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Mechanisms of Epileptogenesis in Pediatric Epileptic Syndromes: Rasmussen Encephalitis Infantile Spasms and Febrile Infection-related Epilepsy Syndrome (FIRES)

机译:小儿癫痫综合征的癫痫发生机理:拉斯姆森脑炎小儿痉挛和高热感染相关性癫痫综合征(FIRES)

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摘要

The mechanisms of epileptogenesis in pediatric epileptic syndromes are diverse, and may involve disturbances of neurodevelopmental trajectories, synaptic homeostasis, and cortical connectivity, which may occur during brain development, early infancy, or childhood. Although genetic or structural/metabolic factors are frequently associated with age-specific epileptic syndromes, such as infantile spasms and West syndrome, other syndromes may be determined by the effect of immunopathogenic mechanisms or energy-dependent processes in response to environmental challenges, such as infections or fever in normally-developed children during early or late childhood. Immune-mediated mechanisms have been suggested in selected pediatric epileptic syndromes in which acute and rapidly progressive encephalopathies preceded by fever and/or infections, such as febrile infection-related epilepsy syndrome, or in chronic progressive encephalopathies, such as Rasmussen encephalitis. A definite involvement of adaptive and innate immune mechanisms driven by cytotoxic CD8+ T lymphocytes and neuroglial responses has been demonstrated in Rasmussen encephalitis, although the triggering factor of these responses remains unknown. Although the beneficial response to steroids and adrenocorticotropic hormone of infantile spasms, or preceding fever or infection in FIRES, may support a potential role of neuroinflammation as pathogenic factor, no definite demonstration of such involvement has been achieved, and genetic or metabolic factors are suspected. A major challenge for the future is discovering pathogenic mechanisms and etiological factors that facilitate the introduction of novel targets for drug intervention aimed at interfering with the disease mechanisms, therefore providing putative disease-modifying treatments in these pediatric epileptic syndromes.Electronic supplementary materialThe online version of this article (doi:10.1007/s13311-014-0265-2) contains supplementary material, which is available to authorized users.
机译:小儿癫痫综合征的癫痫发生机理是多种多样的,并且可能涉及神经发育轨迹,突触稳态和皮质连接性的紊乱,这些紊乱可能发生在大脑发育,婴儿早期或儿童时期。尽管遗传或结构/代谢因素通常与特定年龄的癫痫综合征(如婴儿痉挛和West综合征)相关,但其他综合征可能是由免疫病理机制或能量依赖过程对环境挑战(如感染)的反应所决定的正常发育的儿童在儿童早期或晚期发烧或发烧。在某些小儿癫痫综合症中已提出了免疫介导的机制,其中急性和快速进行性脑病伴发烧和/或感染,如高热感染相关性癫痫综合征,或慢性进行性脑病,如拉斯穆森脑炎。在拉斯穆森脑炎中已经证实了由细胞毒性CD8 + T淋巴细胞和神经胶质反应驱动的适应性和先天性免疫机制的确定参与,尽管这些反应的触发因素仍然未知。尽管对婴儿痉挛,或先前发烧或感染FIRES的类固醇和促肾上腺皮质激素的有益反应可能支持神经炎症作为致病因素的潜在作用,但尚未明确证实这种参与,并怀疑有遗传或代谢因素。未来的主要挑战是发现致病机制和病因,以利于引入旨在干预疾病机制的新型药物干预靶标,从而为这些儿童癫痫综合症提供公认的缓解疾病的治疗方法。本文(doi:10.1007 / s13311-014-0265-2)包含补充材料,授权用户可以使用。

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