Johnson V G, Wrobel C, Wilson D, Zovickian J, Greenfield L, Oldfield E H, Youle R
Surgical Neurology Branch, National Institute of Neurological Communicative Diseases and Stroke, Bethesda, Maryland.
J Neurosurg. 1989 Feb;70(2):240-8. doi: 10.3171/jns.1989.70.2.0240.
A novel antibody-toxin conjugate has been developed for use in cancer therapy. This report demonstrates that this new reagent selectively kills glioblastoma- and medulloblastoma-derived cell lines, medulloblastoma cells in primary culture, and cell lines derived from tumors commonly metastatic to the cerebrospinal fluid (CSF). Efficient killing of human tumor cells occurred at concentrations between 3.9 X 10(-13) M and 1.1 X 10(-10) M, whereas guinea pigs and rhesus monkeys tolerated intrathecal levels of 2 X 10(-9) M. Cerebrospinal fluid from normal humans and from brain-tumor patients does not inhibit the in vitro efficacy of this reagent. The wide therapeutic window, extreme potency, and general applicability of this antibody-toxin conjugate against CSF-borne primary or metastatic tumors warrants clinical trials.
一种新型抗体-毒素偶联物已被开发用于癌症治疗。本报告表明,这种新试剂能选择性杀死源自胶质母细胞瘤和髓母细胞瘤的细胞系、原代培养的髓母细胞瘤细胞,以及源自通常转移至脑脊液(CSF)的肿瘤的细胞系。在浓度介于3.9×10⁻¹³ M和1.1×10⁻¹⁰ M之间时,可有效杀死人类肿瘤细胞,而豚鼠和恒河猴可耐受鞘内注射2×10⁻⁹ M的水平。正常人和脑肿瘤患者的脑脊液均不抑制该试剂的体外疗效。这种抗体-毒素偶联物针对脑脊液传播的原发性或转移性肿瘤具有较宽的治疗窗口、极高的效力和广泛的适用性,值得进行临床试验。