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重症IgA肾病患儿免疫球蛋白重链转换区基因的多态性

Polymorphism of immunoglobulin heavy chain switch region gene in children with severe IgA nephropathy.

作者信息

Shimomura M, Yoshikawa N, Iijima K, Nakamura H, Miyazaki M, Sakai H

机构信息

Department of Pediatrics, Kobe University School of Medicine, Japan.

出版信息

Clin Nephrol. 1995 Apr;43(4):211-5.

PMID:7606874
Abstract

We examined restriction fragment length polymorphisms (RFLPs) of the switch region genes of the IgM (S mu) and IgA1 (S alpha 1) heavy chain in 78 Japanese children with IgA nephropathy and 88 normal Japanese controls. Genomic DNA obtained from patients and controls was digested with the restriction endonuclease SacI, transferred to nylon membrane using Southern blot procedure, and hybridized with a DNA probe homologous to S mu. This probe detects RFLPs at the S mu and S alpha 1 loci by enhanced chemiluminescence. The genotypic frequency of the S mu and S alpha 1 alleles in patients with IgA nephropathy was similar to normal controls. However, there was a significant association of genotypes with the pathological severity. There was a decreased frequency of the 2.6/2.1 kb S mu heterozygous genotype in patients showing diffuse mesangial proliferation compared to controls or patients showing minimal or focal mesangial proliferation. Our results suggest that immunoglobulin heavy chain switch region genes may not influence susceptibility to IgA nephropathy in children, but may influence the pathological expression of childhood IgA nephropathy.

摘要

我们检测了78例日本IgA肾病患儿及88名正常日本对照者IgM(Sμ)和IgA1(Sα1)重链转换区基因的限制性片段长度多态性(RFLP)。从患者和对照者获取的基因组DNA用限制性内切酶SacI消化,采用Southern印迹法转移至尼龙膜,并用与Sμ同源的DNA探针杂交。该探针通过增强化学发光检测Sμ和Sα1位点的RFLP。IgA肾病患者中Sμ和Sα1等位基因的基因型频率与正常对照相似。然而,基因型与病理严重程度存在显著关联。与对照者或表现为轻微或局灶性系膜增生的患者相比,表现为弥漫性系膜增生的患者中2.6/2.1 kb Sμ杂合基因型的频率降低。我们的结果提示,免疫球蛋白重链转换区基因可能不影响儿童IgA肾病的易感性,但可能影响儿童IgA肾病的病理表现。

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