天然免疫基因的系统表达谱分析揭示了外周血和肠道白细胞中复杂的免疫衰老模式。

Systematic expression profiling of innate immune genes defines a complex pattern of immunosenescence in peripheral and intestinal leukocytes.

作者信息

Rosenstiel P, Derer S, Till A, Häsler R, Eberstein H, Bewig B, Nikolaus S, Nebel A, Schreiber S

机构信息

Institute for Clinical Molecular Biology, Christian-Albrechts-University Kiel, Kiel, Germany.

出版信息

Genes Immun. 2008 Mar;9(2):103-14. doi: 10.1038/sj.gene.6364454. Epub 2008 Jan 24.

Abstract

Immunosenescence is characterized by a quantitative decline of adequate immune responses, which renders the elderly individual particularly susceptible to bacterial, viral and fungal pathogens. Whereas changes of the aging adaptive immune system (for example, reduced immunoglobulin secretion) have been extensively characterized, alterations of the innate immune system are still poorly understood. The aim of the present study was to systematically examine mRNA expression levels of innate immune genes and proinflammatory cytokines in peripheral and intestinal leukocytes of subjects of different ages. In both, whole blood samples and in colonic biopsies most of the Toll-like receptors (TLRs) and nucleotide-binding and oligomerization domain-like receptors (NLRs) transcript levels were significantly downregulated in elderly subjects (90-99 years). Older individuals, when compared to the younger, exhibited an increased expression and/or secretion of proinflammatory cytokines by peripheral and intestinal leukocytes as well as an increased level of nuclear factor-kappaB activation in colonic biopsies. The observed downregulation of TLRs and NLRs during the aging process may contribute to the lack of effective recognition of invading pathogens or the commensal flora. This effect results in aberrant secondary immune cell activation and could significantly contribute to morbidity and mortality at advanced age.

摘要

免疫衰老的特征是适当免疫反应的数量下降,这使得老年人特别容易受到细菌、病毒和真菌病原体的侵袭。虽然衰老的适应性免疫系统的变化(例如免疫球蛋白分泌减少)已得到广泛描述,但对先天性免疫系统的改变仍知之甚少。本研究的目的是系统地检测不同年龄受试者外周血和肠道白细胞中先天性免疫基因和促炎细胞因子的mRNA表达水平。在全血样本和结肠活检组织中,大多数Toll样受体(TLR)和核苷酸结合寡聚化结构域样受体(NLR)的转录水平在老年受试者(90-99岁)中均显著下调。与年轻人相比,老年人外周血和肠道白细胞中促炎细胞因子的表达和/或分泌增加,结肠活检组织中核因子-κB的激活水平也升高。在衰老过程中观察到的TLR和NLR下调可能导致对入侵病原体或共生菌群缺乏有效识别。这种效应会导致异常的继发性免疫细胞激活,并可能显著增加老年人的发病率和死亡率。

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