫毒素治疗。动物接受三至四微克免疫毒素,分三次给药。结果发现,这比单次推注免疫毒素毒性更小且更有效。这些结果表明,在该动物模型中使用永久性留置导管有助于多次给药免疫毒素治疗,从而能够评估各种治疗方案并实现增强的治疗效果。此外,这些结果支持继续评估免疫毒素用于治疗中枢神经系统肿瘤。

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