Molecular pathology of emerging coronavirus infections

被引:228
作者
Gralinski, Lisa E. [1 ]
Baric, Ralph S. [1 ,2 ]
机构
[1] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
SARS-CoV; MERS-CoV; coronavirus; acute respiratory distress syndrome; ARDS; acute lung injury; type II pneumocytes; ACUTE RESPIRATORY SYNDROME; SARS-LIKE CORONAVIRUS; CLINICAL-FEATURES; MERS-CORONAVIRUS; COAGULATION CASCADE; PULMONARY PATHOLOGY; ACCESSORY PROTEINS; DISTRESS-SYNDROME; IMMUNE-RESPONSES; DROMEDARY CAMELS;
D O I
10.1002/path.4454
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Respiratory viruses can cause a wide spectrum of pulmonary diseases, ranging from mild, upper respiratory tract infections to severe and life-threatening lower respiratory tract infections, including the development of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). Viral clearance and subsequent recovery from infection require activation of an effective host immune response; however, many immune effector cells may also cause injury to host tissues. Severe acute respiratory syndrome (SARS) coronavirus and Middle East respiratory syndrome (MERS) coronavirus cause severe infection of the lower respiratory tract, with 10% and 35% overall mortality rates, respectively; however, >50% mortality rates are seen in the aged and immunosuppressed populations. While these viruses are susceptible to interferon treatment in vitro, they both encode numerous genes that allow for successful evasion of the host immune system until after high virus titres have been achieved. In this review, we discuss the importance of the innate immune response and the development of lung pathology following human coronavirus infection. (c) 2014 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
引用
收藏
页码:185 / 195
页数:11
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