多发性硬化症免疫及免疫遗传学评价的临床意义。

P B Jozefczyk, R H Kelly, B S Rabin
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引用次数: 5

摘要

132例患者被分为临床定义的明确、可能和可能多发性硬化症(MS)、多发性硬化症脊髓变异型(SCV)和非多发性硬化症神经系统疾病组。HLA抗原A3和B7在明确的和可能的MS患者中出现的频率比神经系统对照组和健康成人高。脑脊液kappa/lambda比、IgG/总蛋白比或IgG升高在65%的确定、可能和SCV组中可见。HLA A3和B7抗原患者kappa/lambda比值升高的发生率高于预期,提示可能存在影响该CSF参数的免疫遗传控制机制。HLA抗原和脑脊液蛋白异常与发病年龄、进展或疾病残疾程度均无相关性,因此限制了其预后价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical significance of immunologic and immunogenetic evaluation in multiple sclerosis.

One hundred thirty-two patients were separated into clinically defined groups of definite, probable and possible multiple sclerosis (MS), the spinal cord variant of MS (SCV), and non MS neurologic disease. HLA antigens A3 and B7 occurred at increased frequencies in definite and probably MS patients when compared with neurologic controls and healthy adults. CSF elevations of either kappa/lambda ratio, IgG/total protein ratio, or IgG were seen in 65% of the definite, probable and SCV groups. Patients with HLA A3 and B7 antigens had a higher than predicted incidence of elevated kappa/lambda ratio, suggesting that there may be immunogenetic control mechanisms which influence this CSF parameter. Neither HLA antigens nor CSF protein abnormalities correlated with the age of onset, progression, or degree of disability of disease, thus limiting their prognostic usefulness.

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