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Immunogenetics of Aging’: report on the activities of theud15th International HLA and Immunogenetics Working Groupudand 15th International HLA and Immunogenetics Workshop

机译:衰老的免疫遗传学”:报告 ud的活动第15届国际HLA和免疫遗传学工作组和第15届国际HLA和免疫遗传学研讨会

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摘要

‘Immunogenetics of Aging’ is a component that was first included in the 14thudInternational HLA and Immunogenetics Workshop (IHIWS) and developed furtherudwithin the 15th Workshop. The aim of this component was to assess the impact ofudhuman leukocyte antigen (HLA) genes, cytokine genes, and some innate immunityudgenes such as killer-cell immunoglobulin-like receptors (KIRs) and mannose-bindingudlectin 2 (MBL2) in successful aging and their contribution to the better understandingudof immune dysfunction in old age. Within the 15th IHIWS new populations wereudincluded in the analysis. Additional cytokine gene polymorphisms were assessedudand innate immunity genes were analyzed for possible relevance in longevity. Theudresults showed that longevity might be associated with anti-inflammatory cytokineudgene profiles, decreased frequency of interleukin-10 (IL-10) and transforming growthudfactor-B1 haplotypes associated with a low level of gene expression, and increasedudfrequency of haplotypes determining a high level of expression. Extended tumorudnecrosis factor-A and IL-12B genotypes were also likely relevant to longevity. Dataudalso showed that innate immunity genes are associated with susceptibility to infectionsudin the elderly and showed that these genes might be an important genetic marker inudaging. Decreased frequencies of KIR2DS5 and A1B10 haplotypes, and an increasedudproportion of MBL2-deficient haplotypes were found in the group with higherudcytomegalovirus-specific IgG antibody levels. Together, these studies emphasize theudrelevance of genes regulating immune functions in maintaining human longevity andudstress the importance of further clarifying their impact on successful aging.
机译:“衰老的免疫遗传学”是第14届国际HLA和免疫遗传学研讨会(IHIWS)中首次包含的内容,并在第15届研讨会中进一步发展。该组件的目的是评估 udhuman白细胞抗原(HLA)基因,细胞因子基因和某些先天免疫 udgenes(例如杀伤细胞免疫球蛋白样受体(KIR)和甘露糖结合 udlectin 2(MBL2) )在成功的衰老过程中发挥作用,并有助于更好地理解老年人的免疫功能障碍。在第15届IHIWS中,新人群被纳入分析。评估了其他细胞因子基因多态性 ud,并分析了天然免疫基因与长寿的可能相关性。 结果表明,长寿可能与抗炎细胞因子/芥菜谱,白细胞介素10(IL-10)频率降低和转化生长 udfactor-B1单倍型相关,与基因表达水平低相关, ud频率增加确定高水平表达的单倍型。延长的肿瘤坏死因子-A和IL-12B基因型也可能与寿命有关。数据也表明,先天免疫基因与老年人的感染易感性有关,并表明这些基因可能是老年人感染的重要遗传标记。在具有较高巨细胞巨细胞病毒特异性IgG抗体水平的组中,发现KIR2DS5和A1B10单倍型的频率降低,以及MBL2缺陷单倍型的增加不成比例。总之,这些研究强调了调节免疫功能的基因与维持人类寿命的不相关性,并强调了进一步阐明其对成功衰老的影响的重要性。

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