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在巨细胞病毒特异性人类CD8(+) T细胞中,BY55/CD160不能被视为一种细胞毒性标志物。

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

作者信息

Merino J, Ramírez N, Moreno C, Toledo E, Fernández M, Sánchez-Ibarrola A

机构信息

Department of Immunology, Clínica Universitaria, University of Navarra, Navarra, Spain.

出版信息

Clin Exp Immunol. 2007 Jul;149(1):87-96. doi: 10.1111/j.1365-2249.2007.03387.x. Epub 2007 Apr 11.

Abstract

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)-gamma and interleukin (IL)-7Ralpha/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(+) CD57(-)perforin(-) 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.

摘要

CD160/BY55是一种糖基磷脂酰肌醇(GPI)锚定的细胞膜受体,主要在自然杀伤(NK)细胞中表达。尽管这方面的数据较少,但它在CD8(+) T淋巴细胞中的存在被认为是细胞毒性活性的一个标志物。在本研究中,我们分析了巨细胞病毒(CMV)特异性CD8(+) T细胞亚群中CD160的表达情况。亚群通过CD28和CD57的表达来定义,并表现出不同程度的分化和细胞毒性潜能,这通过穿孔素、干扰素(IFN)-γ和白细胞介素(IL)-7Rα/CD127的表达来评估。我们纳入了具有不同抗病毒免疫反应强度的受试者。结果显示,终末分化的CD28(-) CD57(+)亚群表现出最高水平的穿孔素,其CD160表达水平与记忆性CD28(+) CD57(-)穿孔素(-)细胞相似。CD160(+)细胞与CD160(-)细胞中穿孔素表达的比较表明,在没有CD160的情况下表达显著更高。有趣的是,一名正在经历CMV再激活的患者的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志物。

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