Literature DB >> 26123353

Adaptive Immune-like γ/δ T Lymphocytes Share Many Common Features with Their α/β T Cell Counterparts.

Amélie Lombes1, Aurélie Durand1, Céline Charvet1, Matthieu Rivière1, Nelly Bonilla1, Cédric Auffray1, Bruno Lucas1, Bruno Martin2.   

Abstract

To better apprehend γ/δ T cell biological functions in the periphery, it appears crucial to identify markers highlighting the existence of distinct phenotypic and functional γ/δ T cell subsets. Interestingly, the expression of CD44 and Ly-6C subdivides murine peripheral γ/δ T cells into several subsets, with Ly-6C(-) CD44(hi) γ/δ T cells corresponding to the IL-17-producing CD27(-) γ/δ T cell subset exhibiting innate-like features. By comparing the other subsets to naive and memory CD8(+) α/β T cells, in this study, we show that Ly-6C(- or +) CD44(lo) and Ly-6C(+)CD44(hi) γ/δ T cells greatly resemble, and behave like, their CD8(+) α/β T cell counterparts. First, like memory CD8(+) α/β T cells, Ly-6C(+)CD44(hi) γ/δ T cells are sparse in the thymus but largely increased in proportion in tissues. Second, similarly to naive CD8 α/β T cells, CD44(lo) γ/δ T cells are poorly cycling in vivo in the steady state, and their proportion declines with age in secondary lymphoid organs. Third, CD44(lo) γ/δ T cells undergo spontaneous proliferation and convert to a memory-like Ly-6C(+)CD44(hi) phenotype in response to lymphopenia. Finally, CD44(lo) γ/δ T cells have an intrinsic high plasticity as, upon appropriate stimulation, they are capable of differentiating nonetheless into Th17-like and Th1-like cells but also into fully functional Foxp3(+) induced regulatory T cell-like γ/δ T cells. Thus, peripheral CD27(+) γ/δ T cells, commonly considered as a functionally related T cell compartment, actually share many common features with adaptive α/β T cells, as both lineages include naive-like and memory-like lymphocytes with distinct phenotypic, functional, and homeostatic characteristics.
Copyright © 2015 by The American Association of Immunologists, Inc.

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Year:  2015        PMID: 26123353     DOI: 10.4049/jimmunol.1500375

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  14 in total

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Authors:  Daniel G Pellicci; Hui-Fern Koay; Stuart P Berzins
Journal:  Nat Rev Immunol       Date:  2020-06-24       Impact factor: 53.106

Review 2.  Developmental origins of murine γδ T-cell subsets.

Authors:  Nital Sumaria; Stefania Martin; Daniel J Pennington
Journal:  Immunology       Date:  2019-01-21       Impact factor: 7.397

3.  Development of interleukin-17-producing Vγ2+ γδ T cells is reduced by ICOS signaling in the thymus.

Authors:  Terkild Brink Buus; Jonas Damgård Schmidt; Charlotte Menné Bonefeld; Carsten Geisler; Jens Peter Holst Lauritsen
Journal:  Oncotarget       Date:  2016-04-12

4.  Profiling the lymphoid-resident T cell pool reveals modulation by age and microbiota.

Authors:  Aurélie Durand; Alexandra Audemard-Verger; Vincent Guichard; Raphaël Mattiuz; Arnaud Delpoux; Pauline Hamon; Nelly Bonilla; Matthieu Rivière; Jérôme Delon; Bruno Martin; Cédric Auffray; Alexandre Boissonnas; Bruno Lucas
Journal:  Nat Commun       Date:  2018-01-04       Impact factor: 14.919

5.  Vγ4+γδT Cells Aggravate Severe H1N1 Influenza Virus Infection-Induced Acute Pulmonary Immunopathological Injury via Secreting Interleukin-17A.

Authors:  Chunxue Xue; Mingjie Wen; Linlin Bao; Hui Li; Fengdi Li; Meng Liu; Qi Lv; Yunqing An; Xulong Zhang; Bin Cao
Journal:  Front Immunol       Date:  2017-08-31       Impact factor: 7.561

6.  Three distinct developmental pathways for adaptive and two IFN-γ-producing γδ T subsets in adult thymus.

Authors:  Terkild Brink Buus; Niels Ødum; Carsten Geisler; Jens Peter Holst Lauritsen
Journal:  Nat Commun       Date:  2017-12-04       Impact factor: 14.919

7.  Strong TCRγδ Signaling Prohibits Thymic Development of IL-17A-Secreting γδ T Cells.

Authors:  Nital Sumaria; Capucine L Grandjean; Bruno Silva-Santos; Daniel J Pennington
Journal:  Cell Rep       Date:  2017-06-20       Impact factor: 9.423

8.  Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition).

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Luka Čičin-Šain; Mario Clerici; Federico S Colombo; Laura Cook; Anne Cooke; Andrea M Cooper; Alexandra J Corbett; Antonio Cosma; Lorenzo Cosmi; Pierre G Coulie; Ana Cumano; Ljiljana Cvetkovic; Van Duc Dang; Chantip Dang-Heine; Martin S Davey; Derek Davies; Sara De Biasi; Genny Del Zotto; Gelo Victoriano Dela Cruz; Michael Delacher; Silvia Della Bella; Paolo Dellabona; Günnur Deniz; Mark Dessing; James P Di Santo; Andreas Diefenbach; Francesco Dieli; Andreas Dolf; Thomas Dörner; Regine J Dress; Diana Dudziak; Michael Dustin; Charles-Antoine Dutertre; Friederike Ebner; Sidonia B G Eckle; Matthias Edinger; Pascale Eede; Götz R A Ehrhardt; Marcus Eich; Pablo Engel; Britta Engelhardt; Anna Erdei; Charlotte Esser; Bart Everts; Maximilien Evrard; Christine S Falk; Todd A Fehniger; Mar Felipo-Benavent; Helen Ferry; Markus Feuerer; Andrew Filby; Kata Filkor; Simon Fillatreau; Marie Follo; Irmgard Förster; John Foster; Gemma A Foulds; Britta Frehse; Paul S Frenette; Stefan Frischbutter; Wolfgang Fritzsche; 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9.  Variegated Transcription of the WC1 Hybrid PRR/Co-Receptor Genes by Individual γδ T Cells and Correlation With Pathogen Responsiveness.

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Journal:  Front Immunol       Date:  2018-05-07       Impact factor: 7.561

10.  Lymph node γδ and αβ CD8+ T cells share migratory properties.

Authors:  Milas Ugur; Anne Kaminski; Oliver Pabst
Journal:  Sci Rep       Date:  2018-06-12       Impact factor: 4.379

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