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CD3bright signals on γδ T cells identify IL-17A-producing Vγ6Vδ1+ T cells.

Identifieur interne : 002E75 ( PubMed/Checkpoint ); précédent : 002E74; suivant : 002E76

CD3bright signals on γδ T cells identify IL-17A-producing Vγ6Vδ1+ T cells.

Auteurs : C. Paget [France] ; M T Chow [Australie] ; N A Gherardin [Australie] ; P A Beavis [Australie] ; A P Uldrich [Australie] ; H. Duret [Australie] ; M. Hassane [France] ; F. Souza-Fonseca-Guimaraes [Australie] ; D A Mogilenko [France] ; D. Staumont-Sallé [France] ; N K Escalante [Canada] ; G R Hill [Australie] ; P. Neeson [Australie] ; D S Ritchie [Australie] ; D. Dombrowicz [France] ; T. Mallevaey [Canada] ; F. Trottein [France] ; G T Belz [Australie] ; D I Godfrey [Australie] ; M J Smyth [Australie]

Source :

RBID : pubmed:25385067

Descripteurs français

English descriptors

Abstract

Interleukin-17A (IL-17A) is a pro-inflammatory cytokine that has an important role at mucosal sites in a wide range of immune responses including infection, allergy and auto-immunity. γδ T cells are recognized as IL-17 producers, but based on the level of CD3 expression, we now define the remarkable ability of a CD3(bright) γδ T-cell subset with an effector memory phenotype to rapidly produce IL-17A, but not interferon-γ. CD3(bright) γδ T cells uniformly express the canonical germline encoded Vγ6/Vδ1(+) T-cell receptor. They are widely distributed with a preferential representation in the lungs and skin are negatively impacted in the absence of retinoic acid receptor-related orphan receptor gammat expression or endogenous flora. This population responded rapidly to various stimuli in a mechanism involving IL-23 and NOD-like receptor family, pyrin domain containing 3 (NLRP3)-inflammasome-dependent IL-1β. Finally, we demonstrated that IL-17-producing CD3(bright) γδ T cells responded promptly and strongly to pneumococcal infection and during skin inflammation. Here, we propose a new way to specifically analyze IL-17-producing Vγ6/Vδ1(+) T cells based on the level of CD3 signals. Using this gating strategy, our data reinforce the crucial role of this γδ T-cell subset in respiratory and skin disorders.

DOI: 10.1038/icb.2014.94
PubMed: 25385067


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pubmed:25385067

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<nlm:affiliation>1] University of Lille 2, Lille, France [2] INSERM U1011, Institut Pasteur de Lille, Lille, France [3] European Genomic Institute of Diabetes, Lille, France [4] Department of Dermatology, Claude Huriez Hospital, Lille, France.</nlm:affiliation>
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<name sortKey="Neeson, P" sort="Neeson, P" uniqKey="Neeson P" first="P" last="Neeson">P. Neeson</name>
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<name sortKey="Dombrowicz, D" sort="Dombrowicz, D" uniqKey="Dombrowicz D" first="D" last="Dombrowicz">D. Dombrowicz</name>
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<nlm:affiliation>Department of Immunology, University of Toronto, Toronto, Ontario, Canada.</nlm:affiliation>
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<orgName type="university">Université de Toronto</orgName>
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<nlm:affiliation>Division of Molecular Immunology, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.</nlm:affiliation>
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<nlm:affiliation>1] Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, Australia [2] Australian Research Council Centre of Excellence in Advanced Medical Imaging at University of Melbourne, Parkville, Victoria, Australia.</nlm:affiliation>
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<nlm:affiliation>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.</nlm:affiliation>
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<wicri:regionArea>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] QIMR Berghofer Medical Research Institute, Herston, Queensland</wicri:regionArea>
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<nlm:affiliation>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, Australia.</nlm:affiliation>
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<country xml:lang="fr">Australie</country>
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<country xml:lang="fr">Australie</country>
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<name sortKey="Duret, H" sort="Duret, H" uniqKey="Duret H" first="H" last="Duret">H. Duret</name>
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<name sortKey="Hassane, M" sort="Hassane, M" uniqKey="Hassane M" first="M" last="Hassane">M. Hassane</name>
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<country xml:lang="fr">France</country>
<wicri:regionArea>1] INSERM U1019, Centre d'Infection et d'Immunité de Lille, Institut Pasteur de Lille, Lille, France [2] University of Lille 2, Lille</wicri:regionArea>
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<name sortKey="Souza Fonseca Guimaraes, F" sort="Souza Fonseca Guimaraes, F" uniqKey="Souza Fonseca Guimaraes F" first="F" last="Souza-Fonseca-Guimaraes">F. Souza-Fonseca-Guimaraes</name>
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<name sortKey="Mogilenko, D A" sort="Mogilenko, D A" uniqKey="Mogilenko D" first="D A" last="Mogilenko">D A Mogilenko</name>
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<nlm:affiliation>1] University of Lille 2, Lille, France [2] INSERM U1011, Institut Pasteur de Lille, Lille, France [3] European Genomic Institute of Diabetes, Lille, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
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<name sortKey="Staumont Salle, D" sort="Staumont Salle, D" uniqKey="Staumont Salle D" first="D" last="Staumont-Sallé">D. Staumont-Sallé</name>
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<nlm:affiliation>1] University of Lille 2, Lille, France [2] INSERM U1011, Institut Pasteur de Lille, Lille, France [3] European Genomic Institute of Diabetes, Lille, France [4] Department of Dermatology, Claude Huriez Hospital, Lille, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>1] University of Lille 2, Lille, France [2] INSERM U1011, Institut Pasteur de Lille, Lille, France [3] European Genomic Institute of Diabetes, Lille, France [4] Department of Dermatology, Claude Huriez Hospital, Lille</wicri:regionArea>
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<name sortKey="Escalante, N K" sort="Escalante, N K" uniqKey="Escalante N" first="N K" last="Escalante">N K Escalante</name>
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<nlm:affiliation>Department of Immunology, University of Toronto, Toronto, Ontario, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
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<orgName type="university">Université de Toronto</orgName>
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<region type="state">Ontario</region>
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<name sortKey="Hill, G R" sort="Hill, G R" uniqKey="Hill G" first="G R" last="Hill">G R Hill</name>
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<nlm:affiliation>1] QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia [2] Department of Bone Marrow Transplantation, Royal Brisbane Hospital, Herston, Queensland, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>1] QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia [2] Department of Bone Marrow Transplantation, Royal Brisbane Hospital, Herston, Queensland</wicri:regionArea>
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<name sortKey="Neeson, P" sort="Neeson, P" uniqKey="Neeson P" first="P" last="Neeson">P. Neeson</name>
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<country xml:lang="fr">Australie</country>
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<settlement type="city">Melbourne</settlement>
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<nlm:affiliation>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria</wicri:regionArea>
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<settlement type="city">Melbourne</settlement>
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<name sortKey="Dombrowicz, D" sort="Dombrowicz, D" uniqKey="Dombrowicz D" first="D" last="Dombrowicz">D. Dombrowicz</name>
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<nlm:affiliation>1] University of Lille 2, Lille, France [2] INSERM U1011, Institut Pasteur de Lille, Lille, France [3] European Genomic Institute of Diabetes, Lille, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>1] University of Lille 2, Lille, France [2] INSERM U1011, Institut Pasteur de Lille, Lille, France [3] European Genomic Institute of Diabetes, Lille</wicri:regionArea>
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<region type="region">Hauts-de-France</region>
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<settlement type="city">Lille</settlement>
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<name sortKey="Mallevaey, T" sort="Mallevaey, T" uniqKey="Mallevaey T" first="T" last="Mallevaey">T. Mallevaey</name>
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<nlm:affiliation>Department of Immunology, University of Toronto, Toronto, Ontario, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Immunology, University of Toronto, Toronto, Ontario</wicri:regionArea>
<orgName type="university">Université de Toronto</orgName>
<placeName>
<settlement type="city">Toronto</settlement>
<region type="state">Ontario</region>
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<name sortKey="Trottein, F" sort="Trottein, F" uniqKey="Trottein F" first="F" last="Trottein">F. Trottein</name>
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<nlm:affiliation>1] INSERM U1019, Centre d'Infection et d'Immunité de Lille, Institut Pasteur de Lille, Lille, France [2] University of Lille 2, Lille, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>1] INSERM U1019, Centre d'Infection et d'Immunité de Lille, Institut Pasteur de Lille, Lille, France [2] University of Lille 2, Lille</wicri:regionArea>
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<name sortKey="Belz, G T" sort="Belz, G T" uniqKey="Belz G" first="G T" last="Belz">G T Belz</name>
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<nlm:affiliation>Division of Molecular Immunology, Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
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<name sortKey="Godfrey, D I" sort="Godfrey, D I" uniqKey="Godfrey D" first="D I" last="Godfrey">D I Godfrey</name>
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<nlm:affiliation>1] Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, Australia [2] Australian Research Council Centre of Excellence in Advanced Medical Imaging at University of Melbourne, Parkville, Victoria, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>1] Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, Australia [2] Australian Research Council Centre of Excellence in Advanced Medical Imaging at University of Melbourne, Parkville, Victoria</wicri:regionArea>
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<settlement type="city">Melbourne</settlement>
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<name sortKey="Smyth, M J" sort="Smyth, M J" uniqKey="Smyth M" first="M J" last="Smyth">M J Smyth</name>
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<nlm:affiliation>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia [4] School of Medicine, University of Queensland, Herston, Queensland, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia [4] School of Medicine, University of Queensland, Herston, Queensland</wicri:regionArea>
<orgName type="university">Université de Melbourne</orgName>
<placeName>
<settlement type="city">Melbourne</settlement>
<region type="état">Victoria (État)</region>
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<term>Amino Acid Sequence</term>
<term>Aminoquinolines (pharmacology)</term>
<term>Animals</term>
<term>Antigens, CD3 (chemistry)</term>
<term>Antigens, CD3 (metabolism)</term>
<term>Carrier Proteins (metabolism)</term>
<term>Germ Cells (drug effects)</term>
<term>Homeostasis (drug effects)</term>
<term>Immunity</term>
<term>Inflammasomes (drug effects)</term>
<term>Inflammasomes (metabolism)</term>
<term>Interleukin-17 (biosynthesis)</term>
<term>Interleukin-1beta (metabolism)</term>
<term>Interleukin-23</term>
<term>Lung (drug effects)</term>
<term>Lung (immunology)</term>
<term>Lymphocyte Subsets (drug effects)</term>
<term>Lymphocyte Subsets (immunology)</term>
<term>Male</term>
<term>Mice, Inbred C57BL</term>
<term>Molecular Sequence Data</term>
<term>NLR Family, Pyrin Domain-Containing 3 Protein</term>
<term>Nuclear Receptor Subfamily 1, Group F, Member 3 (metabolism)</term>
<term>Phenotype</term>
<term>Receptors, Antigen, T-Cell, gamma-delta (metabolism)</term>
<term>Skin (drug effects)</term>
<term>Skin (immunology)</term>
<term>T-Lymphocytes (drug effects)</term>
<term>T-Lymphocytes (immunology)</term>
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<term>Antigènes CD3 (métabolisme)</term>
<term>Cellules germinales ()</term>
<term>Données de séquences moléculaires</term>
<term>Homéostasie ()</term>
<term>Immunité</term>
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<term>Inflammasomes (métabolisme)</term>
<term>Interleukine-1 bêta (métabolisme)</term>
<term>Interleukine-17 (biosynthèse)</term>
<term>Interleukine-23</term>
<term>Lymphocytes T ()</term>
<term>Lymphocytes T (immunologie)</term>
<term>Membre-3 du groupe F de la sous-famille-1 de récepteurs nucléaires (métabolisme)</term>
<term>Mâle</term>
<term>Peau ()</term>
<term>Peau (immunologie)</term>
<term>Phénotype</term>
<term>Poumon ()</term>
<term>Poumon (immunologie)</term>
<term>Protéine-3 de la famille des NLR contenant un domaine pyrine</term>
<term>Protéines de transport (métabolisme)</term>
<term>Récepteur lymphocytaire T antigène, gamma-delta (métabolisme)</term>
<term>Souris de lignée C57BL</term>
<term>Sous-populations de lymphocytes ()</term>
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<term>Séquence d'acides aminés</term>
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<term>Skin</term>
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<term>Lymphocytes T</term>
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<term>Poumon</term>
<term>Sous-populations de lymphocytes</term>
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<term>Lymphocyte Subsets</term>
<term>Skin</term>
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<term>Antigènes CD3</term>
<term>Inflammasomes</term>
<term>Interleukine-1 bêta</term>
<term>Membre-3 du groupe F de la sous-famille-1 de récepteurs nucléaires</term>
<term>Protéines de transport</term>
<term>Récepteur lymphocytaire T antigène, gamma-delta</term>
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<term>Aminoquinoléines</term>
</keywords>
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<term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Immunity</term>
<term>Interleukin-23</term>
<term>Male</term>
<term>Mice, Inbred C57BL</term>
<term>Molecular Sequence Data</term>
<term>NLR Family, Pyrin Domain-Containing 3 Protein</term>
<term>Phenotype</term>
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<term>Animaux</term>
<term>Antigènes CD3</term>
<term>Cellules germinales</term>
<term>Données de séquences moléculaires</term>
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<div type="abstract" xml:lang="en">Interleukin-17A (IL-17A) is a pro-inflammatory cytokine that has an important role at mucosal sites in a wide range of immune responses including infection, allergy and auto-immunity. γδ T cells are recognized as IL-17 producers, but based on the level of CD3 expression, we now define the remarkable ability of a CD3(bright) γδ T-cell subset with an effector memory phenotype to rapidly produce IL-17A, but not interferon-γ. CD3(bright) γδ T cells uniformly express the canonical germline encoded Vγ6/Vδ1(+) T-cell receptor. They are widely distributed with a preferential representation in the lungs and skin are negatively impacted in the absence of retinoic acid receptor-related orphan receptor gammat expression or endogenous flora. This population responded rapidly to various stimuli in a mechanism involving IL-23 and NOD-like receptor family, pyrin domain containing 3 (NLRP3)-inflammasome-dependent IL-1β. Finally, we demonstrated that IL-17-producing CD3(bright) γδ T cells responded promptly and strongly to pneumococcal infection and during skin inflammation. Here, we propose a new way to specifically analyze IL-17-producing Vγ6/Vδ1(+) T cells based on the level of CD3 signals. Using this gating strategy, our data reinforce the crucial role of this γδ T-cell subset in respiratory and skin disorders.</div>
</front>
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<DateCreated>
<Year>2015</Year>
<Month>02</Month>
<Day>10</Day>
</DateCreated>
<DateCompleted>
<Year>2015</Year>
<Month>12</Month>
<Day>14</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>11</Month>
<Day>16</Day>
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<Issue>2</Issue>
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<Year>2015</Year>
<Month>Feb</Month>
</PubDate>
</JournalIssue>
<Title>Immunology and cell biology</Title>
<ISOAbbreviation>Immunol. Cell Biol.</ISOAbbreviation>
</Journal>
<ArticleTitle>CD3bright signals on γδ T cells identify IL-17A-producing Vγ6Vδ1+ T cells.</ArticleTitle>
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<MedlinePgn>198-212</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1038/icb.2014.94</ELocationID>
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<AbstractText>Interleukin-17A (IL-17A) is a pro-inflammatory cytokine that has an important role at mucosal sites in a wide range of immune responses including infection, allergy and auto-immunity. γδ T cells are recognized as IL-17 producers, but based on the level of CD3 expression, we now define the remarkable ability of a CD3(bright) γδ T-cell subset with an effector memory phenotype to rapidly produce IL-17A, but not interferon-γ. CD3(bright) γδ T cells uniformly express the canonical germline encoded Vγ6/Vδ1(+) T-cell receptor. They are widely distributed with a preferential representation in the lungs and skin are negatively impacted in the absence of retinoic acid receptor-related orphan receptor gammat expression or endogenous flora. This population responded rapidly to various stimuli in a mechanism involving IL-23 and NOD-like receptor family, pyrin domain containing 3 (NLRP3)-inflammasome-dependent IL-1β. Finally, we demonstrated that IL-17-producing CD3(bright) γδ T cells responded promptly and strongly to pneumococcal infection and during skin inflammation. Here, we propose a new way to specifically analyze IL-17-producing Vγ6/Vδ1(+) T cells based on the level of CD3 signals. Using this gating strategy, our data reinforce the crucial role of this γδ T-cell subset in respiratory and skin disorders.</AbstractText>
</Abstract>
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<Author ValidYN="Y">
<LastName>Paget</LastName>
<ForeName>C</ForeName>
<Initials>C</Initials>
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<Affiliation>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] INSERM U1019, Centre d'Infection et d'Immunité de Lille, Institut Pasteur de Lille, Lille, France [4] University of Lille 2, Lille, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Chow</LastName>
<ForeName>M T</ForeName>
<Initials>MT</Initials>
<AffiliationInfo>
<Affiliation>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] QIMR Berghofer Medical Research Institute, Herston, Queensland, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gherardin</LastName>
<ForeName>N A</ForeName>
<Initials>NA</Initials>
<AffiliationInfo>
<Affiliation>1] Peter MacCallum Cancer Centre, Cancer Immunology Program, St Andrews Place, East Melbourne, Victoria, Australia [2] Sir Peter MacCallum Department of Oncology and Department of Pathology, University of Melbourne, Parkville, Victoria, Australia [3] Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Victoria, Australia.</Affiliation>
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<name sortKey="Smyth, M J" sort="Smyth, M J" uniqKey="Smyth M" first="M J" last="Smyth">M J Smyth</name>
<name sortKey="Souza Fonseca Guimaraes, F" sort="Souza Fonseca Guimaraes, F" uniqKey="Souza Fonseca Guimaraes F" first="F" last="Souza-Fonseca-Guimaraes">F. Souza-Fonseca-Guimaraes</name>
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