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STAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and function

Identifieur interne : 002854 ( Main/Merge ); précédent : 002853; suivant : 002855

STAT3 is a critical cell-intrinsic regulator of human unconventional T cell numbers and function

Auteurs : Robert P. Wilson ; Megan L. Ives ; Geetha Rao ; Anthony Lau ; Kathryn Payne ; Masao Kobayashi ; Peter D. Arkwright ; Jane Peake ; Melanie Wong ; Stephen Adelstein ; Joanne M. Smart ; Martyn A. French ; David A. Fulcher ; Capucine Picard ; Jacinta Bustamante ; Stephanie Boisson-Dupuis ; Paul Gray ; Polina Stepensky ; Klaus Warnatz ; Alexandra F. Freeman ; Jamie Rossjohn ; James Mccluskey ; Steven M. Holland ; Jean-Laurent Casanova ; Gulbu Uzel ; Cindy S. Ma ; Stuart G. Tangye ; Elissa K. Deenick

Source :

RBID : PMC:4451129

Descripteurs français

English descriptors

Abstract

Wilson et al. show that individuals with loss-of-function mutations in STAT3 have reduced numbers of peripheral blood MAIT and NKT cells, but not γδ T cells. Residual MAIT cells had normal expression of RORγt, but displayed impaired secretion of IL-17A and IL-17F.


Url:
DOI: 10.1084/jem.20141992
PubMed: 25941256
PubMed Central: 4451129

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PMC:4451129

Le document en format XML

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<institution>Imagine Institute, Paris Descartes University, 75015 Paris, France</institution>
</nlm:aff>
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<affiliation>
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</affiliation>
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<institution>School of Women’s and Children’s Health, University of New South Wales, Sydney, NSW 2052, Australia</institution>
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<nlm:aff id="aff17">
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<institution>Imagine Institute, Paris Descartes University, 75015 Paris, France</institution>
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<institution>St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065</institution>
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<institution>St. Vincent’s Clinical School</institution>
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<institution>Immunology Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW 2010, Australia</institution>
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<affiliation>
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<institution>St. Vincent’s Clinical School</institution>
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</analytic>
<series>
<title level="j">The Journal of Experimental Medicine</title>
<idno type="ISSN">0022-1007</idno>
<idno type="eISSN">1540-9538</idno>
<imprint>
<date when="2015">2015</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Cell Separation</term>
<term>Cytokines (metabolism)</term>
<term>Flow Cytometry</term>
<term>Humans</term>
<term>Interferon-gamma (metabolism)</term>
<term>Interleukin-17 (metabolism)</term>
<term>Interleukin-23 (metabolism)</term>
<term>Interleukins (metabolism)</term>
<term>Killer Cells, Natural (cytology)</term>
<term>Leukocytes, Mononuclear (cytology)</term>
<term>Lymphocytes (cytology)</term>
<term>Mutation</term>
<term>Nuclear Receptor Subfamily 1, Group F, Member 3 (metabolism)</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Receptors, Antigen, T-Cell, gamma-delta (metabolism)</term>
<term>Receptors, Interleukin (metabolism)</term>
<term>Receptors, Interleukin-12 (metabolism)</term>
<term>Receptors, Interleukin-21 (metabolism)</term>
<term>STAT3 Transcription Factor (metabolism)</term>
<term>Signal Transduction</term>
<term>T-Lymphocytes (cytology)</term>
<term>Tumor Necrosis Factor-alpha (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Agranulocytes (cytologie)</term>
<term>Cellules tueuses naturelles (cytologie)</term>
<term>Cytokines (métabolisme)</term>
<term>Cytométrie en flux</term>
<term>Facteur de nécrose tumorale alpha (métabolisme)</term>
<term>Facteur de transcription STAT-3 (métabolisme)</term>
<term>Humains</term>
<term>Interféron gamma (métabolisme)</term>
<term>Interleukine-17 (métabolisme)</term>
<term>Interleukine-23 (métabolisme)</term>
<term>Interleukines (métabolisme)</term>
<term>Lymphocytes (cytologie)</term>
<term>Lymphocytes T (cytologie)</term>
<term>Membre-3 du groupe F de la sous-famille-1 de récepteurs nucléaires (métabolisme)</term>
<term>Mutation</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Récepteur lymphocytaire T antigène, gamma-delta (métabolisme)</term>
<term>Récepteurs aux interleukines (métabolisme)</term>
<term>Récepteurs à l'interleukine-12 (métabolisme)</term>
<term>Récepteurs à l'interleukine-21 (métabolisme)</term>
<term>Séparation cellulaire</term>
<term>Transduction du signal</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Cytokines</term>
<term>Interferon-gamma</term>
<term>Interleukin-17</term>
<term>Interleukin-23</term>
<term>Interleukins</term>
<term>Nuclear Receptor Subfamily 1, Group F, Member 3</term>
<term>Receptors, Antigen, T-Cell, gamma-delta</term>
<term>Receptors, Interleukin</term>
<term>Receptors, Interleukin-12</term>
<term>Receptors, Interleukin-21</term>
<term>STAT3 Transcription Factor</term>
<term>Tumor Necrosis Factor-alpha</term>
</keywords>
<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr">
<term>Agranulocytes</term>
<term>Cellules tueuses naturelles</term>
<term>Lymphocytes</term>
<term>Lymphocytes T</term>
</keywords>
<keywords scheme="MESH" qualifier="cytology" xml:lang="en">
<term>Killer Cells, Natural</term>
<term>Leukocytes, Mononuclear</term>
<term>Lymphocytes</term>
<term>T-Lymphocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Cytokines</term>
<term>Facteur de nécrose tumorale alpha</term>
<term>Facteur de transcription STAT-3</term>
<term>Interféron gamma</term>
<term>Interleukine-17</term>
<term>Interleukine-23</term>
<term>Interleukines</term>
<term>Membre-3 du groupe F de la sous-famille-1 de récepteurs nucléaires</term>
<term>Récepteur lymphocytaire T antigène, gamma-delta</term>
<term>Récepteurs aux interleukines</term>
<term>Récepteurs à l'interleukine-12</term>
<term>Récepteurs à l'interleukine-21</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Cell Separation</term>
<term>Flow Cytometry</term>
<term>Humans</term>
<term>Mutation</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Signal Transduction</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Cytométrie en flux</term>
<term>Humains</term>
<term>Mutation</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Séparation cellulaire</term>
<term>Transduction du signal</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Wilson et al. show that individuals with loss-of-function mutations in
<italic>STAT3</italic>
have reduced numbers of peripheral blood MAIT and NKT cells, but not γδ T cells. Residual MAIT cells had normal expression of RORγt, but displayed impaired secretion of IL-17A and IL-17F.</p>
</div>
</front>
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