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Issue 1067 coverUnderstanding and Modulating Aging Volume 1067 published May 2006
Ann. N.Y. Acad. Sci. 1067: 500–505 (2006). doi: 10.1196/annals.1354.072
Copyright © 2006 by the New York Academy of Sciences
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Articles by SØRENSEN, M. D.
Articles by KRISTENSEN, P.
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Articles by SØRENSEN, M. D.
Articles by KRISTENSEN, P.

Severe Acute Respiratory Syndrome (SARS)

Development of Diagnostics and Antivirals

MORTEN DRÆBY SØRENSENa, BRIAN SØRENSENa, REGINA GONZALEZ-DOSALa, CONNIE JENNING MELCHJORSENa, JENS WEIBELa, JING WANGb, CHEN WIE JUNb, YANG HUANMINGb AND PETER KRISTENSENa

a Department of Molecular Biology, University of Aarhus, Aarhus, Denmark
b Beijing Genomics Institute, Beijing, China

Key Words: SARS • phage display • antibodies • antiviral agents

Address for correspondence: Dr. Peter Kristensen, Department of Molecular Biology, University of Aarhus, Gustav Wieds Vej 10C, DK8000 Aarhus–C, Denmark. Voice: +45 8942 5032; fax: +45 8612 3178.  e-mail: pk{at}mb.au.dk

The previously unknown coronavirus that caused severe acute respiratory syndrome (SARS-CoV) affected more than 8,000 persons worldwide and was responsible for more than 700 deaths during the first outbreak in 2002–2003. For reasons unknown, the SARS virus is less severe and the clinical progression a great deal milder in children younger than 12 years of age. In contrast, the mortality rate can exceed 50% for persons at or above the age of 60. As part of the Sino-European Project on SARS Diagnostics and Antivirals (SEPSDA), an immune phage-display library is being created from convalescent patients in a phagemid system for the selection of single-chain fragment variables (scFv) antibodies recognizing the SARS-CoV.




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