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格尔德霉素可减轻急性呼吸窘迫综合征并提高感染高致病性H5N1流感病毒小鼠的存活率。

Geldanamycin Reduces Acute Respiratory Distress Syndrome and Promotes the Survival of Mice Infected with the Highly Virulent H5N1 Influenza Virus.

作者信息

Wang Chengmin, Liu Pengpeng, Luo Jing, Ding Hua, Gao Yan, Sun Lei, Luo Fubing, Liu Xiaodong, He Hongxuan

机构信息

National Research Center for Wildlife Borne Diseases, Institute of Zoology, Chinese Academy of SciencesBeijing, China.

Department of Infectious Diseases, Hangzhou Center for Disease Control and PreventionHangzhou, China.

出版信息

Front Cell Infect Microbiol. 2017 Jun 15;7:267. doi: 10.3389/fcimb.2017.00267. eCollection 2017.

Abstract

Infections with lethal influenza viruses lead to acute lung injury (ALI) or acute respiratory distress syndrome (ARDS), which may be related to the activation of the host's immune system. Here, in our study, male C57BL/6 mice were infected with 10 LD of the H5N1 influenza virus and treated with geldanamycin or oseltamivir 2 h after infection. Lung injury was assessed by histopathology on days 4 and 7. The viral load was quantified by measuring the NP gene expression level on days 2, 4, and 7. Levels of cytokines and chemokines in bronchoalveolar lavage fluids and inflammatory cells were analyzed at different time points. Geldanamycin administration prolonged survival in mice and dramatically reduced lung injury and pulmonary inflammatory compared with other mice. Viral loads in geldanamycin-treated mice also significantly reduced compared with non-treated mice, but not to the extent as the oseltamivir-treated mice. Furthermore, the geldanamycin treatment markedly reduced the production of major proinflammatory cytokines and chemokines and attenuated the infiltration and activation of immune cells, but it did not alter the generation of virus-neutralizing antibodies. In conclusion, geldanamycin plays an important role in attenuating virus infection-induced ALI/ARDS by reducing the host's inflammatory responses and may provide an important reference for clinical treatments.

摘要

感染致死性流感病毒会导致急性肺损伤(ALI)或急性呼吸窘迫综合征(ARDS),这可能与宿主免疫系统的激活有关。在此,在我们的研究中,雄性C57BL/6小鼠感染10个半数致死量的H5N1流感病毒,并在感染后2小时用格尔德霉素或奥司他韦进行治疗。在第4天和第7天通过组织病理学评估肺损伤情况。在第2天、第4天和第7天通过测量NP基因表达水平来定量病毒载量。在不同时间点分析支气管肺泡灌洗液中的细胞因子和趋化因子水平以及炎症细胞情况。与其他小鼠相比,给予格尔德霉素可延长小鼠存活时间,并显著减轻肺损伤和肺部炎症。与未治疗的小鼠相比,接受格尔德霉素治疗的小鼠的病毒载量也显著降低,但降低程度不如接受奥司他韦治疗的小鼠。此外,格尔德霉素治疗显著降低了主要促炎细胞因子和趋化因子的产生,并减弱了免疫细胞的浸润和激活,但并未改变病毒中和抗体的产生。总之,格尔德霉素通过减轻宿主的炎症反应在减轻病毒感染诱导的ALI/ARDS中发挥重要作用,可能为临床治疗提供重要参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d42e/5471324/b9f8172dab62/fcimb-07-00267-g0001.jpg

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