Neuroimmunology Group, Kids Neuroscience Centre, The University of Sydney, Sydney, New South Wales, Australia.
T. Y. Nelson Department of Neurology and Neurosurgery, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
Epilepsia. 2019 Aug;60(8):1678-1688. doi: 10.1111/epi.16275. Epub 2019 Jul 8.
To investigate intrathecal inflammation using cerebrospinal fluid (CSF) cytokines and chemokines in a subgroup of pediatric epilepsy patients with frequent daily seizures.
We measured 32 cytokines/chemokines using multiplex immunoassay in CSF collected from pediatric patients with febrile infection-related epilepsy syndrome (FIRES)/FIRES-related disorders (FRD; n = 6), febrile status epilepticus (FSE; n = 8), afebrile status epilepticus (ASE; n = 8), and chronic epilepsy with frequent daily seizures (n = 21) and compared the results with noninflammatory neurological disorders (NIND; n = 20) and encephalitis (n = 43). We also performed longitudinal CSF cytokine/chemokine studies in three cases with FIRES/FRD.
The median age of onset of seizures was 2.4 years (range = 0.08-12.5). Median CSF timing from the onset of seizures was longer in chronic epilepsy (540 days), whereas FIRES, FSE, and ASE had CSF tested within 1-2 days of onset of seizures (P < .001). The elevation of cytokines/chemokines was higher in FIRES followed by FSE, when compared to chronic epilepsy and NIND controls. Th1-associated cytokines/chemokines (TNF-α, CXCL9, CXCL10, CXCL11), IL-6, CCL2, CCL19, and CXCL1 (P < .05) were elevated in FIRES, in contrast to the elevation of a broader network of cytokines/chemokines in encephalitis. The cytokines/chemokines (CXCL9, CXCL10, CXCL11, and CCL19) were elevated in FSE when compared to ASE despite the similar median seizure duration and timing of CSF testing in relation to seizures. Chronic epilepsy generally lacked significant elevation of cytokines/chemokines despite frequent daily seizures. The median concentrations of the cytokines/chemokines rapidly declined on serial testing during the course of illness in all three FIRES/FRD cases.
We identify significant differences in CSF cytokine/chemokine profile between FIRES/FRD and encephalitis. The prominent elevation of CSF cytokines and chemokines in FIRES/FRD and to a lesser extent FSE highlights that the cytokine/chemokine elevation is significantly associated with the etiology of the underlying process rather than purely reactive. However, it is unclear whether the immune activation contributes to the disease process.
通过测量脑脊液(CSF)中的细胞因子和趋化因子来研究鞘内炎症,这些细胞因子和趋化因子存在于患有频繁每日发作的儿科癫痫患者亚组中。
我们使用多重免疫分析法测量了 6 例发热感染相关癫痫综合征(FIRES)/FIRES 相关障碍(FRD)、8 例热性惊厥持续状态(FSE)、8 例无热惊厥持续状态(ASE)和 21 例慢性癫痫伴频繁每日发作(慢性癫痫)患者的 CSF 中的 32 种细胞因子/趋化因子,并将结果与非炎症性神经障碍(NIND)(20 例)和脑炎(43 例)进行比较。我们还对 3 例 FIRES/FRD 患者进行了 CSF 细胞因子/趋化因子的纵向研究。
癫痫发作的中位发病年龄为 2.4 岁(范围=0.08-12.5)。慢性癫痫的 CSF 时间中位数从癫痫发作开始时较长,而 FIRES、FSE 和 ASE 的 CSF 在癫痫发作后 1-2 天内进行检测(P<.001)。与慢性癫痫和 NIND 对照组相比,FIRES 中细胞因子/趋化因子的升高更高,其次是 FSE。与脑炎中细胞因子/趋化因子网络的广泛升高相比,FIRES 中升高了 Th1 相关细胞因子/趋化因子(TNF-α、CXCL9、CXCL10、CXCL11)、IL-6、CCL2、CCL19 和 CXCL1(P<.05)。与 ASE 相比,FSE 中细胞因子/趋化因子(CXCL9、CXCL10、CXCL11 和 CCL19)升高,尽管 CSF 检测与癫痫发作的中位持续时间和时间相似。慢性癫痫尽管频繁出现每日发作,但通常没有明显的细胞因子/趋化因子升高。在所有 3 例 FIRES/FRD 病例中,在疾病过程中进行的多次检测中,细胞因子/趋化因子的中位数浓度迅速下降。
我们发现 FIRES/FRD 和脑炎之间 CSF 细胞因子/趋化因子谱存在显著差异。FIRES/FRD 和在较小程度上 FSE 中 CSF 细胞因子和趋化因子的显著升高表明,细胞因子/趋化因子的升高与潜在过程的病因显著相关,而不仅仅是反应性的。然而,尚不清楚免疫激活是否有助于疾病进程。