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Phosphoantigens and butyrophilin 3A1 induce similar intracellular activation signaling in human TCRVγ9+ γδ T lymphocytes

Authors :
Emilie Decaup
Daniel Olive
Mary Poupot
Caroline Duault
Jean-Jacques Fournié
Christine Bezombes
Ariel Savina
Centre de Recherches en Cancérologie de Toulouse (CRCT)
Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Immunité et cancer (U932)
Université Paris Descartes - Paris 5 (UPD5)-Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
Centre de Recherche en Cancérologie de Marseille (CRCM)
Aix Marseille Université (AMU)-Institut Paoli-Calmettes
Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Université Paris Descartes - Paris 5 (UPD5)-Institut Curie-Institut National de la Santé et de la Recherche Médicale (INSERM)
Poupot, Mary
Source :
Immunology Letters, Immunology Letters, Elsevier, 2014, 161 (1), pp.133-137. ⟨10.1016/j.imlet.2014.05.011⟩, Immunology Letters, 2014, 161 (1), pp.133-137. ⟨10.1016/j.imlet.2014.05.011⟩
Publication Year :
2014
Publisher :
HAL CCSD, 2014.

Abstract

International audience; Human γδ cells expressing TCRVγ9 are T lymphocytes with great potential for cancer immunotherapy and unconventional pattern of antigen specificity. These HLA-unrestricted lymphocytes are specifically reactive to non-peptide metabolites (phosphoantigens) and to the butyrophilin 3A (BTN3A/CD277) protein. Whether recognition of such highly different structures trigger the same activation signaling pathway remains unclear, however. Here we combined fluorescent cell barcoding and phosphoflow analysis of TCRVγ9(+) T lymphocytes to compare simultaneously the level of several signaling phosphoproteins after activation by phosphoantigen (BrHPP) or by anti-BTN3A (monoclonal antibody 20.1). This approach shows that the same pathways involving ZAP70, PLCγ2, Akt, NFκB p65, MAPK p38 and Erk1, were induced by either of these stimuli. These data strongly suggest the TCRVγ9(+) T lymphocytes detect phosphoantigens and butyrophilin A3 by the same recognition process.

Details

Language :
English
ISSN :
01652478
Database :
OpenAIRE
Journal :
Immunology Letters, Immunology Letters, Elsevier, 2014, 161 (1), pp.133-137. ⟨10.1016/j.imlet.2014.05.011⟩, Immunology Letters, 2014, 161 (1), pp.133-137. ⟨10.1016/j.imlet.2014.05.011⟩
Accession number :
edsair.doi.dedup.....a97762d8caf2c968ed12593d6eeb18ec
Full Text :
https://doi.org/10.1016/j.imlet.2014.05.011⟩