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Recent Advances on the Possible Neuroprotective Activities of Epstein-Barr Virus Oncogene BARF1 Protein in Chronic Inflammatory Disorders of Central Nervous System

机译:爱泼斯坦-巴尔病毒癌基因BARF1蛋白在中枢神经系统慢性炎性疾病中可能的神经保护活性的最新进展

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摘要

Multiple sclerosis and neurodegenerative diseases in which cells of the central nervous system (CNS) are lost or damaged are rapidly increasing in frequency, and there is neither effective treatment nor cure to impede or arrest their destructive course. The Epstein-Barr virus is a human gamma-herpesvirus that infects more than 90% of the human population worldwide and persisting for the lifetime of the host. It is associated with numerous epithelial cancers, principally undifferentiated nasopharyngeal carcinoma and gastric carcinoma. Individuals with a history of symptomatic primary EBV infection, called infectious mononucleosis, carry a moderately higher risk of developing multiple sclerosis (MS). It is not known how EBV infection potentially promotes autoimmunity and central nervous system (CNS) tissue damage in MS. Recently it has been found that EBV isolates from different geographic regions have highly conserved BARF1 epitopes. BARF1 protein has the neuroprotective and mitogenic activity, thus may be useful to combat and overcome neurodegenerative disease. BARF1 protein therapy can potentially be used to enhance the neuroprotective activities by combinational treatment with anti-inflammatory antagonists and neuroprotectors in neural disorders.
机译:中枢神经系统(CNS)细胞丢失或损坏的多发性硬化症和神经退行性疾病的频率迅速增加,并且既没有有效的治疗方法也没有治愈或阻止其破坏性进程的方法。爱泼斯坦-巴尔病毒是一种人类伽玛疱疹病毒,感染了全世界90%以上的人口,并在宿主的整个生命周期中持续存在。它与多种上皮癌有关,主要是未分化的鼻咽癌和胃癌。有症状的原发性EBV感染史的个体(称为传染性单核细胞增多症)携带多发性硬化症(MS)的风险较高。尚不清楚EBV感染如何潜在地促进MS中的自身免疫和中枢神经系统(CNS)组织损伤。最近发现,来自不同地理区域的EBV分离株具有高度保守的BARF1表位。 BARF1蛋白具有神经保护和促有丝分裂活性,因此可能可用于对抗和克服神经退行性疾病。通过与神经疾病中的抗炎拮抗剂和神经保护剂联合治疗,BARF1蛋白疗法可潜在地用于增强神经保护活性。

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