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[单克隆抗体治疗脑膜胶质瘤病的免疫疗法实验研究]

[Experimental study on immunotherapy of meningeal gliomatosis with monoclonal antibody].

作者信息

Yamashita Y, Takahashi H, Nakazawa S

机构信息

Department of Neurosurgery, Nippon Medical School, Tokyo, Japan.

出版信息

No To Shinkei. 1993 Jan;45(1):63-70.

PMID:8476656
Abstract

Recently extension of malignant glioma to the spinal cord (meningeal gliomatosis: MG) has been described with increasing frequency as the advancement of the therapy for brain tumor. However, the study for clinicopathological features of MG has not been established and its therapy has still been difficult. We tried to produce experimental models of MG using nude mice and study experimental immunotherapy with human monoclonal antibody (CLN-IgG MoAb). U87-SC1 human glioma cells (5 x 10(5) in 20 microliters) were inoculated transcutaneously into the cisterna magna of BALB/c nu/nu mice using a 27-gage needle. Daily weights, neurological findings and survival time were examined. MRI scan was performed after neurological deterioration and histological examination was also performed after death. CLN-IgG MoAb was used for treatment and 15 nude mice which were inoculated with tumor cells into the cisterna magna (Day 0) were divided into three groups of 5 mice each. Group A was control group which received saline into the cisterna magna, Group B and C received 50 micrograms of CLN-IgG into the cisterna magna on Day 2 or Day 7 following inoculation of tumor cells. Efficacy of experimental immunotherapy was statistically evaluated by the difference of median survival time (MST) among three groups. All of the nude mice lost weight within 4 or 5 days after inoculation of tumor cells and developed paraplegia or tetraplegia with incontinence and died. MRI of the nude mice which showed neurological deteriorations revealed ventricular dilatation, infiltration of tumor cells to the spinal cord and spread of tumor cells into the subarachnoid space.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

近年来,随着脑肿瘤治疗方法的进步,恶性胶质瘤向脊髓扩展(脑膜胶质瘤病:MG)的报道越来越频繁。然而,关于MG临床病理特征的研究尚未确立,其治疗仍然困难。我们试图用裸鼠建立MG实验模型,并用人单克隆抗体(CLN-IgG单克隆抗体)研究实验性免疫治疗。使用27号针头将20微升含5×10⁵个U87-SC1人胶质瘤细胞经皮接种到BALB/c nu/nu小鼠的枕大池中。检查每日体重、神经学表现和存活时间。在神经功能恶化后进行MRI扫描,死亡后也进行组织学检查。CLN-IgG单克隆抗体用于治疗,将15只在枕大池接种肿瘤细胞的裸鼠(第0天)分为三组,每组5只。A组为对照组,向枕大池注射生理盐水,B组和C组在接种肿瘤细胞后的第2天或第7天向枕大池注射50微克CLN-IgG。通过三组中位生存时间(MST)的差异对实验性免疫治疗的疗效进行统计学评估。所有裸鼠在接种肿瘤细胞后4或5天内体重减轻,出现截瘫或四肢瘫伴大小便失禁并死亡。MRI显示神经功能恶化的裸鼠表现为脑室扩张、肿瘤细胞浸润脊髓以及肿瘤细胞扩散至蛛网膜下腔。(摘要截断于250字)

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