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第十四届国际人类白细胞抗原与免疫遗传学研讨会:衰老免疫遗传学报告

14th International HLA and Immunogenetics Workshop: report on the immunogenetics of aging.

作者信息

Naumova E, Pawelec G, Ivanova M, Constantinescu I, Bogunia-Kubik K, Lange A, Qguz F, Carin M

机构信息

Central Laboratory of Clinical Immunology, University Hospital Alexandrovska, Sofia, Bulgaria.

出版信息

Tissue Antigens. 2007 Apr;69 Suppl 1:304-10. doi: 10.1111/j.1399-0039.2006.00783.x.

DOI:10.1111/j.1399-0039.2006.00783.x
PMID:17445222
Abstract

The 'Immunogenetics of Aging' is a newly included component within the 14th International HLA and Immunogenetics Workshop. The aim of this component was to determine the contribution of human leukocyte antigen (HLA), cytokine genes and other major histocompatibility complex-encoded loci to successful aging and to determine an increased capacity to reach the extreme limits of life span. Two main data sets from four European populations were included in this study: unrelated healthy elderly individuals and ethnically matched young controls, and families with longevity members. Analysis was focused on HLA class I and II and cytokine gene polymorphisms. Preliminary results showed increased frequencies of DRB111- and DRB16-associated haplotypes that were found to be protective for autoimmune diseases in some populations. Additionally, in families with longevity members, alleles and haplotypes positively associated with autoimmunity were not observed. Analysis of cytokine gene polymorphisms showed prevalence of anti-inflammatory profiles in healthy elderly individuals. Inheritance of extended haplotypes in families with longevity members allowed the identification of immunogenetic profiles that could be predictive for longevity. These preliminary studies indicate the relevance of genes regulating immune functions in human longevity and the importance of clarifying further their impact in successful aging.

摘要

“衰老的免疫遗传学”是第14届国际人类白细胞抗原与免疫遗传学研讨会新纳入的一个部分。该部分的目的是确定人类白细胞抗原(HLA)、细胞因子基因和其他主要组织相容性复合体编码基因座对成功衰老的贡献,并确定达到寿命极限的能力增强情况。本研究纳入了来自四个欧洲人群的两个主要数据集:无关的健康老年人个体和种族匹配的年轻对照,以及有长寿成员的家庭。分析重点是HLAⅠ类和Ⅱ类以及细胞因子基因多态性。初步结果显示,在某些人群中发现与DRB111和DRB16相关的单倍型频率增加,这些单倍型对自身免疫性疾病具有保护作用。此外,在有长寿成员的家庭中,未观察到与自身免疫呈正相关的等位基因和单倍型。细胞因子基因多态性分析显示健康老年人个体中抗炎谱占优势。对有长寿成员的家庭中扩展单倍型的遗传分析,有助于识别可能预测长寿的免疫遗传特征。这些初步研究表明调节免疫功能的基因在人类长寿中的相关性,以及进一步阐明其对成功衰老影响的重要性。

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