Anti -MBP autoantibody changes as a predictor of response to treatment in MS patients

Gholinejad Khadijeh, R. Ali, S. Ali, N. Saeed, Kazerouni Faranak, Naser Moghadasi Abdorreza, Rahimi Forough, Boroumandnia Nasrin
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引用次数: 1

Abstract

Myelin basic protein (MBP) is one of the most important constituents of the CNS myelin sheaths. It is supposed that an autoimmune response directed against MBP is crucial in the demyelination process in patients with multiple sclerosis. Studies have proved that free anti-MBP level in CSF of MS patients is declined when the patient entered into clinical remission. Some researchers evaluate the changes in serum or CSF level of this antibody during immunomodulatory therapy; the results are different and the relation between the changes in this antibody and response to treatment is poorly investigated. The objective of this study was to assess the relation between the changes in serum level of anti-MBP and clinical remission in patients during treatment with fingolimod. 37 MS patients that were non responder to interferon and glatiramer acetate and were candidates to receive fingolimod were nominated for this study.  In this study, the serum level of anti-MBP was evaluated before and after 3 and 6 months of therapy and clinical remission was assessed by changes in Expanded Disability Status Scale (EDSS) scores. The result of this study showed that MS patients, after treatment with interferon, have lower serum anti-MBP level than healthy control group and this difference is statistically significant (p =0.03).  The present study demonstrated that the serum anti-MBP level in MS patient during 6 months of treatment with fingolimod significantly decreased (p<0.001). However, there was no significant difference in EDSS of MS patients during 6 months of treatment with fingolimod ( p < 0.001).
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抗mbp自身抗体变化作为MS患者治疗反应的预测因子
髓鞘碱性蛋白(Myelin basic protein, MBP)是中枢神经系统髓鞘中最重要的成分之一。据推测,针对MBP的自身免疫反应在多发性硬化症患者脱髓鞘过程中至关重要。研究证明,MS患者进入临床缓解期后,CSF中游离抗mbp水平下降。一些研究者评价免疫调节治疗期间血清或脑脊液中该抗体水平的变化;结果是不同的,这种抗体的变化与治疗反应之间的关系研究得很少。本研究的目的是评估芬戈莫德治疗期间患者血清抗mbp水平变化与临床缓解之间的关系。37例对干扰素和醋酸格拉替默无反应的MS患者被提名接受芬戈莫德治疗。在这项研究中,在治疗前和治疗后3个月和6个月评估血清抗mbp水平,并通过扩展残疾状态量表(EDSS)评分的变化评估临床缓解。本研究结果显示,MS患者经干扰素治疗后血清抗mbp水平低于健康对照组,差异有统计学意义(p =0.03)。本研究表明,在芬戈莫德治疗6个月期间,MS患者血清抗mbp水平显著降低(p<0.001)。然而,在6个月的芬戈莫德治疗期间,MS患者的EDSS无显著差异(p < 0.001)。
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