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Antibody avidity maturation during severe acute respiratory syndrome-associated coronavirus infection.

Identifieur interne : 000F98 ( Ncbi/Checkpoint ); précédent : 000F97; suivant : 000F99

Antibody avidity maturation during severe acute respiratory syndrome-associated coronavirus infection.

Auteurs : Paul K S. Chan [République populaire de Chine] ; Pak-Leong Lim ; Esther Y M. Liu ; Jo L K. Cheung ; Danny T M. Leung ; Joseph J Y. Sung

Source :

RBID : pubmed:15942907

Descripteurs français

English descriptors

Abstract

The maturation of virus-specific immunoglobulin G avidity during severe acute respiratory syndrome-associated coronavirus infection was examined. The avidity indices were low (mean +/- SD, 30.8% +/- 11.6%) among serum samples collected < or =50 days after fever onset, intermediate (mean +/- SD, 52.1% +/- 14.1%) among samples collected between days 51 and 90, and high (mean +/- SD, 78.1% +/- 8.0%) among samples collected after day 90. Avidity indices of 40% and 55% could be considered as cutoff values for determination of recent (< or =50 days) and past (>65 days) infection, respectively. Measurement of antibody avidity can be used to differentiate primary infection from reexposure and to assess humoral responses to candidate vaccines.

DOI: 10.1086/430615
PubMed: 15942907


Affiliations:


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pubmed:15942907

Le document en format XML

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<front>
<div type="abstract" xml:lang="en">The maturation of virus-specific immunoglobulin G avidity during severe acute respiratory syndrome-associated coronavirus infection was examined. The avidity indices were low (mean +/- SD, 30.8% +/- 11.6%) among serum samples collected < or =50 days after fever onset, intermediate (mean +/- SD, 52.1% +/- 14.1%) among samples collected between days 51 and 90, and high (mean +/- SD, 78.1% +/- 8.0%) among samples collected after day 90. Avidity indices of 40% and 55% could be considered as cutoff values for determination of recent (< or =50 days) and past (>65 days) infection, respectively. Measurement of antibody avidity can be used to differentiate primary infection from reexposure and to assess humoral responses to candidate vaccines.</div>
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