Unit of Microbiology and Molecular Biology, ICMR-Vector Control Research Center, Puducherry, India,
Unit of Microbiology and Molecular Biology, ICMR-Vector Control Research Center, Puducherry, India.
Neuroimmunomodulation. 2019;26(3):111-118. doi: 10.1159/000501209. Epub 2019 Jul 26.
Neuroinflammation (inflammation in brain) has been known to play an important role in the development of dengue virus disease. Recently, studies from both clinical and experimental models suggest the involvement of neuroinflammation in dengue viral disease. Studies in clinical setup demonstrated that, microglial cells are actively involved in the patients having dengue virus infection, showing involvement of innate immune response in neuroinflammation. It was further proved that, clinical isolates of dengue-2 virus were able to initiate the pathologic response when injected in the mice brain. Natural killer cells were also found to play a crucial role to activate adaptive immune response. Notably, CXCL10/IFN-inducible protein 10 and CXCR3 are involved in dengue virus-mediated pathogenesis and play an important role in the development of dengue virus-mediated paralysis. In a latest report, it was seen that intracranial injection of dengue virus increases the CD8+ T-cell infiltration in brain, showing an important mechanism of neuroinflammation during the dengue virus infection. A similar study has described that, when DENV-3 is injected into the mice, it enhances the infiltration of CD8+ and CD4+ T cells as well as neutrophils. Cells immune-reactive against NS3 antigen were found throughout the brain. In conclusion, we focus on the various molecular mechanisms which contribute to the basic understanding about the role of neuroinflammation in dengue fever. These mechanisms will help in better understanding dengue pathophysiology and thus help in the development of possible therapeutics.
神经炎症(大脑中的炎症)已被证实对登革热病毒病的发展起着重要作用。最近,来自临床和实验模型的研究表明,神经炎症参与了登革热病毒病。临床研究表明,在感染登革热病毒的患者中,小胶质细胞积极参与其中,表现出固有免疫反应参与神经炎症。进一步证明,当将登革热 2 型病毒的临床分离株注射到小鼠大脑中时,它们能够引发病理反应。自然杀伤细胞也被发现对激活适应性免疫反应起着至关重要的作用。值得注意的是,CXCL10/IFN 诱导蛋白 10 和 CXCR3 参与登革病毒介导的发病机制,并在登革病毒介导的麻痹发展中发挥重要作用。在最新的一份报告中,人们发现,脑内注射登革病毒会增加大脑中 CD8+T 细胞的浸润,这表明在登革病毒感染期间存在重要的神经炎症机制。一项类似的研究表明,当将 DENV-3 注入小鼠体内时,它会增强 CD8+和 CD4+T 细胞以及中性粒细胞的浸润。在整个大脑中都发现了针对 NS3 抗原的免疫反应细胞。总之,我们专注于有助于深入了解神经炎症在登革热中的作用的各种分子机制。这些机制将有助于更好地理解登革热病理生理学,从而有助于开发可能的治疗方法。