运动神经元疾病患者开始使用反义寡核苷酸疗法后脑脊液中的巨噬细胞包涵体。

Q2 Medicine
Maximilian Vidovic, Mario Menschikowski, Maren Freigang, Hanna Sophie Lapp, René Günther
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引用次数: 0

摘要

5q相关性脊髓性肌萎缩症(SMA)和肌萎缩侧索硬化症(ALS)是两种不同的神经系统疾病,会导致低级运动神经元变性。反义寡核苷酸(ASO)nusinersen 和 tofersen 分别是治疗这两种疾病的新型药物。在 ASO 治疗的背景下,脑脊液(CSF)的细胞学特征和成分最近引起了人们的特别关注。本报告介绍了两例 SMA 和 ALS 患者脑脊液细胞学检查结果的病例系列,这两例患者在开始接受纽西奈森和托福森治疗后发现了类似的不明巨噬细胞包涵体。然而,在两种不同的 ASO 治疗过程中出现这些 "嗜磷细胞 "的意义尚不明确。虽然这两种疗法的耐受性都很好,但考虑到这些疗法的长期性,这一现象值得关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macrophage inclusions in cerebrospinal fluid following treatment initiation with antisense oligonucleotide therapies in motor neuron diseases.

5q-associated spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS) are two distinct neurological disorders leading to degeneration of lower motor neurons. The antisense oligonucleotides (ASOs) nusinersen and tofersen are novel disease-modifying agents for these diseases, respectively. In the context of ASO treatment, the cytological characteristics and composition of cerebrospinal fluid (CSF) have recently garnered particular interest. This report presents a case series of CSF cytology findings in two patients with SMA and ALS revealing comparable unspecified macrophage inclusions following treatment initiation with nusinersen and tofersen. Yet, the presence of these "asophages" in the treatment course of two different ASOs is of unclear significance. While both treatments have been well tolerated, this phenomenon warrants attention, given the long-term nature of these treatments.

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CiteScore
7.40
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