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BY55/CD160 cannot be considered a cytotoxic marker in cytomegalovirus-specific human CD8+ T cells

机译:BY55 / CD160不能被认为是巨细胞病毒特异性人类CD8 + T细胞的细胞毒性标记物

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摘要

CD160/BY55 is a glucosyl-phosphatidylinositol (GPI)-anchored cell membrane receptor that is expressed primarily in natural killer (NK) cells. Its presence in CD8+ T lymphocytes is considered to be a marker of cytotoxic activity, although there are few data in this regard. In the present work, we analysed the expression of CD160 in subpopulations of cytomegalovirus (CMV)-specific CD8+ T cells. Subpopulations were defined by CD28 and CD57 expression and exhibited varying degrees of differentiation and cytotoxic potential, as evaluated by the expression of perforin, interferon (IFN)-γ and interleukin (IL)-7Rα/CD127. We included subjects with different intensities of anti-viral immune response. Results showed that the terminally differentiated CD28 CD57+ subset displaying the highest level of perforin expressed CD160 at a level similar to that of memory CD28+ CD57perforin cells. A comparison of the expression of perforin in CD160+ cells versus CD160 cells showed that expression was significantly higher in the absence of CD160. Interestingly, the CMV-specific CD8+ T cell subset from a patient with ongoing CMV reactivation did not begin to express CD160 until day +92 of the follow-up period. Taken together, our data show that CD160 cannot be considered a cytotoxic marker in CMV-specific CD8+ T cells.
机译:CD160 / BY55是葡萄糖基磷脂酰肌醇(GPI)锚定的细胞膜受体,主要在自然杀伤(NK)细胞中表达。它在CD8 + 淋巴细胞中的存在被认为是细胞毒性活性的标志物,尽管在这方面的数据很少。在本文中,我们分析了CD160在巨细胞病毒(CMV)特异性CD8 + T细胞亚群中的表达。亚群由CD28和CD57表达定义,并表现出不同程度的分化和细胞毒性潜力,通过穿孔素,干扰素(IFN)-γ和白介素(IL)-7Rα/ CD127的表达来评估。我们纳入了具有不同强度的抗病毒免疫反应的受试者。结果显示,终末分化的CD28 CD57 + 子集表现出最高水平的穿孔素表达CD160,其水平类似于记忆CD28 + CD57 穿孔素细胞。比较穿孔素在CD160 + 细胞与CD160 细胞中的表达,结果表明在没有CD160的情况下,穿孔素的表达明显更高。有趣的是,来自持续进行CMV活化的患者的CMV特异性CD8 + T细胞亚群直到随访期的第92天才开始表达CD160。综上所述,我们的数据表明CD160不能被视为CMV特异性CD8 + T细胞中的细胞毒性标记。

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