Masutani Kohsuke, Miyake Katsuhisa, Nakashima Hitoshi, Hirano Tadashi, Kubo Michiaki, Hirakawa Makoto, Tsuruya Kazuhiko, Fukuda Kyoichi, Kanai Hidetoshi, Otsuka Takeshi, Hirakata Hideki, Iida Mitsuo
Departments of Medicine and Clinical Science and Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Am J Kidney Dis. 2003 Feb;41(2):371-9. doi: 10.1053/ajkd.2003.50046.
Cytokines have an important role in the pathogenesis and disease progression of immunoglobulin A (IgA) nephropathy. The aim of this study is to investigate the impact of gene polymorphisms of T helper cell subtype 1 (T(H)1)/T(H)2 cytokines, interferon-gamma (IFN-gamma), and interleukin-4 (IL-4) on IgA nephropathy in Japanese patients.
We investigated IFN-gamma gene (IFNG) and IL-4 gene (IL4) polymorphisms in 96 patients with biopsy-confirmed IgA nephropathy who were followed-up for more than 3 years in our outpatient clinic and 61 healthy controls by polymerase chain reaction and direct sequencing methods. IFNG polymorphism was characterized as a microsatellite of intron 1. Four alleles were identified and designated IFNG 112, 114, 116, and 118, corresponding to 12, 13, 14, and 15 repeats, respectively. A variable number of tandem repeat (VNTR) polymorphisms of IL4 also were studied, and alleles were designated IL4 B1 and B2, corresponding to 2 and 3 repeats, respectively.
In patients with IgA nephropathy, IFNG 114 allele and IFNG 114(+/+) genotype frequencies were significantly greater than in the healthy control group (60% versus 45%; P < 0.01 and 43% versus 23%; P < 0.05, respectively), but there was no difference between the IgA nephropathy and healthy control groups in frequencies of both IL4 VNTR allele and genotype. However, frequencies of IL4 B1 allele and B1/B1 genotype in patients with progressive IgA nephropathy (end-stage renal disease or doubling of serum creatinine level; n = 34) were significantly greater than corresponding values in the nonprogression group (n = 62; 79% versus 61%; P < 0.01 and 59% versus 34%; P < 0.05, respectively). We could not confirm an association between IgA nephropathy and polymorphisms of genes involved in the renin-angiotensin system.
Our results suggest that IFN-gamma and IL-4 gene polymorphisms could influence disease susceptibility and disease progression in IgA nephropathy in Japanese patients. Am J Kidney Dis 41:371-379.
细胞因子在免疫球蛋白A(IgA)肾病的发病机制和疾病进展中起重要作用。本研究旨在探讨辅助性T细胞1型(Th1)/Th2细胞因子、干扰素-γ(IFN-γ)和白细胞介素-4(IL-4)的基因多态性对日本IgA肾病患者的影响。
我们采用聚合酶链反应和直接测序方法,对96例经活检确诊为IgA肾病且在我院门诊随访3年以上的患者以及61例健康对照者进行了IFN-γ基因(IFNG)和IL-4基因(IL4)多态性检测。IFNG多态性表现为内含子1的微卫星。共鉴定出4个等位基因,分别命名为IFNG 112、114、116和118,分别对应12、13、14和15个重复序列。还研究了IL4的可变数目串联重复(VNTR)多态性,等位基因分别命名为IL4 B1和B2,分别对应2个和3个重复序列。
在IgA肾病患者中,IFNG 114等位基因和IFNG 114(+/+)基因型频率显著高于健康对照组(分别为60%对45%;P<0.01和43%对23%;P<0.05),但IL4 VNTR等位基因和基因型频率在IgA肾病组与健康对照组之间无差异。然而,进行性IgA肾病患者(终末期肾病或血清肌酐水平翻倍;n=34)中IL4 B1等位基因和B1/B1基因型频率显著高于非进展组(n=62;分别为79%对61%;P<0.01和59%对34%;P<0.05)。我们未能证实IgA肾病与肾素-血管紧张素系统相关基因多态性之间的关联。
我们的结果提示,IFN-γ和IL-4基因多态性可能影响日本IgA肾病患者的疾病易感性和疾病进展。《美国肾脏病杂志》41:371-379。