Multiple organ infection and the pathogenesis of SARS

Jiang Gu(State University of New York), Encong Gong(Peking University), Bo Zhang(Peking University), Jie Zheng(Peking University), Zifen Gao(Peking University), Yanfeng Zhong(Peking University), Wan-zhong Zou(Peking University), Jun Zhan(Peking University), Shenglan Wang(Peking University), Zhigang Xie(Peking University), Hui Zhuang(Peking University), Bingquan Wu(Peking University), Hao‐hao Zhong(Peking University), Hongquan Shao(Peking University), Weigang Fang(Peking University), Dongshia Gao(Peking University), Fei Pei(Peking University), Xingwang Li(Beijing Ditan Hospital), Zhongpin He(Beijing Ditan Hospital), Danzhen Xu(Beijing Ditan Hospital), X SHI(Peking University), Virginia Anderson(State University of New York), Anthony S.‐Y. Leong(University of Newcastle Australia)
The Journal of Experimental Medicine
July 25, 2005
Cited by 1,431Open Access
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Abstract

After >8,000 infections and >700 deaths worldwide, the pathogenesis of the new infectious disease, severe acute respiratory syndrome (SARS), remains poorly understood. We investigated 18 autopsies of patients who had suspected SARS; 8 cases were confirmed as SARS. We evaluated white blood cells from 22 confirmed SARS patients at various stages of the disease. T lymphocyte counts in 65 confirmed and 35 misdiagnosed SARS cases also were analyzed retrospectively. SARS viral particles and genomic sequence were detected in a large number of circulating lymphocytes, monocytes, and lymphoid tissues, as well as in the epithelial cells of the respiratory tract, the mucosa of the intestine, the epithelium of the renal distal tubules, the neurons of the brain, and macrophages in different organs. SARS virus seemed to be capable of infecting multiple cell types in several organs; immune cells and pulmonary epithelium were identified as the main sites of injury. A comprehensive theory of pathogenesis is proposed for SARS with immune and lung damage as key features.


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