Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
EMD Serono Research and Development Institute, Inc., Billerica, MA, USA.
Brain. 2021 Jun 22;144(5):1396-1408. doi: 10.1093/brain/awab045.
Leptomeningeal inflammation in multiple sclerosis is associated with worse clinical outcomes and greater cortical pathology. Despite progress in identifying this process in multiple sclerosis patients using post-contrast fluid-attenuated inversion recovery imaging, early trials attempting to target meningeal inflammation have been unsuccessful. There is a lack of appropriate model systems to screen potential therapeutic agents targeting meningeal inflammation. We utilized ultra-high field (11.7 T) MRI to perform post-contrast imaging in SJL/J mice with experimental autoimmune encephalomyelitis induced via immunization with proteolipid protein peptide (PLP139-151) and complete Freund's adjuvant. Imaging was performed in both a cross-sectional and longitudinal fashion at time points ranging from 2 to 14 weeks post-immunization. Following imaging, we euthanized animals and collected tissue for pathological evaluation, which revealed dense cellular infiltrates corresponding to areas of contrast enhancement involving the leptomeninges. These areas of meningeal inflammation contained B cells (B220+), T cells (CD3+) and myeloid cells (Mac2+). We also noted features consistent with tertiary lymphoid tissue within these areas, namely the presence of peripheral node addressin-positive structures, C-X-C motif chemokine ligand-13 (CXCL13)-producing cells and FDC-M1+ follicular dendritic cells. In the cortex adjacent to areas of meningeal inflammation we identified astrocytosis, microgliosis, demyelination and evidence of axonal stress/damage. Since areas of meningeal contrast enhancement persisted over several weeks in longitudinal experiments, we utilized this model to test the effects of a therapeutic intervention on established meningeal inflammation. We randomized mice with evidence of meningeal contrast enhancement on MRI scans performed at 6 weeks post-immunization, to treatment with either vehicle or evobrutinib [a Bruton tyrosine kinase (BTK) inhibitor] for a period of 4 weeks. These mice underwent serial imaging; we examined the effect of treatment on the areas of meningeal contrast enhancement and noted a significant reduction in the evobrutinib group compared to vehicle (30% reduction versus 5% increase; P = 0.003). We used ultra-high field MRI to identify areas of meningeal inflammation and to track them over time in SJL/J mice with experimental autoimmune encephalomyelitis, and then used this model to identify BTK inhibition as a novel therapeutic approach to target meningeal inflammation. The results of this study provide support for future studies in multiple sclerosis patients with imaging evidence of meningeal inflammation.
多发性硬化症中的软脑膜炎症与更差的临床结局和更大的皮质病变有关。尽管使用对比后液体衰减反转恢复成像在多发性硬化症患者中识别这种过程已经取得了进展,但早期试图靶向脑膜炎症的试验都没有成功。缺乏适当的模型系统来筛选针对脑膜炎症的潜在治疗药物。我们利用超高场(11.7 T)MRI 在通过用蛋白脂质蛋白肽(PLP139-151)和完全弗氏佐剂免疫诱导实验性自身免疫性脑脊髓炎的 SJL/J 小鼠中进行对比后成像。在免疫后 2 至 14 周的时间点以横断面和纵向方式进行成像。成像后,我们对动物进行安乐死并收集组织进行病理评估,结果显示脑膜对比增强区域存在密集的细胞浸润,涉及软脑膜。这些脑膜炎症区域含有 B 细胞(B220+)、T 细胞(CD3+)和髓样细胞(Mac2+)。我们还注意到这些区域内存在与三级淋巴组织一致的特征,即存在外周节点地址素阳性结构、C-X-C 基序趋化因子配体 13(CXCL13)产生细胞和 FDC-M1+滤泡树突状细胞。在与脑膜炎症区域相邻的皮质中,我们发现了星形胶质细胞增生、小胶质细胞增生、脱髓鞘和轴突应激/损伤的证据。由于脑膜对比增强区域在纵向实验中持续数周,我们利用该模型测试了对已建立的脑膜炎症的治疗干预的效果。我们对在免疫后 6 周进行的 MRI 扫描中显示脑膜对比增强的小鼠进行随机分组,分别接受载体或 evobrutinib(Bruton 酪氨酸激酶(BTK)抑制剂)治疗 4 周。这些小鼠进行了连续成像;我们检查了治疗对脑膜对比增强区域的影响,并注意到 evobrutinib 组与载体组相比有显著减少(30%减少与 5%增加;P=0.003)。我们利用超高场 MRI 来识别实验性自身免疫性脑脊髓炎 SJL/J 小鼠的脑膜炎症区域,并随时间跟踪它们,然后利用该模型来识别 BTK 抑制作为靶向脑膜炎症的新治疗方法。这项研究的结果为多发性硬化症患者的脑膜炎症影像学证据提供了支持未来的研究。