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外周血白细胞中,HLA - A和HLA - B转录随衰老而减少。

HLA-A and HLA-B transcription decrease with ageing in peripheral blood leucocytes.

作者信息

Le Morvan C, Cogné M, Drouet M

机构信息

Laboratoire d'Immunologie et Immunogénétique CNRS UMR 6101, Limoges, France.

出版信息

Clin Exp Immunol. 2001 Aug;125(2):245-50. doi: 10.1046/j.1365-2249.2001.01610.x.

Abstract

Immunosenescence involves modifications of humoral and cellular immunity. In a previous study, we have shown a locus-dependent reduction of HLA class-I cell surface expression on peripheral lymphocytes and monocytes with advancing age. Here we report the quantitative analysis of HLA-A and -B transcripts from PBL of 54 healthy subjects aged 21-90 years. Using a competitive RT-PCR method, we observed a significant decrease of HLA-A (P < 0.0001) and -B (P = 0.0025) mRNA contents with increasing age. Secondly, to investigate this locus-dependent alteration of HLA class-I transcription, we performed EMSA using nuclear extracts from PBL of five young (24-31-year-old) and 5 elderly (58-69 years old) donors with locus A and B sequences of the Enh-A as probes. No qualitative variation of EMSA profiles appeared between the two groups of donors with 6 and 4 bandshift for the locus A and B, respectively. Quantitatively, we observed a significant increase of B4 intensity in the elderly group compared to the young group (P < 0.05). These results suggest that the variation of DNA binding protein could contribute to the lower transcription of HLA-A and -B with ageing. These alterations of HLA class-I expression at the transcriptional level could lead to the unresponsiveness of CD8 T cells due to default of antigen presentation with ageing.

摘要

免疫衰老涉及体液免疫和细胞免疫的改变。在之前的一项研究中,我们已经表明,随着年龄的增长,外周淋巴细胞和单核细胞上HLA-I类分子的细胞表面表达存在基因座依赖性降低。在此,我们报告了对54名年龄在21至90岁的健康受试者外周血淋巴细胞(PBL)中HLA-A和 -B转录本的定量分析。使用竞争性逆转录聚合酶链反应(RT-PCR)方法,我们观察到随着年龄的增长,HLA-A(P < 0.0001)和 -B(P = 0.0025)的mRNA含量显著下降。其次,为了研究HLA-I类转录的这种基因座依赖性改变,我们以Enh-A的A和B基因座序列为探针,使用来自5名年轻(24至31岁)和5名老年(58至69岁)供体的PBL核提取物进行了电泳迁移率变动分析(EMSA)。两组供体之间EMSA图谱没有定性差异,A基因座和B基因座分别出现6条和4条带移位。定量分析显示,与年轻组相比,老年组B4强度显著增加(P < 0.05)。这些结果表明,DNA结合蛋白的变化可能导致衰老过程中HLA-A和 -B转录降低。HLA-I类表达在转录水平的这些改变可能由于衰老导致抗原呈递缺陷而导致CD8 T细胞无反应性。

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