Literature DB >> 31331679

17th IHIW component "Immunogenetics of Ageing" - New NGS data.

Milena Ivanova1, Lisa E Creary2, Bushra Al Hadra3, Tsvetelin Lukanov3, Michela Mazzocco4, Nicoletta Sacchi4, Reem Ameen5, Salem Al-Shemmari5, Ana Moise6, Larisa Denisa Ursu6, Ileana Constantinescu6, Tamara Vayntrub7, Marcelo A Fernández-Viňa2, Velizar Shivarov8, Elissaveta Naumova3.   

Abstract

The 'Immunogenetics of Aging' project is a component introduced in the 14th International HLA and Immunogenetics Workshop (IHIW) and developed further within subsequent workshops. The aim was to determine the relevance of immunogenetic markers, focusing on HLA, cytokine genes, and some innate immunity genes, for successful aging and an increased capacity to reach the extreme limits of life-span. Within the 17th IHIW we applied Next Generation Sequencing methods to refine further HLA associations at allele level in longevity, and to extend our knowledge to additional loci such as HLA-DQA1, HLA-DPB1 and HLA-DPA1. Analysis of relatively small number of healthy elderly and young controls from four populations showed that some HLA class I and class II alleles were significantly positively associated with healthy aging. Additionally we observed statistically significant differences in HLA allele distribution when the analysis was performed separately in elderly females and males compared to sex-matched young controls. Haplotypes, probably associated with better control of viral and malignant diseases were increased in the elderly sample. These preliminary NGS data could confirm our hypotheses that survival and longevity might be associated with selection of HLA alleles and haplotypes conferring disease resistance or susceptibility. Therefore HLA alleles and haplotypes could be informative immunogenetic markers for successful ageing.
Copyright © 2019 American Society for Histocompatibility and Immunogenetics. All rights reserved.

Entities:  

Keywords:  Ageing; HLA; Longevity; NGS

Mesh:

Substances:

Year:  2019        PMID: 31331679      PMCID: PMC6773488          DOI: 10.1016/j.humimm.2019.07.287

Source DB:  PubMed          Journal:  Hum Immunol        ISSN: 0198-8859            Impact factor:   2.850


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