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鞘内注射单链免疫毒素LMB-7 [B3(Fv)-PE38]可治愈大鼠模型中的癌性脑膜炎。

Intrathecal administration of single-chain immunotoxin, LMB-7 [B3(Fv)-PE38], produces cures of carcinomatous meningitis in a rat model.

作者信息

Pastan I H, Archer G E, McLendon R E, Friedman H S, Fuchs H E, Wang Q C, Pai L H, Herndon J, Bigner D D

机构信息

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-4255, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2765-9. doi: 10.1073/pnas.92.7.2765.

Abstract

LMB-7 [B3(Fv)-PE38] is a single-chain immunotoxin constructed from the murine monoclonal antibody B3 and a truncated from of Pseudomonas exotoxin PE38. Antibody B3 recognizes a carbohydrate epitope found on solid tumors that frequently invade the intrathecal space and cause neoplastic meningitis. We tested the therapeutic value of intrathecally administered LMB-7 by using a model of human neoplastic meningitis in athymic rats. This model is representative of a clinical situation in that antibody B3 cross-reacts with a number of normal tissues that can be used to monitor potential systemic toxicity. Treatment was begun 3 days after A431 tumor implantation. Without treatment, the animals median survival was 10 days. Intrathecal administration of 10 micrograms of LMB-7 in 40 microliters on days 3, 5, and 7 produced 4 of 10 and 8 of 10 long-term survivors (> 170 days) in two experiments. Of the long-term survivors, 2 of 4 and 7 of 8 survivors had no microscopic evidence of tumor and were considered histologic cures. Lack of significant toxicity in the effective dose range and specificity make LMB-7 an excellent candidate for intrathecal treatment of neoplastic meningitis in humans.

摘要

LMB - 7 [B3(Fv)-PE38]是一种单链免疫毒素,由鼠单克隆抗体B3和铜绿假单胞菌外毒素PE38的截短形式构建而成。抗体B3识别实体瘤上发现的一种碳水化合物表位,这些实体瘤常侵犯鞘内间隙并导致肿瘤性脑膜炎。我们通过使用无胸腺大鼠的人肿瘤性脑膜炎模型来测试鞘内注射LMB - 7的治疗价值。该模型代表了一种临床情况,即抗体B3与许多可用于监测潜在全身毒性的正常组织发生交叉反应。在植入A431肿瘤3天后开始治疗。未经治疗,动物的中位生存期为10天。在两个实验中,分别于第3、5和7天鞘内注射40微升含10微克LMB - 7的溶液,产生了10只中的4只和10只中的8只长期存活者(> 170天)。在长期存活者中,4只中的2只和8只中的7只存活者没有肿瘤的微观证据,被认为是组织学治愈。在有效剂量范围内缺乏明显毒性以及具有特异性,使得LMB - 7成为鞘内治疗人类肿瘤性脑膜炎的极佳候选药物。

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