Jons D, Sundström P, Andersen O
Section of Clinical Neuroscience and Rehabilitation, Institution of Neuroscience and Physiology, the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Acta Neurol Scand. 2015 Feb;131(2):69-79. doi: 10.1111/ane.12294. Epub 2014 Sep 11.
We here review contemporary data on genetic and environmental risk factors, particularly Epstein-Barr virus infection, for multiple sclerosis. There is an important immunogenetic etiological factor for multiple sclerosis. However, a general assumption is that immune defense genes are activated by the environment, basically by infections. We contend that the relationship between infectious mononucleosis and multiple sclerosis cannot be completely explained by genetics and inverse causality. Epstein-Barr infection as indicated by positive serology is an obligatory precondition for multiple sclerosis, which is a stronger attribute than a risk factor only. Data on events in the early pathogenesis of multiple sclerosis are cumulating from bio-banks with presymptomatic specimens, but there is only little information from the critical age when Epstein-Barr infection including infectious mononucleosis is acquired, nor on the detailed immunological consequences of this infection in individuals with and without multiple sclerosis. We discuss how focused bio-banking may elaborate a rationale for the development of treatment or vaccination against Epstein-Barr virus infection. A cohort in which intervention against Epstein-Barr infections was performed should be the object of neurological follow-up.
我们在此回顾有关多发性硬化症的遗传和环境风险因素,特别是爱泼斯坦-巴尔病毒感染的当代数据。多发性硬化症存在一个重要的免疫遗传病因因素。然而,一个普遍的假设是免疫防御基因是由环境激活的,基本上是由感染激活的。我们认为传染性单核细胞增多症与多发性硬化症之间的关系不能完全用遗传学和反向因果关系来解释。血清学阳性所表明的爱泼斯坦-巴尔病毒感染是多发性硬化症的一个必要前提条件,这一属性比仅仅作为一个风险因素更强。来自拥有症状前标本的生物样本库的关于多发性硬化症早期发病机制事件的数据正在不断积累,但关于获得爱泼斯坦-巴尔病毒感染(包括传染性单核细胞增多症)的关键年龄的信息很少,也没有关于这种感染在患有和未患多发性硬化症个体中的详细免疫后果的信息。我们讨论了有针对性的生物样本库如何为开发针对爱泼斯坦-巴尔病毒感染的治疗方法或疫苗提供理论依据。对爱泼斯坦-巴尔病毒感染进行干预的队列应该是神经学随访的对象。