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1型自身免疫性肝炎的早发具有很强的遗传影响:HLA和KIR基因的作用。

The early onset of type 1 autoimmune hepatitis has a strong genetic influence: role of HLA and KIR genes.

作者信息

Podhorzer A, Paladino N, Cuarterolo M L, Fainboim H A, Paz S, Theiler G, Capucchio M, López S I, Machicote A, Montal S, Podesta G, Fainboim L

机构信息

Instituto de Inmunología, Genética y Metabolismo (INIGEM-CONICET), Hospital de Clínicas "José de San Martín", Universidad de Buenos Aires, Buenos Aires, Argentina.

Hospital Nacional de Pediatría J. P. Garrahan, Buenos Aires, Argentina.

出版信息

Genes Immun. 2016 Apr;17(3):187-92. doi: 10.1038/gene.2016.7. Epub 2016 Feb 18.

Abstract

We have previously reported a strong association between HLA-DRB11301 and type 1 pediatric autoimmune hepatitis (PAH) and between HLA-DR0405 and adult autoimmune hepatitis (AAH). Because human killer cell immunoglobulin-like receptors are known to be associated with susceptibility to autoimmune diseases, we investigated the frequencies of HLA-A, B, C, DRB1 and KIR genes in 144 type 1 PAH and 86 AAH patients, which were compared with 273 healthy controls. We demonstrated in PAH the increased frequency of the functional form of KIR2DS4-Full Length (KIR2DS4-FL), which in combination with HLA-DRB11301 revealed a strong synergistic effect (odds ratio=36.5). PAH-KIR2DS4-FL+ subjects have shown an increased frequency of their putative HLA-C02, 04 and 06 ligands. KIR analysis of PAH also revealed a decreased frequency of KIR2DL2 gene and its ligand. In contrast, AAH cases have shown a weaker increased frequency of KIR2DS4-FL, a lack of synergistic effect with HLA class II antigens and a moderate association with HLA-DRB1*0405. Of note, we demonstrated that liver T cells have a unique pattern of KIR expression. These results show a KIR gene involved in autoimmune hepatitis and suggest a stronger genetic influence for the early onset type I autoimmune hepatitis.

摘要

我们之前报道过HLA - DRB11301与1型儿童自身免疫性肝炎(PAH)以及HLA - DR0405与成人自身免疫性肝炎(AAH)之间存在密切关联。由于已知人类杀伤细胞免疫球蛋白样受体与自身免疫性疾病的易感性相关,我们调查了144例1型PAH患者和86例AAH患者中HLA - A、B、C、DRB1和KIR基因的频率,并与273名健康对照进行了比较。我们在PAH患者中发现KIR2DS4全长功能形式(KIR2DS4 - FL)的频率增加,其与HLA - DRB11301联合显示出强烈的协同效应(优势比 = 36.5)。PAH - KIR2DS4 - FL +受试者显示其假定的HLA - C02、04和06配体的频率增加。对PAH的KIR分析还显示KIR2DL2基因及其配体的频率降低。相比之下,AAH病例中KIR2DS4 - FL的频率增加较弱,与HLA II类抗原缺乏协同效应,且与HLA - DRB1*0405存在中度关联。值得注意的是,我们证明肝脏T细胞具有独特的KIR表达模式。这些结果表明KIR基因参与自身免疫性肝炎,并提示I型自身免疫性肝炎早期发病的遗传影响更强。

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