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Decreased expression of 20-kD homologous restriction factor (HRF20, CD59) on T lymphocytes in Epstein–Barr virus (EBV)-induced infectious mononucleosis

机译:在爱泼斯坦-巴尔病毒(EBV)引起的感染性单核细胞增多症的T淋巴细胞上20 kD同源限制因子(HRF20,CD59)的表达降低

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摘要

HRF20 (CD59) is one of the membrane-associated complement regulatory proteins. The characteristic function of CD59 is to prevent membrane attack complex (MAC) formation on the cell surface and to protect the cell from complement-mediated cell lysis. We examined the expression of CD59 antigen on T cell subpopulations in patients with acute infectious mononucleosis (IM) and analysed the relationship between the amount of CD59 expression and activation-induced cell death of mature T cells with apoptosis. Decreased expression of CD59 on CD8+ T cells, especially on CD45RO+ and HLA-DR+ activated T cells, was marked in acute IM patients. In contrast, activated CD4+ T cells from IM patients expressed as much CD59 antigen as CD4+ T cells from healthy volunteers. After incubation-induced cell death, viable CD8+ T cells showed normal amounts of CD59 antigen on their surface. CD59dim CD8+ T cells were more susceptible to apoptosis than CD59bright CD8+ T cells. These findings suggest that decreased expression of CD59 on CD8+ T cells may discriminate the susceptibility of activated CD8+ T cells to activation-induced cell death in IM.
机译:HRF20(CD59)是与膜相关的补体调节蛋白之一。 CD59的特征功能是防止在细胞表面形成膜攻击复合物(MAC),并保护细胞免受补体介导的细胞裂解。我们检查了急性感染性单核细胞增多症(IM)患者T细胞亚群上CD59抗原的表达,并分析了CD59表达量与激活的成熟T细胞凋亡诱导的细胞死亡之间的关系。在急性IM患者中,CD59在CD8 + T细胞,特别是在CD45RO +和HLA-DR +活化的T细胞上的表达降低。相反,IM患者的活化CD4 + T细胞表达的CD59抗原与健康志愿者的CD4 + T细胞一样多。温育诱导的细胞死亡后,存活的CD8 + T细胞在其表面显示正常量的CD59抗原。 CD59dim CD8 + T细胞比CD59bright CD8 + T细胞更容易发生凋亡。这些发现表明,CD8 + T细胞上CD59表达的降低可能会区分活化的CD8 + T细胞对IM中活化诱导的细胞死亡的敏感性。

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