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球后视神经炎。无多发性硬化症患者对髓鞘碱性蛋白致敏的体外证据。

Retrobulbar neuritis. In vitro evidence of sensitization to myelin basic protein in patients without multiple sclerosis.

作者信息

Sheremata W, Younge B, Eylar E H

出版信息

Neurology. 1977 Jun;27(6):557-60. doi: 10.1212/wnl.27.6.557.

Abstract

Thirty-six normal subjects and 34 patients with retrobulbar neuritis were studied with use of the technique of macrophage migration inhibition factor assay and myelin basic protein as antigen. Serial studies were carried out when possible. Normal subjects gave a mean migration index of 100.9+/-9. Eleven patients with retrobulbar neuritis alone gave a mean migration index of 55+/-16 in the first 3 weeks of illness, 89+/-17.3 during the fourth to the twenty-fourth weeks, and 100.9+/-9.0 after the twenty-fourth week. Ten multiple sclerosis patients with retrobulbar neuritis gave values of 61+/-21 in the first 3 weeks of an attack and 92+/-22.8 during the fourth to the twenty-fourth weeks, and 12 other multiple sclerosis patients 24 weeks or longer after an attack gave a value of 101.9+/-12.6. In a mean follow-up period of 1.9 years, only two patients presenting with retrobulbar neuritis alone have had a diagnosis of multiple sclerosis established; three others have weakness and reflex change in one limb only; and four have minor psychiatric problems. One retrobulbar neuritis patient has a family history of multiple sclerosis, but has no neurologic abnormalities. Comparison of these studies in both groups shows no statistical differences and supports the concept that cell-mediated hypersensitization to central nervous system myelin basic protein, however initiated, is a factor in the pathogenesis of retrobulbar neuritis.

摘要

采用巨噬细胞移动抑制因子测定技术,以髓鞘碱性蛋白为抗原,对36名正常受试者和34名球后视神经炎患者进行了研究。可能的情况下进行了系列研究。正常受试者的平均移动指数为100.9±9。仅患有球后视神经炎的11名患者在发病的前3周平均移动指数为55±16,在第4至24周为89±17.3,在第24周后为100.9±9.0。10名患有球后视神经炎的多发性硬化症患者在发作的前3周的值为61±21,在第4至24周为92±22.8,另外12名发作后24周或更长时间的多发性硬化症患者的值为101.9±12.6。在平均1.9年的随访期内,仅患有球后视神经炎的患者中只有2例被诊断为多发性硬化症;另外3例仅一侧肢体有无力和反射改变;4例有轻微精神问题。1例球后视神经炎患者有家族性多发性硬化症病史,但无神经学异常。两组这些研究的比较显示无统计学差异,支持以下概念:无论如何引发,对中枢神经系统髓鞘碱性蛋白的细胞介导超敏反应是球后视神经炎发病机制中的一个因素。

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