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1.
J Exp Med ; 202(3): 415-24, 2005 Aug 01.
Article in English | MEDLINE | ID: mdl-16043521

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.


Subject(s)
Severe Acute Respiratory Syndrome/pathology , Severe acute respiratory syndrome-related coronavirus , Adult , Aged , Aged, 80 and over , Autopsy , Brain/pathology , Brain/virology , Female , Humans , Intestines/pathology , Intestines/virology , Kidney Tubules, Distal/pathology , Kidney Tubules, Distal/virology , Leukocytes/pathology , Leukocytes/virology , Lung , Lymphoid Tissue/pathology , Lymphoid Tissue/virology , Male , Middle Aged , Respiratory System/pathology , Respiratory System/virology , Retrospective Studies , Severe Acute Respiratory Syndrome/mortality , Severe Acute Respiratory Syndrome/virology
2.
Di Yi Jun Yi Da Xue Xue Bao ; 23(11): 1125-7, 2003 Nov.
Article in Chinese | MEDLINE | ID: mdl-14625166

ABSTRACT

OBJECTIVE: To explore the distribution of severe acute respiratory syndrome (SARS)-associated coronavirus (SARS-CoV) in SARS autopsy tissues at the molecular level. METHODS: In situ hybridization was used to detect the expression and location of SARS-CoV RNA polymerase gene in autopsy tissues from SARS-Cov-infected subjects, including the lung, spleen, lymph nodes, pituitary, pancreas, parathyroid, adrenal glands, gastrointestinal tract, skin, brain, liver, kidney, blood vessels, striated muscles of the limbs, bone marrow, heart, ovary, uterus and testicles. RESULT: SARS-CoV RNA was detected in the cytoplasm of the alveolar epithelia, infiltrating mononuclear phagocytes in the lungs, serous gland epithelium of the trachea/bronchus, monocytes in the spleen and lymph nodes, acinar cells in the pancreas, acidophilic cells in the parathyroid and pituitary, adrenal cortical cells, epithelia of the alimentary tracts, gastric parietal cells, sweat gland cells, brain neurons, hepatocytes near the central vein, epithelia of the distal renal tubules, bone marrow promyelocytes, and endothelia of the small veins. CONCLUSIONS: SARS-CoV invades various organs of the body and distributes in a similar fashion to CD13, the receptor of human coronavirus 229E. The detection of SARS-CoV in the sweat glands, alimentary tracts and epithelia of the distal convoluted tubules of the kidney may help identify the transmission routes of SARS-CoV.


Subject(s)
In Situ Hybridization/methods , RNA, Viral/analysis , Severe acute respiratory syndrome-related coronavirus/isolation & purification , Autopsy , Humans , Kidney Tubules, Distal/virology , Severe acute respiratory syndrome-related coronavirus/genetics , Severe Acute Respiratory Syndrome/diagnosis , Severe Acute Respiratory Syndrome/transmission , Sweat Glands/virology
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