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利用动物模型理解寨卡病毒感染的发病机制

Understanding the Pathogenesis of Zika Virus Infection Using Animal Models.

作者信息

Krause Keeton K, Azouz Francine, Shin Ok Sarah, Kumar Mukesh

机构信息

Department of Tropical Medicine, Medical Microbiology and Pharmacology, Pacific Center for Emerging Infectious Diseases Research, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, HI 96813, USA.

Department of Biomedical Sciences, Korea University College of Medicine, Seoul 02841, Korea.

出版信息

Immune Netw. 2017 Oct;17(5):287-297. doi: 10.4110/in.2017.17.5.287. Epub 2017 Oct 19.

Abstract

Zika virus (ZIKV) is a member of family that has emerged as a pathogen of significant public health importance. The rapid expansion of ZIKV in the South and Central America has recently gained medical attention emphasizing the capacity of ZIKV to spread to non-endemic regions. ZIKV infection during pregnancy has been demonstrated to cause microcephaly and other fetal developmental abnormalities. An increased incidence of Guillain-Barre syndrome, an immune mediated neuropathy of the peripheral nervous system, has also been reported in ZIKV-infected patients in French Polynesia and Brazil. No effective therapies currently exist for treating patients infected with ZIKV. Despite the relatively short time interval, an intensive effort by the global scientific community has resulted in development of animal models to study multiple aspects of ZIKV biology. Several animal models have been established to investigate pathogenesis of ZIKV in adults, pregnant mothers, and developing fetuses. Here we review the remarkable progress of newly developed small and large animal models for understanding ZIKV pathogenesis.

摘要

寨卡病毒(ZIKV)是一种已成为具有重大公共卫生意义的病原体的病毒家族成员。寨卡病毒在南美洲和中美洲的迅速传播最近引起了医学界的关注,凸显了其传播到非流行地区的能力。孕期感染寨卡病毒已被证实会导致小头畸形和其他胎儿发育异常。在法属波利尼西亚和巴西,寨卡病毒感染患者中也报告了格林-巴利综合征(一种外周神经系统的免疫介导性神经病变)发病率增加。目前尚无有效疗法治疗寨卡病毒感染患者。尽管时间间隔相对较短,但全球科学界的密集努力已促成用于研究寨卡病毒生物学多个方面的动物模型的开发。已经建立了几种动物模型来研究寨卡病毒在成人、怀孕母亲和发育中的胎儿中的发病机制。在此,我们综述新开发的小型和大型动物模型在理解寨卡病毒发病机制方面取得的显著进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92d5/5662778/21d312614299/in-17-287-g001.jpg

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