Anti-severe acute respiratory syndrome coronavirus immune responses : The role played by Vγ9Vδ2 T cells
Identifieur interne : 004709 ( Main/Merge ); précédent : 004708; suivant : 004710Anti-severe acute respiratory syndrome coronavirus immune responses : The role played by Vγ9Vδ2 T cells
Auteurs : Fabrizio Poccia [Italie] ; Chiara Agrati [Italie] ; Concetta Castilletti [Italie] ; Licia Bordi [Italie] ; Cristiana Gioia [Italie] ; Douglas Horejsh [Italie] ; Giuseppe Ippolito [Italie] ; Paul K. S. Chan [Hong Kong] ; David S. C. Hui [Hong Kong] ; Joseph J. Y. Sung [Hong Kong] ; Maria Rosaria Capobianchi [Italie] ; Miroslav Malkovsky [États-Unis]Source :
- The Journal of infectious diseases [ 0022-1899 ] ; 2006.
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- Pascal (Inist)
English descriptors
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Abstract
Severe acute respiratory syndrome (SARS) is caused by a novel coronavirus (SARS-CoV) strain. Analyses ofT cell repertoires in health care workers who survived SARS-CoV infection during the 2003 outbreak revealed that their effector memory Vγ9Vδ2 T cell populations were selectively expanded ∼3 months after the onset of disease. No such expansion of their αβ T cell pools was detected. The expansion of the Vγ9Vδ2 T cell population was associated with higher anti-SARS-CoV immunoglobulin G titers. In addition, in vitro experiments demonstrated that stimulated Vγ9Vδ2 T cells display an interferon-γ-dependent anti-SARS-CoV activity and are able to directly kill SARS-CoV-infected target cells. These findings are compatible with the possibility that Vγ9Vδ2 T cells play a protective role during SARS.
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<series><title level="j" type="main">The Journal of infectious diseases</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Coronavirus</term>
<term>Immune response</term>
<term>Infection</term>
<term>Microbiology</term>
<term>Severe acute respiratory syndrome</term>
<term>T-Lymphocyte</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Coronavirus</term>
<term>Réponse immune</term>
<term>Lymphocyte T</term>
<term>Microbiologie</term>
<term>Infection</term>
<term>Syndrome respiratoire aigu sévère</term>
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is caused by a novel coronavirus (SARS-CoV) strain. Analyses ofT cell repertoires in health care workers who survived SARS-CoV infection during the 2003 outbreak revealed that their effector memory Vγ9Vδ2 T cell populations were selectively expanded ∼3 months after the onset of disease. No such expansion of their αβ T cell pools was detected. The expansion of the Vγ9Vδ2 T cell population was associated with higher anti-SARS-CoV immunoglobulin G titers. In addition, in vitro experiments demonstrated that stimulated Vγ9Vδ2 T cells display an interferon-γ-dependent anti-SARS-CoV activity and are able to directly kill SARS-CoV-infected target cells. These findings are compatible with the possibility that Vγ9Vδ2 T cells play a protective role during SARS.</div>
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<country name="États-Unis"><noRegion><name sortKey="Malkovsky, Miroslav" sort="Malkovsky, Miroslav" uniqKey="Malkovsky M" first="Miroslav" last="Malkovsky">Miroslav Malkovsky</name>
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