El Ayoubi Nabil K, Khoury Samia J
American University of Beirut and Medical Center, Nehme and Therese Tohme Multiple Sclerosis Center, Riad El Solh, Beirut, 1107 2020, Lebanon.
Neurotherapeutics. 2017 Jan;14(1):135-147. doi: 10.1007/s13311-016-0486-7.
Multiple sclerosis (MS) is an autoimmune demyelinating disorder of the central nervous system. Only a few biomarkers are available in MS clinical practice, such as cerebrospinal fluid oligoclonal bands and immunoglobulin index, serum anti-aquaporin 4 antibodies, and serum anti-John Cunningham virus antibodies. Thus, there is a significant unmet need for biomarkers to assess prognosis, response to therapy, or potential treatment complications. Here we describe emerging biomarkers that are in development, focusing on those from peripheral blood. There are several limitations in the process of discovery and validation of a good biomarker, such as the pathophysiological complexity of MS and the technical difficulties in globally standardizing methods for sampling, processing, and conserving biological specimens. In spite of these limitations, ongoing international collaborations allow the exploration of many interesting molecules and markers to validate diagnostic, prognostic, and therapeutic-response biomarkers.
多发性硬化症(MS)是一种中枢神经系统的自身免疫性脱髓鞘疾病。在MS临床实践中,可用的生物标志物较少,如脑脊液寡克隆带和免疫球蛋白指数、血清抗水通道蛋白4抗体以及血清抗约翰·坎宁安病毒抗体。因此,对于评估预后、治疗反应或潜在治疗并发症的生物标志物存在重大未满足需求。在此,我们描述正在开发的新兴生物标志物,重点关注外周血中的生物标志物。在发现和验证良好生物标志物的过程中存在若干限制,例如MS的病理生理复杂性以及在全球范围内标准化生物样本采样、处理和保存方法的技术困难。尽管存在这些限制,但正在进行的国际合作使得能够探索许多有趣的分子和标志物,以验证诊断、预后和治疗反应生物标志物。