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在膜性肾病中,深口袋不一定是好事:修饰等位基因的证据。

Deep pockets are not necessarily a good thing in membranous nephropathy: evidence for a modifier allele.

机构信息

Department of Medicine, Renal Section, Boston University School of Medicine and Boston Medical Center, Boston, Massachusetts, USA.

Department of Medicine, Renal Section, Boston University School of Medicine and Boston Medical Center, Boston, Massachusetts, USA.

出版信息

Kidney Int. 2018 Nov;94(5):855-857. doi: 10.1016/j.kint.2018.07.010.

Abstract

Risk (or susceptibility) alleles for primary membranous nephropathy exist within the DQ and DR loci of the human leukocyte antigen (HLA) region of chromosome 6. The discussed study identifies a novel allele, HLA DRB1*1502, in a Han Chinese cohort that acts as a modifier allele by associating not with the phenotype of membranous nephropathy, but rather with the severity of disease. This commentary addresses the potential biologic aspects of these new data.

摘要

原发性膜性肾病的风险(或易感性)等位基因存在于人类白细胞抗原(HLA)第 6 号染色体的 DQ 和 DR 基因座中。该研究在一个汉族队列中发现了一个新的 HLA-DRB1*1502 等位基因,它作为一个修饰等位基因起作用,与膜性肾病的表型无关,而是与疾病的严重程度相关。本评论探讨了这些新数据的潜在生物学方面。

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