Etiology is the key determinant of neuroinflammation in epilepsy: Elevation of cerebrospinal fluid cytokines and chemokines in febrile infection-related epilepsy syndrome and febrile status epilepticus

被引:123
作者
Kothur, Kavitha [1 ,2 ]
Bandodkar, Sushil [3 ]
Wienholt, Louise [4 ]
Chu, Stephanie [4 ]
Pope, Alun [5 ]
Gill, Deepak [1 ,2 ]
Dale, Russell C. [1 ,2 ]
机构
[1] Univ Sydney, Neuroimmunol Grp, Kids Neurosci Ctr, Sydney, NSW, Australia
[2] Childrens Hosp Westmead, TY Nelson Dept Neurol & Neurosurg, Westmead, NSW, Australia
[3] Childrens Hosp Westmead, Dept Biochem, Westmead, NSW, Australia
[4] Royal Prince Alfred Hosp, Dept Clin Immunol, Camperdown, NSW, Australia
[5] Monash Univ, Eastern Hlth Clin Sch, Clayton, Vic, Australia
关键词
chemokine; cytokine; epilepsy; febrile infection-related epilepsy syndrome; febrile status epilepticus; inflammatory; INFLAMMATORY CYTOKINES; RAT HIPPOCAMPUS; GLIA ACTIVATION; ACUTE ENCEPHALOPATHY; ACUTE ENCEPHALITIS; ADAPTIVE IMMUNITY; SEIZURES; BRAIN; EPILEPTOGENESIS; BIOMARKERS;
D O I
10.1111/epi.16275
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To investigate intrathecal inflammation using cerebrospinal fluid (CSF) cytokines and chemokines in a subgroup of pediatric epilepsy patients with frequent daily seizures. Methods 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. Results 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-alpha, 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. Significance 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.
引用
收藏
页码:1678 / 1688
页数:11
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