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借助百日咳菌苗在小鼠中诱发实验性变应性脑脊髓炎(EAE)

Elicitation of experimental allergic encephalomyelitis (EAE) in mice with the aid of pertussigen.

作者信息

Munoz J J, Bernard C C, Mackay I R

出版信息

Cell Immunol. 1984 Jan;83(1):92-100. doi: 10.1016/0008-8749(84)90228-4.

Abstract

Pertussigen, one of the biologically active proteins from Bordetella pertussis, was found highly active as an adjuvant to promote the induction of experimental allergic encephalomyelitis (EAE) in (SJL X BALB/c)F1 mice that had received at the same time an injection of mouse spinal cord (MSC) homogenized in complete Freund's adjuvant containing 4 mg of Mycobacterium tuberculosis H37RA per milliliter (CFA-H37). In this system 2 mg of MSC induced EAE, but a dose of 4 mg was more effective. As little as 250 ng of pertussigen facilitated induction of EAE, and 400 ng uniformly did so. Pertussigen was most effective when given iv from 1 day before to 5 days after administration of MSC homogenized in CFA-H37, when a uniform and severe disease was induced 11-13 days after immunization. Pertussigen given as late as 20 days after MSC-CFA-H37 still precipitated a mild form of EAE which appeared 8-12 days after the injection of pertussigen. When pertussigen was given 5 days after immunization, a chronic, nonfatal type of EAE was induced, and this persisted for the entire 74 days of observation. Histologic findings in the brain and spinal cord 15 days after sensitization in mice which received pertussigen and developed EAE showed perivascular infiltrates consisting mainly of mononuclear cells.

摘要

百日咳杆菌素是百日咳博德特氏菌的生物活性蛋白之一,在(SJL×BALB/c)F1小鼠中,它作为佐剂具有很高的活性,能促进实验性变态反应性脑脊髓炎(EAE)的诱导,这些小鼠同时接受了在每毫升含4毫克结核分枝杆菌H37RA的完全弗氏佐剂(CFA-H37)中匀浆的小鼠脊髓(MSC)注射。在这个系统中,2毫克的MSC可诱导EAE,但4毫克的剂量更有效。低至250纳克的百日咳杆菌素就能促进EAE的诱导,400纳克则总能诱导成功。当在注射CFA-H37中匀浆的MSC前1天至后5天静脉注射百日咳杆菌素时效果最佳,此时在免疫后11 - 13天会诱导出一致且严重的疾病。在MSC-CFA-H37注射后20天给予百日咳杆菌素仍会引发轻度的EAE,在注射百日咳杆菌素后8 - 12天出现。当在免疫后5天给予百日咳杆菌素时,会诱导出一种慢性、非致死性的EAE,并且在整个74天的观察期内持续存在。在接受百日咳杆菌素并发生EAE的小鼠致敏15天后,脑和脊髓的组织学检查发现血管周围浸润主要由单核细胞组成。

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