Kitab Bouchra, Kohara Michinori, Tsukiyama-Kohara Kyoko
Joint Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima, 890-0065, Japan.
Department of Microbiology and Cell Biology, Tokyo Metropolitan Institute of Medical Science, Tokyo, 156-8506, Japan.
Arch Virol. 2018 Jul;163(7):1717-1726. doi: 10.1007/s00705-018-3784-z. Epub 2018 Mar 8.
Dengue is the most prevalent arboviral disease in humans and leads to significant morbidity and socioeconomic burden in tropical and subtropical areas. Dengue is caused by infection with any of the four closely related serotypes of dengue virus (DENV1-4) and usually manifests as a mild febrile illness, but may develop into fatal dengue hemorrhagic fever and shock syndrome. There are no specific antiviral therapies against dengue because understanding of DENV biology is limited. A tetravalent chimeric dengue vaccine, Dengvaxia, has finally been licensed for use, but its efficacy was significantly lower against DENV-2 infections and in dengue-naïve individuals. The identification of mechanisms underlying the interactions between DENV and immune responses will help to determine efficient therapeutic and preventive options. It has been well established how the innate immune system responds to DENV infection and how DENV overcomes innate antiviral defenses, however further progress in this field remains hampered by the absence of appropriate experimental dengue models. Herein, we review the available in vitro and in vivo approaches to study the innate immune responses to DENV.
登革热是人类中最普遍的虫媒病毒病,在热带和亚热带地区导致了严重的发病率和社会经济负担。登革热由感染四种密切相关的登革病毒血清型(DENV1 - 4)中的任何一种引起,通常表现为轻度发热疾病,但可能发展为致命的登革出血热和休克综合征。由于对登革病毒生物学的了解有限,目前尚无针对登革热的特异性抗病毒疗法。一种四价嵌合登革热疫苗Dengvaxia最终已获许可使用,但其对DENV - 2感染以及初次感染登革热的个体的疗效显著较低。确定登革病毒与免疫反应之间相互作用的潜在机制将有助于确定有效的治疗和预防方案。关于固有免疫系统如何应对登革病毒感染以及登革病毒如何克服固有抗病毒防御,已经有了充分的研究,然而,由于缺乏合适的实验性登革热模型,该领域的进一步进展仍然受到阻碍。在此,我们综述了现有的用于研究对登革病毒固有免疫反应的体外和体内方法。