抗iglon5疾病患者鞘内B细胞和浆细胞增加:一个病例系列

IF 7.5
Christine Strippel, Anna Heidbreder, Andreas Schulte-Mecklenbeck, Lisanne Korn, Tobias Warnecke, Nico Melzer, Heinz Wiendl, Matthias Pawlowski, Catharina C Gross, Stjepana Kovac
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引用次数: 8

摘要

背景和目的:尽管检测到自身抗体,抗iglon5疾病历来被认为是一种tau相关的神经退行性疾病,治疗选择有限,对患者有害。观察到越来越多的病例提示潜在的炎症机制,早期发现为治疗干预提供了宝贵的机会。我们旨在通过研究抗iglon5患者的脑脊液进一步证实这一观点。方法:我们从数据库中确定了11例抗iglon5患者,并将20例进行性核上性麻痹(PSP)(作为一种非炎症性病变)患者和22例功能性神经障碍患者的临床、MRI和CSF结果进行了比较。结果:与psp对照组和功能性神经疾病对照组相比,抗iglon5患者在常规脑脊液分析中显示炎症改变,b淋巴细胞频率增加,浆细胞存在。鞘内浆细胞患者对利妥昔单抗有临床反应。讨论:我们的研究结果表明炎症机制的重要性,特别是在早期和急性抗iglon5病例中,这可能支持在这些病例中使用免疫抑制治疗。该研究的主要局限性是病例数量少,因为这种疾病很罕见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series.

Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series.

Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series.

Increased Intrathecal B and Plasma Cells in Patients With Anti-IgLON5 Disease: A Case Series.

Background and objectives: Despite detection of autoantibodies, anti-IgLON5 disease was historically considered a tau-associated neurodegenerative disease, with limited treatment options and detrimental consequences for the patients. Observations in increasing case numbers hint toward underlying inflammatory mechanisms that, early detection provided, open a valuable window of opportunity for therapeutic intervention. We aimed to further substantiate this view by studying the CSF of patients with anti-IgLON5.

Methods: We identified 11 patients with anti-IgLON5 from our database and compared clinical, MRI, and CSF findings with a cohort of 20 patients with progressive supranuclear palsy (PSP) (as a noninflammatory tauopathy) and 22 patients with functional neurologic disorder.

Results: Patients with anti-IgLON5 show inflammatory changes in routine CSF analysis, an increase in B-lymphocyte frequency, and the presence of plasma cells in comparison to the PSP-control group and functional neurologic disease controls. Patients with intrathecal plasma cells showed a clinical response to rituximab.

Discussion: Our findings indicate the importance of inflammatory mechanisms, in particular in early and acute anti-IgLON5 cases, which may support the use of immune-suppressive treatments in these cases. The main limitation of the study is the small number of cases due to the rarity of the disease.

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