Miyadera Hiroko, Noguchi Emiko, Mizokami Masashi, Tokunaga Katsushi
Department of Medical Genetics, Faculty of Medicine, University of Tsukuba.
Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine.
Nihon Rinsho Meneki Gakkai Kaishi. 2017;40(1):35-39. doi: 10.2177/jsci.40.35.
Genes encoding the human leukocyte antigens (HLA) are associated with diverse immunological disorders, including autoimmune diseases and infections. Recently, significant progresses have been made in the HLA typing technologies through the use of next generation sequencers. The reliable platforms for the SNP-based imputation of HLA genotypes have also been established. These technical advancements should enable further identification of HLA associations with diseases. One of the remaining questions is the mechanism through which HLA confer disease susceptibility. As a first step toward comprehensive understanding of functional variations among HLA allele products, we established a protocol to analyze the HLA-binding peptides through quantification of cell-surface HLA expression in an engineered cell line. In this article, we summarize the overview of the cell-surface HLA expression assay, which we plan to use for screening and collection of HLA-peptide interaction profiles for large sets of HLA alleles and peptides.
编码人类白细胞抗原(HLA)的基因与多种免疫紊乱相关,包括自身免疫性疾病和感染。最近,通过使用新一代测序仪,HLA分型技术取得了重大进展。基于单核苷酸多态性(SNP)的HLA基因型推断的可靠平台也已建立。这些技术进步应能进一步鉴定HLA与疾病的关联。剩下的问题之一是HLA赋予疾病易感性的机制。作为全面了解HLA等位基因产物功能变异的第一步,我们建立了一种通过定量工程细胞系中细胞表面HLA表达来分析HLA结合肽的方案。在本文中,我们总结了细胞表面HLA表达测定的概述,我们计划将其用于筛选和收集大量HLA等位基因和肽的HLA-肽相互作用谱。