Early central vs. peripheral immunological and neurobiological effects of fingolimod-a longitudinal study.

IF 4.2
Tony Sehr, Katja Akgün, Undine Proschmann, Robert Bucki, Malgorzata Zendzian-Piotrowska, Tjalf Ziemssen
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引用次数: 9

Abstract

Fingolimod (FTY) is known to have multiple effects on the immune system and the central nervous system (CNS) in patients with multiple sclerosis (MS). In this study, we evaluated the immunological and neurobiological effects of FTY in MS. Blood and cerebrospinal fluid (CSF) samples were collected from 15 MS patients before first FTY administration and after 4 months of FTY therapy. Immunophenotyping and evaluation of sphingosine-1-phosphate (S1P), neurofilament light chain (NFL), S-100 and neuron-specific enolase (NSE) levels were conducted. After 4 months of FTY therapy, absolute cell count in CSF was decreased from 6.33 to 2.43 MPt/l, accompanied by decreases of CD3+ (2.22 to 0.65 MPt/l) and of CD4+ counts (1.60 to 0.39 MPt/l). In blood, CD3+ (1.05 to 0.09 GPt/l), CD4+ (0.80 to 0.02 GPt/l), CD8+ (0.23 to 0.04 GPt/l) and CD19+ (0.21 to 0.01GPt/l) cell counts were as well reduced. CD14+ cell count remained stable over the same period (0.24 to 0.26GPt/l). NFL and S1P levels in CSF and blood were reduced over time (NFL: CSF 1759 to 1359 pg/l, blood 8.42 to 7.36 pg/l; S1P: CSF 2.12 to 0.71 nmol/l, blood 392.1 to 312.9 nmol/l). Strong correlations between CSF and blood NFL levels were observed. Neuronal damage markers such as S-100 (1.86 to 1.69 μg/l) and NSE (9.53 to 8.67 μg/l) were reduced to a lesser degree than other markers. FTY exerted significant effects on immunological and neurobiological markers in the central and peripheral compartment. Decreases in levels of neuroinflammatory and neurodegenerative markers were already evident after 4 months of treatment. Four-month serum NFL level appears to be a useful marker for FTY efficacy that correlates well with changes in the CNS compartment. KEY MESSAGES: FTY has important immunological effects in both central and peripheral compartments. Cellular effects of FTY effects are more pronounced in the blood than in the CSF. FTY reduces S1P and NFL levels in CSF and serum. Serum NFL appears to be a useful marker for FTY therapy.

芬戈莫德的早期中枢与外周免疫和神经生物学效应——一项纵向研究。
Fingolimod (FTY)已知对多发性硬化症(MS)患者的免疫系统和中枢神经系统(CNS)有多重影响。在这项研究中,我们评估了FTY在MS中的免疫和神经生物学作用,收集了15例MS患者在第一次给药前和治疗4个月后的血液和脑脊液(CSF)样本。免疫分型并评价鞘氨醇-1-磷酸(S1P)、神经丝轻链(NFL)、S-100和神经元特异性烯醇化酶(NSE)水平。治疗4个月后,脑脊液细胞绝对计数从6.33下降到2.43 MPt/l, CD3+(2.22下降到0.65 MPt/l)和CD4+(1.60下降到0.39 MPt/l)下降。血液中CD3+ (1.05 ~ 0.09 GPt/l)、CD4+ (0.80 ~ 0.02 GPt/l)、CD8+ (0.23 ~ 0.04 GPt/l)、CD19+ (0.21 ~ 0.01GPt/l)细胞计数均降低。CD14+细胞计数在同一时期保持稳定(0.24 ~ 0.26GPt/l)。随着时间的推移,脑脊液和血液中的NFL和S1P水平降低(NFL: CSF 1759至1359 pg/l,血8.42至7.36 pg/l;S1P: CSF 2.12 ~ 0.71 nmol/l,血392.1 ~ 312.9 nmol/l)。观察到脑脊液和血液NFL水平之间存在很强的相关性。神经损伤标志物S-100 (1.86 ~ 1.69 μg/l)和NSE (9.53 ~ 8.67 μg/l)的降低程度较其他标志物较轻。FTY对中央和外周腔室的免疫和神经生物学指标有显著影响。治疗4个月后,神经炎症和神经退行性标志物水平明显下降。4个月血清NFL水平似乎是衡量FTY疗效的有用指标,它与中枢神经系统室的变化密切相关。关键信息:FTY在中央和外周细胞室都有重要的免疫作用。FTY效应的细胞效应在血液中比在脑脊液中更为明显。FTY降低CSF和血清中S1P和NFL水平。血清NFL似乎是一个有用的标志,以治疗FTY。
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