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Evaluation of a recombinant nucleocapsid protein-based assay for anti-SARS-CoV IgG detection

Identifieur interne : 000656 ( PascalFrancis/Checkpoint ); précédent : 000655; suivant : 000657

Evaluation of a recombinant nucleocapsid protein-based assay for anti-SARS-CoV IgG detection

Auteurs : Paul K. S. Chan [Hong Kong] ; Esther Y. M. Liu [Hong Kong] ; Danny T. M. Leung [Hong Kong] ; Jo L. K. Cheung [Hong Kong] ; C. H. Ma [Hong Kong] ; Frankie C. H. Tam [Hong Kong] ; Mamie Hui [Hong Kong] ; John S. Tam [Hong Kong] ; PAK LEONG LIM [Hong Kong]

Source :

RBID : Pascal:05-0458730

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English descriptors

Abstract

A high throughput accurate assay for anti-SARS-CoV IgG detection is needed for large-scale epidemiological studies. The evaluation of a commercial recombinant nucleocapsid protein-based microtitre plate enzyme immunoassay, ELISARS is described. The results on 150 sera from SARS patients and 450 sera from non-SARS controls showed that this assay had a high level of sensitivity (96.2% for late serum samples) and specificity (97.8%). The performance and setup of this assay fulfills the requirement as a screening test for large-scale studies. A vast majority of SARS patients developed antibodies against the nucleocapsid protein. In some patients (10/45), a high level of anti-nucleocapsid antibody appeared very early in the course of the illness. In contrast, a minority (4 of 105 patients) never developed these antibodies. The implication of differences in antibody response to the nucleocapsid protein deserves further investigation.


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Pascal:05-0458730

Le document en format XML

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<div type="abstract" xml:lang="en">A high throughput accurate assay for anti-SARS-CoV IgG detection is needed for large-scale epidemiological studies. The evaluation of a commercial recombinant nucleocapsid protein-based microtitre plate enzyme immunoassay, ELISARS is described. The results on 150 sera from SARS patients and 450 sera from non-SARS controls showed that this assay had a high level of sensitivity (96.2% for late serum samples) and specificity (97.8%). The performance and setup of this assay fulfills the requirement as a screening test for large-scale studies. A vast majority of SARS patients developed antibodies against the nucleocapsid protein. In some patients (10/45), a high level of anti-nucleocapsid antibody appeared very early in the course of the illness. In contrast, a minority (4 of 105 patients) never developed these antibodies. The implication of differences in antibody response to the nucleocapsid protein deserves further investigation.</div>
</front>
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<s1>CHEUNG (Jo L. K.)</s1>
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<s1>MA (C. H.)</s1>
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<s1>TAM (John S.)</s1>
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<s1>PAK LEONG LIM</s1>
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<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>7 aut.</sZ>
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<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
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<s1>© 2005 INIST-CNRS. All rights reserved.</s1>
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<fA45>
<s0>24 ref.</s0>
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<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>A high throughput accurate assay for anti-SARS-CoV IgG detection is needed for large-scale epidemiological studies. The evaluation of a commercial recombinant nucleocapsid protein-based microtitre plate enzyme immunoassay, ELISARS is described. The results on 150 sera from SARS patients and 450 sera from non-SARS controls showed that this assay had a high level of sensitivity (96.2% for late serum samples) and specificity (97.8%). The performance and setup of this assay fulfills the requirement as a screening test for large-scale studies. A vast majority of SARS patients developed antibodies against the nucleocapsid protein. In some patients (10/45), a high level of anti-nucleocapsid antibody appeared very early in the course of the illness. In contrast, a minority (4 of 105 patients) never developed these antibodies. The implication of differences in antibody response to the nucleocapsid protein deserves further investigation.</s0>
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<s0>002A05C08</s0>
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<s0>Coronavirus</s0>
<s2>NW</s2>
<s5>01</s5>
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<s5>05</s5>
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<fC03 i1="03" i2="X" l="SPA">
<s0>Nucleocápside</s0>
<s5>06</s5>
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<fC03 i1="04" i2="X" l="FRE">
<s0>IgG</s0>
<s5>07</s5>
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<s5>07</s5>
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<s5>14</s5>
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<s0>Severe acute respiratory syndrome</s0>
<s2>NM</s2>
<s5>14</s5>
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<fC03 i1="10" i2="X" l="SPA">
<s0>Síndrome respiratorio agudo severo</s0>
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<s5>14</s5>
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<s0>Coronaviridae</s0>
<s2>NW</s2>
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<s0>Coronaviridae</s0>
<s2>NW</s2>
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<s2>NW</s2>
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<s0>Nidovirales</s0>
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<s0>Virus</s0>
<s2>NW</s2>
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<s0>Virus</s0>
<s2>NW</s2>
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<fC07 i1="03" i2="X" l="SPA">
<s0>Virus</s0>
<s2>NW</s2>
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<s5>16</s5>
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<fN21>
<s1>325</s1>
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<fN44 i1="01">
<s1>OTO</s1>
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<fN82>
<s1>OTO</s1>
</fN82>
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<affiliations>
<list>
<country>
<li>Hong Kong</li>
</country>
<settlement>
<li>Sha Tin</li>
</settlement>
<orgName>
<li>Université chinoise de Hong Kong</li>
</orgName>
</list>
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<name sortKey="Chan, Paul K S" sort="Chan, Paul K S" uniqKey="Chan P" first="Paul K. S." last="Chan">Paul K. S. Chan</name>
</noRegion>
<name sortKey="Chan, Paul K S" sort="Chan, Paul K S" uniqKey="Chan P" first="Paul K. S." last="Chan">Paul K. S. Chan</name>
<name sortKey="Cheung, Jo L K" sort="Cheung, Jo L K" uniqKey="Cheung J" first="Jo L. K." last="Cheung">Jo L. K. Cheung</name>
<name sortKey="Hui, Mamie" sort="Hui, Mamie" uniqKey="Hui M" first="Mamie" last="Hui">Mamie Hui</name>
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<name sortKey="Liu, Esther Y M" sort="Liu, Esther Y M" uniqKey="Liu E" first="Esther Y. M." last="Liu">Esther Y. M. Liu</name>
<name sortKey="Ma, C H" sort="Ma, C H" uniqKey="Ma C" first="C. H." last="Ma">C. H. Ma</name>
<name sortKey="Pak Leong Lim" sort="Pak Leong Lim" uniqKey="Pak Leong Lim" last="Pak Leong Lim">PAK LEONG LIM</name>
<name sortKey="Tam, Frankie C H" sort="Tam, Frankie C H" uniqKey="Tam F" first="Frankie C. H." last="Tam">Frankie C. H. Tam</name>
<name sortKey="Tam, John S" sort="Tam, John S" uniqKey="Tam J" first="John S." last="Tam">John S. Tam</name>
<name sortKey="Tam, John S" sort="Tam, John S" uniqKey="Tam J" first="John S." last="Tam">John S. Tam</name>
</country>
</tree>
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</record>

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