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Anti–Severe Acute Respiratory Syndrome Coronavirus Immune Responses: The Role Played by Vγ9Vδ2 T Cells

Identifieur interne : 001443 ( Ncbi/Merge ); précédent : 001442; suivant : 001444

Anti–Severe Acute Respiratory Syndrome Coronavirus Immune Responses: The Role Played by Vγ9Vδ2 T Cells

Auteurs : Fabrizio Poccia ; Chiara Agrati ; Concetta Castilletti ; Licia Bordi ; Cristiana Gioia ; Douglas Horejsh ; Giuseppe Ippolito [Italie] ; Paul K. S. Chan [République populaire de Chine] ; David S. C. Hui [République populaire de Chine] ; Joseph J. Y. Sung [République populaire de Chine] ; Maria Rosaria Capobianchi ; Miroslav Malkovsky

Source :

RBID : PMC:7110256

Descripteurs français

English descriptors

Abstract

Abstract

Severe acute respiratory syndrome (SARS) is caused by a novel coronavirus (SARS-CoV) strain. Analyses of T 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


Url:
DOI: 10.1086/502975
PubMed: 16586361
PubMed Central: 7110256

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PMC:7110256

Le document en format XML

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<name sortKey="Capobianchi, Maria Rosaria" sort="Capobianchi, Maria Rosaria" uniqKey="Capobianchi M" first="Maria Rosaria" last="Capobianchi">Maria Rosaria Capobianchi</name>
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<name sortKey="Malkovsky, Miroslav" sort="Malkovsky, Miroslav" uniqKey="Malkovsky M" first="Miroslav" last="Malkovsky">Miroslav Malkovsky</name>
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<title level="j">The Journal of Infectious Diseases</title>
<idno type="ISSN">0022-1899</idno>
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<title>Abstract</title>
<p>Severe acute respiratory syndrome (SARS) is caused by a novel coronavirus (SARS-CoV) strain. Analyses of T 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</p>
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<name sortKey="Poccia, Fabrizio" sort="Poccia, Fabrizio" uniqKey="Poccia F" first="Fabrizio" last="Poccia">Fabrizio Poccia</name>
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<name sortKey="Poccia, Fabrizio" sort="Poccia, Fabrizio" uniqKey="Poccia F" first="Fabrizio" last="Poccia">Fabrizio Poccia</name>
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<nlm:affiliation>Unit of Cellular Immunology, National Institute for Infectious Diseases Lazzaro Spallanzani, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy. poccia@inmi.it</nlm:affiliation>
<country xml:lang="fr">Italie</country>
<wicri:regionArea>Unit of Cellular Immunology, National Institute for Infectious Diseases Lazzaro Spallanzani, Istituto di Ricovero e Cura a Carattere Scientifico, Rome</wicri:regionArea>
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<region nuts="2">Latium</region>
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<name sortKey="Agrati, Chiara" sort="Agrati, Chiara" uniqKey="Agrati C" first="Chiara" last="Agrati">Chiara Agrati</name>
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<name sortKey="Castilletti, Concetta" sort="Castilletti, Concetta" uniqKey="Castilletti C" first="Concetta" last="Castilletti">Concetta Castilletti</name>
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<name sortKey="Bordi, Licia" sort="Bordi, Licia" uniqKey="Bordi L" first="Licia" last="Bordi">Licia Bordi</name>
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<name sortKey="Gioia, Cristiana" sort="Gioia, Cristiana" uniqKey="Gioia C" first="Cristiana" last="Gioia">Cristiana Gioia</name>
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<name sortKey="Sung, Joseph J Y" sort="Sung, Joseph J Y" uniqKey="Sung J" first="Joseph J Y" last="Sung">Joseph J Y. Sung</name>
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<name sortKey="Capobianchi, Maria Rosaria" sort="Capobianchi, Maria Rosaria" uniqKey="Capobianchi M" first="Maria Rosaria" last="Capobianchi">Maria Rosaria Capobianchi</name>
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<name sortKey="Malkovsky, Miroslav" sort="Malkovsky, Miroslav" uniqKey="Malkovsky M" first="Miroslav" last="Malkovsky">Miroslav Malkovsky</name>
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<title level="j">The Journal of infectious diseases</title>
<idno type="ISSN">0022-1899</idno>
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<term>Adult</term>
<term>Antibodies, Viral (blood)</term>
<term>Female</term>
<term>Humans</term>
<term>Immunoglobulin G (blood)</term>
<term>Immunologic Memory</term>
<term>Male</term>
<term>Receptors, Antigen, T-Cell, gamma-delta (analysis)</term>
<term>SARS Virus (immunology)</term>
<term>Severe Acute Respiratory Syndrome (immunology)</term>
<term>T-Lymphocyte Subsets (immunology)</term>
</keywords>
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<term>Adulte</term>
<term>Anticorps antiviraux (sang)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Immunoglobuline G (sang)</term>
<term>Mâle</term>
<term>Mémoire immunologique</term>
<term>Récepteur lymphocytaire T antigène, gamma-delta (analyse)</term>
<term>Sous-populations de lymphocytes T (immunologie)</term>
<term>Syndrome respiratoire aigu sévère (immunologie)</term>
<term>Virus du SRAS (immunologie)</term>
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<term>Receptors, Antigen, T-Cell, gamma-delta</term>
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<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en">
<term>Antibodies, Viral</term>
<term>Immunoglobulin G</term>
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<term>Récepteur lymphocytaire T antigène, gamma-delta</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Sous-populations de lymphocytes T</term>
<term>Syndrome respiratoire aigu sévère</term>
<term>Virus du SRAS</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>SARS Virus</term>
<term>Severe Acute Respiratory Syndrome</term>
<term>T-Lymphocyte Subsets</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr">
<term>Anticorps antiviraux</term>
<term>Immunoglobuline G</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Female</term>
<term>Humans</term>
<term>Immunologic Memory</term>
<term>Male</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
<term>Mémoire immunologique</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 of T cell repertoires in health care workers who survived SARS-CoV infection during the 2003 outbreak revealed that their effector memory V gamma 9V delta 2 T cell populations were selectively expanded ~3 months after the onset of disease. No such expansion of their alpha beta T cell pools was detected. The expansion of the V gamma 9V delta 2 T cell population was associated with higher anti-SARS-CoV immunoglobulin G titers. In addition, in vitro experiments demonstrated that stimulated V gamma 9V delta 2 T cells display an interferon- gamma -dependent anti-SARS-CoV activity and are able to directly kill SARS-CoV-infected target cells. These findings are compatible with the possibility that V gamma 9V delta 2 T cells play a protective role during SARS.</div>
</front>
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