Calderón-Peláez María-Angélica, Velandia-Romero Myriam L, Bastidas-Legarda Leidy Y, Beltrán Edgar O, Camacho-Ortega Sigrid J, Castellanos Jaime E
Laboratorio de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Front Microbiol. 2019 Jun 26;10:1435. doi: 10.3389/fmicb.2019.01435. eCollection 2019.
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.
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。