Flotats-Bastardas Marina, Bitzan Lisa, Grell Charlotte, Martakis Kyriakos, Winter Benedikt, Zemlin Michael, Wurster Claudia D, Uzelac Zeljko, Weiß Claudia, Hahn Andreas
Department of Pediatric Neurology, Saarland University Medical Center, Saarland University, Homburg, Germany.
Department of Pediatric Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.
Front Neurol. 2023 Dec 13;14:1269406. doi: 10.3389/fneur.2023.1269406. eCollection 2023.
BACKGROUND/OBJECTIVE: Neurofilament light chain (NfL) has been proposed as a biomarker reflecting disease severity and therapy response in children with spinal muscular atrophy type 1 and 2 (SMA1 and 2). The objective of this study was to examine how serum NfL changes after gene replacement therapy (GRT) with onasemnogene abeparvovec-xioi.
We measured NfL in serum probes from 19 patients (10 SMA 1 and 6 SMA 2; 15 previously treated with nusinersen or risdiplam; 12 male) before and at variable time points after GRT. These values were related to motor scores (CHOP-Intend, HFMSE and RULM).
Median age at GRT was 19 months (range 2-46 months). Median NfL of all patients before GRT was 39 pg/ml (range 0-663 pg/ml; normal values <25 pg/ml), increased significantly to 297 pg/ml (range 61-1,696 pg/ml; p<0,002) 1 month after GRT, and decreased to 49 pg/ml (range 24-151 pg/ml) after 6 months. Subjects pre-treated with nusinersen or risdiplam had lower baseline NfL levels than naïve patients (p<0,005), but absolute increases of NfL were similar in both groups. While motor scores were improved in 14 out of 18 SMA patients (78%) 6 months after GRT NfL values differed not significantly from those measured at baseline (p = 0,959).
Serum NfL showed a paradoxical transient increase after GRT in both, pre-treated and naïve patients, which may reflect an immunological reaction in the CNS related to transfection of neuronal cells by AAV9. The clinical meaning of this increase should be assessed in future studies. Our findings encourage regular monitoring of NfL in OA treated patients.
背景/目的:神经丝轻链(NfL)已被提议作为反映1型和2型脊髓性肌萎缩症(SMA1和2)患儿疾病严重程度和治疗反应的生物标志物。本研究的目的是研究用onasemnogene abeparvovec-xioi进行基因替代治疗(GRT)后血清NfL如何变化。
我们在19例患者(10例SMA 1和6例SMA 2;15例先前接受过诺西那生或利司扑兰治疗;12例男性)接受GRT前及之后的不同时间点测量其血清样本中的NfL。这些值与运动评分(CHOP-Intend、HFMSE和RULM)相关。
GRT时的中位年龄为19个月(范围2-46个月)。所有患者在GRT前的NfL中位数为39 pg/ml(范围0-663 pg/ml;正常值<25 pg/ml),GRT后1个月显著升高至297 pg/ml(范围61-1,696 pg/ml;p<0.002),6个月后降至49 pg/ml(范围24-151 pg/ml)。先前接受过诺西那生或利司扑兰治疗的受试者基线NfL水平低于未接受过治疗的患者(p<0.005),但两组NfL的绝对升高相似。虽然18例SMA患者中有14例(78%)在GRT后6个月运动评分有所改善,但NfL值与基线时测量的值无显著差异(p = 0.959)。
在接受过治疗和未接受过治疗的患者中,血清NfL在GRT后均出现矛盾的短暂升高,这可能反映了中枢神经系统中与AAV9转染神经元细胞相关的免疫反应。这种升高的临床意义应在未来研究中评估。我们的发现鼓励对接受OA治疗的患者定期监测NfL。