Pathogenetic mechanisms of severe acute respiratory syndrome

被引:135
作者
Guo, Yong [1 ]
Korteweg, Christine [1 ]
McNutt, Michael A. [1 ]
Gu, Jiang [1 ]
机构
[1] Peking Univ, Ctr Infect Dis, Sch Med Sci, Dept Pathol, Beijing 100083, Peoples R China
关键词
SARS; pathology; immune system; virus; lung;
D O I
10.1016/j.virusres.2007.01.022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Severe acute respiratory syndrome (SARS) is an acute respiratory disease with significant morbidity and mortality. While its clinical manifestations have been extensively studied, its pathogenesis is not yet fully understood. A limited number of autopsy studies have revealed that the lungs and the immune system are the organs that sustain the most severe damage. Other organs affected include the kidneys, brain, digestive tract, heart. liver, thyroid gland and urogenital tract. The primary target cells are pneumocytes and enterocytes, both cell types abundantly expressing angiotensin-converting enzyme 2 which is the main SARS-CoV receptor. Other cell types infected include the epithelial cells of renal tubules, cerebral neurons, and immune cells. The pathology of this disease results from both direct and indirect injury. Direct injury is caused by infection of the tar-et cells by the virus. Indirect injury mainly results from immune responses, circulatory dysfunction, and hypoxia. In this review, we summarize the major pathological findings at the gross, cellular and molecular levels and discuss the various possible mechanisms that may contribute to the pathogenesis of SARS. The implications of the proposed pathogenesis for prevention, diagnosis and therapy of the disease are discussed. (C) 2007 Published by Elsevier B.V.
引用
收藏
页码:4 / 12
页数:9
相关论文
共 72 条
[1]   Pathogenesis of human immunodeficiency virus-induced neurological disease [J].
Albright, AV ;
Soldan, SS ;
González-Scarano, F .
JOURNAL OF NEUROVIROLOGY, 2003, 9 (02) :222-227
[2]   Clinical significance of hepatic derangement in severe acute respiratory syndrome [J].
Chan, Henry Lik-Yuen ;
Kwan, Ambrose Chi-Pong ;
To, Ka-Fai ;
Lai, Sik-To ;
Chan, Paul Kay-Sheung ;
Leung, Wai-Keung ;
Lee, Nelson ;
Wu, Alan ;
Sung, Joseph Jao-Yiu .
WORLD JOURNAL OF GASTROENTEROLOGY, 2005, 11 (14) :2148-2153
[3]   Detection of SARS coronavirus in patients with suspected SARS [J].
Chan, KH ;
Poon, LLLM ;
Cheng, VCC ;
Guan, Y ;
Hung, IFN ;
Kong, J ;
Yam, LYC ;
Seto, WH ;
Yuen, KY ;
Peiris, JSM .
EMERGING INFECTIOUS DISEASES, 2004, 10 (02) :294-299
[4]   Homozygous L-SIGN (CLEC4M) plays a protective role in SARS coronavirus infection [J].
Chan, VSF ;
Chan, KYK ;
Chen, YX ;
Poon, LLM ;
Cheung, ANY ;
Zheng, BJ ;
Chan, KH ;
Mak, W ;
Ngan, HYS ;
Xu, XN ;
Screaton, G ;
Tam, PKH ;
Austyn, JM ;
Chan, LC ;
Yip, SP ;
Peiris, M ;
Khoo, US ;
Lin, CLS .
NATURE GENETICS, 2006, 38 (01) :38-46
[5]  
CHANG JW, 2003, THORAX, V58, P689
[6]   SARS-associated viral hepatitis caused by a novel coronavirus: Report of three cases [J].
Chau, TN ;
Lee, KC ;
Yao, H ;
Tsang, TY ;
Chow, TC ;
Yeung, YC ;
Choi, KW ;
Tso, YK ;
Lau, T ;
Lai, ST ;
Lai, CL .
HEPATOLOGY, 2004, 39 (02) :302-310
[7]   Viral shedding patterns of coronavirus in patients with probable severe acute respiratory syndrome [J].
Cheng, PKC ;
Wong, DA ;
Tong, LKL ;
Ip, SM ;
Lo, ACT ;
Lau, CS ;
Yeung, EYH ;
Lim, WWL .
LANCET, 2004, 363 (9422) :1699-1700
[8]   Cytokine responses in severe acute respiratory syndrome coronavirus-infected macrophages in vitro: possible relevance to pathogenesis [J].
Cheung, CY ;
Poon, LLM ;
Ng, IHY ;
Luk, W ;
Sia, SF ;
Wu, MHS ;
Chan, KH ;
Yuen, KY ;
Gordon, S ;
Guan, Y ;
Peiris, JSM .
JOURNAL OF VIROLOGY, 2005, 79 (12) :7819-7826
[9]   The spectrum of pathological changes in severe acute respiratory syndrome (SARS) [J].
Cheung, OY ;
Chan, JWM ;
Ng, CK ;
Koo, CK .
HISTOPATHOLOGY, 2004, 45 (02) :119-124
[10]   Detection of severe acute respiratory syndrome-associated coronavirus in pneumocytes of the lung [J].
Chow, KC ;
Hsiao, CH ;
Lin, TY ;
Chen, CL ;
Chiou, SH .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2004, 121 (04) :574-580