Decaup Emilie, Duault Caroline, Bezombes Christine, Poupot Mary, Savina Ariel, Olive Daniel, Fournié Jean-Jacques
INSERM/Unité Mixte de Recherche 1037, Centre Recherche en Cancerologie de Toulouse, Toulouse, France; Université Toulouse III Paul-Sabatier, Toulouse, France; ERL 5294 CNRS, Hôpital Purpan, Toulouse, France; Laboratoire d'Excellence 'TOUCAN', France; Institut Carnot 'CALYM', France; Institut de Recherche Roche, Boulogne Billancourt, France.
INSERM/Unité Mixte de Recherche 1037, Centre Recherche en Cancerologie de Toulouse, Toulouse, France; Université Toulouse III Paul-Sabatier, Toulouse, France; ERL 5294 CNRS, Hôpital Purpan, Toulouse, France; Laboratoire d'Excellence 'TOUCAN', France; Institut Carnot 'CALYM', France.
Immunol Lett. 2014 Sep;161(1):133-7. doi: 10.1016/j.imlet.2014.05.011. Epub 2014 Jun 9.
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.
表达TCRVγ9的人类γδ细胞是具有巨大癌症免疫治疗潜力和非常规抗原特异性模式的T淋巴细胞。这些不依赖HLA的淋巴细胞对非肽代谢产物(磷酸抗抗原)和嗜乳脂蛋白3A(BTN3A/CD277)蛋白具有特异性反应。然而,识别这些高度不同的结构是否会触发相同的激活信号通路仍不清楚。在这里,我们结合荧光细胞条形码技术和TCRVγ9(+) T淋巴细胞的磷酸化流式分析,以同时比较磷酸抗抗原(BrHPP)或抗BTN3A(单克隆抗体20.1)激活后几种信号磷酸化蛋白的水平。该方法表明,涉及ZAP70、PLCγ2、Akt、NFκB p65、MAPK p38和Erk1的相同信号通路可由这两种刺激中的任何一种诱导。这些数据有力地表明,TCRVγ9(+) T淋巴细胞通过相同的识别过程检测磷酸抗抗原和嗜乳脂蛋白A3。