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Description of high rates of unapparent and simultaneous multiple dengue virus infection in a Colombian jungle settlement.哥伦比亚丛林定居点登革热病毒隐性感染和同时多重感染的高发生率描述
Trop Biomed. 2016 Jun 1;33(2):375-382.
2
A (delayed) history of the brain lymphatic system.脑淋巴系统的(延迟)历史。
Nat Med. 2019 Apr;25(4):538-540. doi: 10.1038/s41591-019-0417-3.
3
Dengue.登革热。
Lancet. 2019 Jan 26;393(10169):350-363. doi: 10.1016/S0140-6736(18)32560-1.
4
Concurrent Guillain-Barré syndrome, transverse myelitis and encephalitis post-Zika: A case report and review of the pathogenic role of multiple arboviral immunity. Zika 病毒感染后并发格林-巴利综合征、横断性脊髓炎和脑炎:病例报告及多种虫媒病毒免疫的致病作用综述
J Neurol Sci. 2018 Dec 15;395:47-53. doi: 10.1016/j.jns.2018.09.028. Epub 2018 Sep 26.
5
West Nile Neuroinvasive Disease Presenting as Elsberg Syndrome.表现为埃尔斯伯格综合征的西尼罗河神经侵袭性疾病。
Neurologist. 2018 Sep;23(5):152-154. doi: 10.1097/NRL.0000000000000189.
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The First Case Report of West Nile Virus-Induced Acute Flaccid Quadriplegia in Canada.加拿大西尼罗河病毒引发急性弛缓性四肢瘫首例病例报告
Case Rep Infect Dis. 2018 Jul 15;2018:4361706. doi: 10.1155/2018/4361706. eCollection 2018.
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Astrogliopathology in the infectious insults of the brain.脑感染性损伤中的星形胶质细胞病理学
Neurosci Lett. 2019 Jan 10;689:56-62. doi: 10.1016/j.neulet.2018.08.003. Epub 2018 Aug 7.
8
Anti-TNF-α restricts dengue virus-induced neuropathy.抗 TNF-α 限制登革热病毒诱导的神经病。
J Leukoc Biol. 2018 Nov;104(5):961-968. doi: 10.1002/JLB.MA1217-484R. Epub 2018 Jul 25.
9
Tissue Specific Origin, Development, and Pathological Perspectives of Pericytes.周细胞的组织特异性起源、发育及病理学观点
Front Cardiovasc Med. 2018 Jun 27;5:78. doi: 10.3389/fcvm.2018.00078. eCollection 2018.
10
BALB/c mice infected with DENV-2 strain 66985 by the intravenous route display injury in the central nervous system.经静脉途径感染 DENV-2 株 66985 的 BALB/c 小鼠中枢神经系统受损。
Sci Rep. 2018 Jun 27;8(1):9754. doi: 10.1038/s41598-018-28137-y.

登革病毒感染血脑屏障细胞:重症疾病的后果

Dengue Virus Infection of Blood-Brain Barrier Cells: Consequences of Severe Disease.

作者信息

Calderón-Peláez María-Angélica, Velandia-Romero Myriam L, Bastidas-Legarda Leidy Y, Beltrán Edgar O, Camacho-Ortega Sigrid J, Castellanos Jaime E

机构信息

Laboratorio de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.

出版信息

Front Microbiol. 2019 Jun 26;10:1435. doi: 10.3389/fmicb.2019.01435. eCollection 2019.

DOI:10.3389/fmicb.2019.01435
PMID:31293558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6606788/
Abstract

More than 500 million people worldwide are infected each year by any of the four-dengue virus (DENV) serotypes. The clinical spectrum caused during these infections is wide and some patients may develop neurological alterations during or after the infection, which could be explained by the cryptic neurotropic and neurovirulent features of flaviviruses like DENV. Using and models, researchers have demonstrated that DENV can affect the cells from the blood-brain barrier (BBB) in several ways, which could result in brain tissue damage, neuronal loss, glial activation, tissue inflammation and hemorrhages. The latter suggests that BBB may be compromised during infection; however, it is not clear whether the damage is due to the infection or to the local and/or systemic inflammatory response established or activated by the BBB cells. Similarly, the kinetics and cascade of events that trigger tissue damage, and the cells that initiate it, are unknown. This review presents evidence of the BBB cell infection with DENV and the response established toward it by these cells; it also describes the consequences of this response on the nervous tissue, compares these evidence with the one reported with neurotropic viruses of the family, and shows the complexity and unpredictability of dengue and the neurological alterations induced by it. Clinical evidence and and models suggest that this virus uses the bloodstream to enter nerve tissue where it infects the different cells of the neurovascular unit. Each of the cell populations respond individually and collectively and control infection and inflammation, in other cases this response exacerbates the damage leaving irreversible sequelae or causing death. This information will allow us to understand more about the complex disease known as dengue, and its impact on a specialized and delicate tissue like is the nervous tissue.

摘要

全球每年有超过5亿人感染四种登革病毒(DENV)血清型中的任何一种。这些感染所引发的临床症状范围广泛,一些患者在感染期间或之后可能会出现神经功能改变,这可能是由登革病毒等黄病毒隐匿的嗜神经和神经毒性特征所解释的。利用[具体模型1]和[具体模型2]模型,研究人员已经证明,登革病毒可以通过多种方式影响血脑屏障(BBB)的细胞,这可能导致脑组织损伤、神经元丧失、神经胶质细胞活化、组织炎症和出血。后者表明在感染期间血脑屏障可能受到损害;然而,尚不清楚这种损害是由于感染本身还是由血脑屏障细胞建立或激活的局部和/或全身炎症反应所致。同样,引发组织损伤的事件动力学和级联反应以及引发损伤的细胞尚不清楚。本综述提供了登革病毒感染血脑屏障细胞以及这些细胞对其产生的反应的证据;它还描述了这种反应对神经组织的影响,将这些证据与[具体病毒家族]嗜神经病毒报道的证据进行了比较,并展示了登革热及其引发的神经功能改变的复杂性和不可预测性。临床证据以及[具体模型1]和[具体模型2]模型表明,这种病毒利用血流进入神经组织,在那里它感染神经血管单元的不同细胞。每个细胞群体单独和集体做出反应,控制感染和炎症,在其他情况下,这种反应会加剧损伤,留下不可逆转的后遗症或导致死亡。这些信息将使我们能够更深入地了解被称为登革热的复杂疾病,以及它对像神经组织这样特殊而脆弱的组织的影响。