Author: To, KF; Lo, Anthony WI
Title: Exploring the pathogenesis of severe acute respiratory syndrome (SARS): the tissue distribution of the coronavirus (SARSâ€CoV) and its putative receptor, angiotensinâ€converting enzyme 2 (ACE2) Cord-id: kti44f0h Document date: 2004_6_21
ID: kti44f0h
Snippet: Severe acute respiratory syndrome (SARS) is an emerging infectious disease associated with a new coronavirus, SARSâ€CoV. Pulmonary involvement is the dominant clinical feature but extraâ€pulmonary manifestations are also common. Factors that account for the wide spectrum of organ system involvement and disease severity are poorly understood and the pathogenesis of SARSâ€CoV infection remains unclear. Angiotensin converting enzyme 2 (ACE2) has recently been identified as the functional cellula
Document: Severe acute respiratory syndrome (SARS) is an emerging infectious disease associated with a new coronavirus, SARSâ€CoV. Pulmonary involvement is the dominant clinical feature but extraâ€pulmonary manifestations are also common. Factors that account for the wide spectrum of organ system involvement and disease severity are poorly understood and the pathogenesis of SARSâ€CoV infection remains unclear. Angiotensin converting enzyme 2 (ACE2) has recently been identified as the functional cellular receptor for SARSâ€CoV. Studies of the tissue and cellular distribution of SARSâ€CoV, and ACE2 protein expression, reveal new insights into the pathogenesis of this deadly disease. ACE2 is expressed at high level in the primary target cells of SARSâ€CoV, namely pneumocytes and surface enterocytes of the small intestine. Despite the fact that SARSâ€CoV can infect the lung and intestine, the tissue responses in these two organs are different. All other tissues and cell types expressing ACE2 may be potential targets of SARSâ€CoV infection. Remarkably, endothelial cells, which express ACE2 to a high level, have not been shown to be infected by SARSâ€CoV. There is also evidence that cell types without detectable ACE2 expression may also be infected by the virus. Furthermore, studies in a new human cell culture model have indicated that the presence of ACE2 alone is not sufficient for maintaining viral infection. Therefore, other virus receptors or coâ€receptors may be required in different tissues. Moreover, the interaction between SARSâ€CoV and the immunological or lymphoid system remains to be defined. It is clear that we are only at the dawn of our understanding of the pathogenesis of SARS. As our knowledge of the pathogenic mechanisms improves, a more rational approach to therapeutic and vaccine development can be designed in order to combat this new and fatal human disease. Copyright © 2004 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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