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Dengue virus infection: Current concepts in immune mechanisms and lessons from murine models

机译:登革热病毒感染:免疫机制的最新概念和来自鼠模型的教训

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摘要

Dengue viruses (DENV), a group of four serologically distinct but related flaviviruses, are responsible for one of the most important emerging viral diseases. This mosquito-borne disease has a great impact in tropical and subtropical areas of the world in terms of illness, mortality and economic costs, mainly due to the lack of approved vaccine or antiviral drugs. Infections with one of the four serotypes of DENV (DENV-1-4) result in symptoms ranging from an acute, self-limiting febrile illness, dengue fever, to severe dengue haemorrhagic fever or dengue shock syndrome. We reviewed the existing mouse models of infection, including the DENV-2-adapted strain P23085. The role of CC chemokines, interleukin-17 (IL-17), IL-22 and invariant natural killer T cells in mediating the exacerbation of disease in immune-competent mice is highlighted. Investigations in both immune-deficient and immune-competent mouse models of DENV infection may help to identify key host-pathogen factors and devise novel therapies to restrain the systemic and local inflammatory responses associated with severe DENV infection.
机译:登革热病毒(DENV)是四种血清学上不同但相关的黄病毒,是最重要的新兴病毒性疾病之一。这种蚊虫传播的疾病在疾病,死亡率和经济成本方面对世界热带和亚热带地区产生巨大影响,这主要是由于缺乏批准的疫苗或抗病毒药物。 DENV四种血清型之一(DENV-1-4)的感染导致的症状从急性,自限性高热疾病,登革热到严重的登革出血热或登革热休克综合症。我们审查了现有的感染小鼠模型,包括适应DENV-2的品系P23085。强调了CC趋化因子,白介素17(IL-17),IL-22和不变的自然杀伤T细胞在介导免疫能力强的小鼠疾病恶化中的作用。对DENV感染的免疫缺陷和具有免疫能力的小鼠模型的研究可能有助于鉴定关键的宿主病原因子,并设计新的疗法来抑制与严重DENV感染相关的全身和局部炎症反应。

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