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Current immunotherapies for multiple sclerosis and neuromyelitis optica spectrum disorders: the similarities and differences 目前多发性硬化症和视神经脊髓炎谱系障碍的免疫疗法的异同
Pub Date : 2019-05-16 DOI: 10.20517/2347-8659.2019.06
Lujun Zhang, Jingyuan Tian, Bin Li
Multiple sclerosis (MS) and neuromyelitis optica spectrum disorders (NMOSD) are autoimmune demyelinating diseases of the central nervous system. Neuromyelitis optica was considered a variant of MS until the discovery of NMO-IgG in 2004, which changed our understanding of the pathophysiology of NMOSD. This review focuses on the similarities and differences in the immune treatments of MS and NMOSD.
多发性硬化症(MS)和视神经脊髓炎谱系障碍(NMOSD)是中枢神经系统自身免疫性脱髓鞘疾病。在2004年发现NMO-IgG之前,视神经脊髓炎一直被认为是多发性硬化症的一种变体,这改变了我们对NMOSD病理生理的认识。本文就MS与NMOSD免疫治疗的异同作一综述。
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引用次数: 7
Bartonella henselae neuroretinitis in a patient without cat scratch 无猫抓伤的亨塞拉巴尔通体神经视网膜炎1例
Pub Date : 2019-04-24 DOI: 10.20517/2347-8659.2019.09
Claudia Montabone, D. Vecchio, S. Vujosevic, S. D. Cillà, R. Cantello
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引用次数: 1
The involvement of anti-neurofascin 155 antibodies in central and peripheral demyelinating diseases 抗神经筋膜素155抗体在中枢和外周脱髓鞘疾病中的作用
Pub Date : 2019-04-08 DOI: 10.20517/2347-8659.2019.08
M. Gonçalves, Y. Fragoso
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引用次数: 0
Speedy/RINGO: a molecular savior in spinal cord injury-based neurodegeneration? Speedy/RINGO:脊髓损伤性神经变性的分子救星?
Pub Date : 2019-03-28 DOI: 10.20517/2347-8659.2018.70
Yeşim Kaya, A. Yıldız
Endogenous or exogenous insults can cause spinal cord injury (SCI), often resulting in the loss of motor, autonomic, sensory and reflex functions. The pathogenesis of SCI comprises two stages. The primary injury stage occurs at the moment of trauma and is characterized by hemorrhage and rapid cell death. The secondary injury stage occurs due to progression of primary damage and is characterized by tissue loss and functional disorder. One of the most important cellular mechanisms underlying secondary injury is glutamate excitotoxicity, which overactivates the calpain protease via excessive Ca influx and induces neuronal apoptosis via p53 induction. Furthermore, Ca influx elicits apoptosis by inducing p53, thus negatively affecting two pathways: the mitogenic extracellular signal-regulated kinase/mitogenactivated protein kinase (ERK/MAPK) pathway and the survival phosphoinositide 3-kinase/protein kinase B (PI3K/AKT) pathway. Speedy/rapid inducer of G2/M progression in oocytes (Speedy/RINGO) is a cell cycle regulatory protein that increases survival of p53-positive mitotic cells by inhibiting the apoptotic machinery. Moreover, this protein elicits p53dependent anti-apoptotic effects on calpain-induced degeneration of primary hippocampal neurons, amyotrophic lateral sclerosis motor neurons, and astrocytes and microglia in spinal cord lesions. The pathophysiology of SCI has not been fully elucidated and this hinders the development of powerful therapeutic strategies. This review focuses on the cellular mechanisms underlying the anti-apoptotic effects of Speedy/RINGO and discusses how this protective function can possibly be exploited to facilitate recovery from SCI. Particular attention is paid to reversal of the negative effects on the ERK/MAPK and PI3K/AKT pathways via induction of p53.
内源性或外源性损伤可引起脊髓损伤(SCI),通常导致运动、自主、感觉和反射功能的丧失。脊髓损伤的发病机制包括两个阶段。原发性损伤阶段发生在创伤瞬间,以出血和细胞快速死亡为特征。继发性损伤阶段是由于原发性损伤的进展而发生的,其特征是组织损失和功能障碍。继发性损伤最重要的细胞机制之一是谷氨酸兴奋性毒性,它通过过量的钙内流过度激活钙蛋白酶,并通过p53诱导诱导神经元凋亡。此外,Ca内流通过诱导p53诱导细胞凋亡,从而对两条途径产生负面影响:有丝分裂细胞外信号调节激酶/有丝分裂原活化蛋白激酶(ERK/MAPK)途径和存活磷酸肌苷3激酶/蛋白激酶B (PI3K/AKT)途径。卵母细胞G2/M进程快速诱导因子(Speedy/RINGO)是一种细胞周期调节蛋白,通过抑制凋亡机制提高p53阳性有丝分裂细胞的存活率。此外,该蛋白对calpain诱导的海马原代神经元、肌萎缩侧索硬化症运动神经元、脊髓病变中的星形胶质细胞和小胶质细胞变性具有p53依赖的抗凋亡作用。脊髓损伤的病理生理学尚未完全阐明,这阻碍了有效治疗策略的发展。这篇综述着重于Speedy/RINGO抗凋亡作用的细胞机制,并讨论了这种保护功能如何可能被利用来促进脊髓损伤的恢复。特别关注的是通过诱导p53逆转对ERK/MAPK和PI3K/AKT通路的负面影响。
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引用次数: 0
Adiponectin: a pivotal role in the protection against cerebral ischemic injury 脂联素:在保护脑缺血损伤中的关键作用
Pub Date : 2019-03-22 DOI: 10.20517/2347-8659.2019.07
Ming-Hsiu Wu
© The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. Adiponectin: a pivotal role in the protection against cerebral ischemic injury
©作者2019。开放获取本文遵循知识共享署名4.0国际许可协议(https://creativecommons.org/licenses/by/4.0/),该协议允许不受限制地使用、共享、改编、分发和复制,以任何媒介或格式,用于任何目的,甚至商业目的,只要您适当地注明原作者和来源,提供知识共享许可协议的链接,并注明是否进行了更改。脂联素:在脑缺血损伤保护中起关键作用
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引用次数: 3
Pulsed intravenous corticosteroids in chronic inflammatory demyelinating polyneuropathy: why not? 脉冲静脉皮质类固醇治疗慢性炎症性脱髓鞘性多发性神经病:为什么不呢?
Pub Date : 2019-02-24 DOI: 10.20517/2347-8659.2019.05
D. Orsucci
© The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. Pulsed intravenous corticosteroids in chronic inflammatory demyelinating polyneuropathy: why not?
©作者2019。开放获取本文根据知识共享署名4.0国际许可证获得许可(https://creativecommons.org/licenses/by/4.0/),允许以任何媒介或格式,出于任何目的,甚至商业目的,不受限制地使用、共享、改编、分发和复制,只要您对原作者和来源给予适当的信任,提供到知识共享许可证的链接,并说明是否进行了更改。脉冲静脉皮质类固醇治疗慢性炎症性脱髓鞘性多发性神经病:为什么不呢?
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引用次数: 0
Immunotherapeutic approaches for treatment of brain tumors 脑肿瘤的免疫治疗方法
Pub Date : 2019-01-16 DOI: 10.20517/2347-8659.2018.67
T. Lichtor
© The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. Immunotherapeutic approaches for treatment of brain tumors
©作者2019。开放获取本文遵循知识共享署名4.0国际许可协议(https://creativecommons.org/licenses/by/4.0/),该协议允许不受限制地使用、共享、改编、分发和复制,以任何媒介或格式,用于任何目的,甚至商业目的,只要您适当地注明原作者和来源,提供知识共享许可协议的链接,并注明是否进行了更改。脑肿瘤的免疫治疗方法
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引用次数: 0
Microglial activation and polarization after subarachnoid hemorrhage 蛛网膜下腔出血后小胶质细胞的活化和极化
Pub Date : 2019-01-14 DOI: 10.20517/2347-8659.2018.52
Z. Zheng, Kwok Chu George Wong
Subarachnoid hemorrhage (SAH) is a devastating stroke type, with high mortality and morbidity. The neuroinflammatory response evolves over time from early brain injury to delayed cerebral deterioration. Microglia, the resident immune cells of the central nervous system, respond to the acute brain injury through activation and polarization. Microglia are able to polarize along two pathways, classic M1 and alternative M2, towards tissue injury and tissue repair respectively. The modulation of microglial activation has gained appreciation as a means to prevent the detrimental effects. In this review, we describe the progression of microglial polarization after SAH and summarize the key studies on mediators of microglial activation, including M1 and M2 specific microglial markers, transcription factors and key signaling pathways. Interactions between microglia and other cells are critical in modulating microglial activation and function, which are discussed as well. The preclinical application of microgliadependent treatments is presented, aiming for a better understanding of modulating microglial function and suggesting future investigation for therapeutic approaches.
蛛网膜下腔出血(SAH)是一种极具破坏性的中风类型,具有较高的死亡率和发病率。神经炎症反应随着时间的推移从早期脑损伤演变为延迟性脑退化。小胶质细胞是中枢神经系统的固有免疫细胞,通过激活和极化对急性脑损伤做出反应。小胶质细胞能够沿着两种途径极化,即经典的M1和替代的M2,分别朝向组织损伤和组织修复。小胶质细胞激活的调节作为一种防止有害影响的手段已经得到了重视。在这篇综述中,我们描述了SAH后小胶质细胞极化的进展,并总结了关于小胶质细胞激活介质的关键研究,包括M1和M2特异性小胶质细胞标记物、转录因子和关键信号通路。小胶质细胞和其他细胞之间的相互作用在调节小胶质细胞的激活和功能方面至关重要,这一点也进行了讨论。介绍了小胶质细胞依赖性治疗的临床前应用,旨在更好地了解调节小胶质细胞功能,并建议未来对治疗方法进行研究。
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引用次数: 24
Economic impact of traumatic spinal cord injuries in the United States. 美国创伤性脊髓损伤的经济影响。
Pub Date : 2019-01-01 Epub Date: 2019-07-20 DOI: 10.20517/2347-8659.2019.15
Christopher H Merritt, Matthew A Taylor, Caleb J Yelton, Swapan K Ray

Individuals having sustained traumatic spinal cord injury (TSCI) in the United States are living longer as compared to historical trends, thanks to an ever-evolving understanding of the nature of this injury. Despite this, multiple barriers to care for TSCI patients remain including variations in government-issued veteran insurance, privatized insurance, and among uninsured individuals. The United States alone experiences 12,000 new TSCI cases every year, many of these are found to occur in a growing proportion of elderly individuals. It is crucial to understand both the short-term direct costs as wells as the long-term rehabilitation costs required by these TSCI patients. The lifetime financial burden for those having sustained a TSCI can be immense for patients, insurance companies, and hospital systems alike. Among those with TSCI, re-hospitalization rates are high, leading to increased healthcare resource utilization within this specific patient population. Costs can quickly balloon into hundreds of thousands of dollars and cause a profound financial burden for these patients. This review article seeks to communicate an understanding of the current financial landscape surrounding TSCI patients. The authors will also examine the costs of acute emergency room surgical care such as American spinal injury association grade, hospital length of stay, as well as the timing delay between injury and surgical decompression. Long-term costs associated with TSCI such as rehabilitation, care of secondary comorbidities, and post-injury employment prospects will be examined as well. These costs will be framed from the patient's perspective as well as from both the hospital and insurance company's perspectives. It is hoped a complete understanding as to what makes TSCI such a medically and financially burdensome injury will allow for improved healthcare resource utilization in this population.

与历史趋势相比,美国患有持续性创伤性脊髓损伤(TSCI)的个体寿命更长,这要归功于对这种损伤性质的不断发展的理解。尽管如此,对TSCI患者的护理仍然存在多种障碍,包括政府发行的退伍军人保险、私有化保险和没有保险的个人之间的差异。仅在美国,每年就有12,000例新的TSCI病例,其中许多病例发生在老年人中所占比例越来越大。了解这些TSCI患者所需的短期直接成本和长期康复成本是至关重要的。对于患者、保险公司和医院系统来说,TSCI患者一生的经济负担可能是巨大的。在TSCI患者中,再住院率很高,导致这一特定患者群体的医疗资源利用率增加。费用可能会迅速膨胀到数十万美元,给这些患者带来沉重的经济负担。这篇综述文章旨在传达对当前围绕TSCI患者的财务状况的理解。作者还将研究急性急诊室手术护理的费用,如美国脊髓损伤协会分级、住院时间以及损伤和手术减压之间的时间延迟。与TSCI相关的长期成本,如康复、继发性合并症的护理和伤后就业前景也将被检查。这些费用将从病人的角度以及医院和保险公司的角度来确定。希望全面了解是什么使TSCI成为一种医疗和经济负担沉重的伤害,将有助于改善这一人群的医疗资源利用。
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引用次数: 42
Roles of miRNAs in spinal cord injury and potential therapeutic interventions. miRNA 在脊髓损伤中的作用及潜在的治疗干预措施。
Pub Date : 2019-01-01 Epub Date: 2019-10-17 DOI: 10.20517/2347-8659.2019.19
Badria Almurshidi, Wayne Carver, Geoff Scott, Swapan K Ray

Spinal cord injury (SCI) affects approximately 200,000 individuals per year worldwide. There are more than 27 million people worldwide living with long-term disability due to SCI. Historically, it was thought that the central nervous system (CNS) had little ability for regeneration; however, more recent studies have demonstrated potential for repair within the CNS. Because of this, there exists a renewed interest in the discovery of novel approaches to promote regeneration in the CNS including the spinal cord. It is important to know the roles of the microRNAs (miRNAs) in modulation of pathogenesis in SCI and the potentials of the miRNA-based clinical interventions for controlling post-injury symptoms and improving functional recovery. The miRNAs, which are non-coding RNAs with an average of 22 nucleotides in length, are post-transcriptional gene regulators that cause degradation of the target mRNAs and thus negatively control their translation. This review article focuses on current research related to miRNAs and their roles in modulating SCI symptoms, asserting that miRNAs contribute to critical post-SCI molecular processes including neuroplasticity, functional recovery, astrogliosis, neuropathic pain, inflammation, and apoptosis. In particular, miR-96 provides a promising therapeutic opportunity to improve the outcomes of clinical interventions, including the way SCI injuries are evaluated and treated.

全世界每年约有 20 万人受到脊髓损伤(SCI)的影响。全世界有超过 2700 万人因脊髓损伤而长期残疾。过去,人们认为中枢神经系统(CNS)几乎没有再生能力;然而,最近的研究表明,中枢神经系统具有修复潜力。因此,人们对发现促进中枢神经系统(包括脊髓)再生的新方法重新产生了兴趣。了解微小核糖核酸(miRNA)在调节 SCI 发病机制中的作用以及基于 miRNA 的临床干预在控制损伤后症状和改善功能恢复方面的潜力非常重要。miRNA 是平均长度为 22 个核苷酸的非编码 RNA,是转录后的基因调控因子,可导致目标 mRNA 降解,从而消极地控制其翻译。这篇综述文章重点介绍了目前有关 miRNA 及其在调节 SCI 症状方面作用的研究,认为 miRNA 对 SCI 后的关键分子过程(包括神经可塑性、功能恢复、星形胶质细胞增生、神经病理性疼痛、炎症和细胞凋亡)做出了贡献。特别是,miR-96 为改善临床干预的结果(包括 SCI 损伤的评估和治疗方法)提供了一个很有希望的治疗机会。
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引用次数: 0
期刊
Neuroimmunology and Neuroinflammation
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