Lanz Tobias V, Robinson William H, Ho Peggy P, Steinman Lawrence
Stanford University Stanford CA USA.
Clin Transl Immunology. 2023 Feb 16;12(2):e1438. doi: 10.1002/cti2.1438. eCollection 2023.
Here, we offer a roadmap for what might be studied next in understanding how EBV triggers MS. We focus on two areas: The first area concerns the underlying how clonal antibody in the CSF emanates in widespread molecular mimicry to key antigens in the nervous system including GlialCAM, a protein associated with chloride channels. A second and equally high priority in the roadmap concerns various that are related to blocking the mechanisms whereby EBV triggers MS. Therapies deserving of attention include clinical trials with antivirals and the development of 'inverse' vaccines based on nucleic acid technologies to control or to eradicate the consequences of EBV infection. High enthusiasm is given to continuation of ongoing clinical trials of cellular adoptive therapy to attack EBV-infected cells. Clinical trials of vaccines to EBV are another area deserving attention. These suggested topics involving research on mechanism, and the design, implementation and performance of well-designed trials are not intended to be an exhaustive list. We have splendid tools available to our community of medical scientists to tackle how EBV triggers MS and then to perhaps change the world with new therapies to potentially eradicate MS, as we have done with nearly complete success for poliomyelitis.
在此,我们提供了一份路线图,说明在理解EB病毒如何引发多发性硬化症(MS)方面接下来可能开展的研究。我们关注两个领域:第一个领域涉及脑脊液中的克隆抗体如何通过广泛的分子模拟作用于神经系统中的关键抗原,包括与氯离子通道相关的蛋白质胶质细胞粘附分子(GlialCAM)。路线图中的第二个同样高度优先的领域涉及与阻断EB病毒引发MS的机制相关的各种研究。值得关注的疗法包括抗病毒药物的临床试验,以及基于核酸技术开发“反向”疫苗以控制或消除EB病毒感染的后果。人们对继续进行细胞过继性疗法的临床试验以攻击被EB病毒感染的细胞充满热情。针对EB病毒的疫苗临床试验是另一个值得关注的领域。这些涉及机制研究以及精心设计试验的设计、实施和执行的建议主题并非详尽无遗的清单。我们医学科学家群体拥有出色的工具来解决EB病毒如何引发MS的问题,然后或许能用新疗法改变世界,有可能根除MS,就像我们在小儿麻痹症方面几乎取得完全成功那样。