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Human CD4+ memory T-lymphocyte responses to SARS coronavirus infection

Identifieur interne : 003829 ( Main/Merge ); précédent : 003828; suivant : 003830

Human CD4+ memory T-lymphocyte responses to SARS coronavirus infection

Auteurs : Daniel H. Libraty [États-Unis] ; Kimberly M. O'Neil [États-Unis] ; Lauren M. Baker [États-Unis] ; Luz P. Acosta [Philippines] ; Remigio M. Olveda [Philippines]

Source :

RBID : PMC:2094716

Descripteurs français

English descriptors

Abstract

Little is known about CD4+ T-cell immunity to the severe acute respiratory syndrome (SARS) coronavirus. In two SARS patients, we examined the memory CD4+ T-cell responses to peptides derived from SARS coronavirus structural proteins. We generated CD4+ T-cell lines to 3 peptides from the spike (S) protein and defined their HLA restriction. In one patient, the predominant memory CD4+ T-cell response was directed against an epitope outside the S protein receptor-binding domain. In both patients, the frequency of CD4+ memory T-cells to virus structural proteins and anti-SARS coronavirus IgG levels were low by 12 months after infection. This report expands our understanding of the specificity and duration of anti-SARS coronavirus CD4+ T-cell immune responses.


Url:
DOI: 10.1016/j.virol.2007.07.015
PubMed: 17692881
PubMed Central: 2094716

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PMC:2094716

Le document en format XML

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memory T-lymphocyte responses to SARS coronavirus infection</title>
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<term>Humans</term>
<term>Immunologic Memory (immunology)</term>
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<div type="abstract" xml:lang="en">
<p>Little is known about CD4
<sup>+</sup>
T-cell immunity to the severe acute respiratory syndrome (SARS) coronavirus. In two SARS patients, we examined the memory CD4
<sup>+</sup>
T-cell responses to peptides derived from SARS coronavirus structural proteins. We generated CD4
<sup>+</sup>
T-cell lines to 3 peptides from the spike (S) protein and defined their HLA restriction. In one patient, the predominant memory CD4
<sup>+</sup>
T-cell response was directed against an epitope outside the S protein receptor-binding domain. In both patients, the frequency of CD4
<sup>+</sup>
memory T-cells to virus structural proteins and anti-SARS coronavirus IgG levels were low by 12 months after infection. This report expands our understanding of the specificity and duration of anti-SARS coronavirus CD4
<sup>+</sup>
T-cell immune responses.</p>
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<div1 type="bibliography">
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