San Diego Biomedical Research Institute, 10865 Road to the Cure, Suite 100, San Diego, CA 92121, USA.
Brain. 2021 Mar 3;144(2):402-410. doi: 10.1093/brain/awaa427.
Over the past 50 years, intense research effort has taught us a great deal about multiple sclerosis. We know that it is the most common neurological disease affecting the young-middle aged, that it affects two to three times more females than males, and that it is characterized as an autoimmune disease, in which autoreactive T lymphocytes cross the blood-brain barrier, resulting in demyelinating lesions. But despite all the knowledge gained, a key question still remains; what is the initial event that triggers the inflammatory demyelinating process? While most research effort to date has focused on the immune system, more recently, another potential candidate has emerged: hypoxia. Specifically, a growing number of studies have described the presence of hypoxia (both 'virtual' and real) at an early stage of demyelinating lesions, and several groups, including our own, have begun to investigate how manipulation of inspired oxygen levels impacts disease progression. In this review we summarize the findings of these hypoxia studies, and in particular, address three main questions: (i) is the hypoxia found in demyelinating lesions 'virtual' or real; (ii) what causes this hypoxia; and (iii) how does manipulation of inspired oxygen impact disease progression?
在过去的 50 年里,大量的研究工作让我们对多发性硬化症有了很多了解。我们知道,多发性硬化症是最常见的影响中青年人群的神经退行性疾病,女性的发病率是男性的两到三倍,其特征是一种自身免疫性疾病,其中自身反应性 T 淋巴细胞穿过血脑屏障,导致脱髓鞘病变。但尽管我们已经获得了很多知识,一个关键问题仍然存在:引发炎症性脱髓鞘过程的初始事件是什么?尽管迄今为止大多数研究都集中在免疫系统上,但最近另一个潜在的候选因素出现了:缺氧。具体来说,越来越多的研究描述了脱髓鞘病变早期存在缺氧(包括“虚拟”和真实),包括我们自己在内的几个研究小组已经开始研究如何操纵吸入氧气水平来影响疾病进展。在这篇综述中,我们总结了这些缺氧研究的发现,特别是回答了三个主要问题:(i)脱髓鞘病变中发现的缺氧是“虚拟”还是真实的;(ii)是什么导致了这种缺氧;以及(iii)操纵吸入氧气如何影响疾病进展?