Xu Ricong, Li Qibin, Liu Rongjun, Shen Juan, Li Ming, Zhao Minghui, Wang Meng, Liao Qijun, Mao Haiping, Li Zhijian, Zhou Na, Yin Peiran, Li Yue, Tang Xueqing, Wu Tian, Zhong Zhong, Wang Yan, Ai Zhen, Wang Ou, Chen Nan, Yang Xiaoqin, Fang Junbin, Fu Ping, Gu Jieruo, Ye Kun, Chen Jian, Dai Lie, Liu Huafeng, Liu Zhangsuo, Liao Yunhua, Wan Jianxin, Ding Guohua, Zhao Jinghong, Zhang Hao, Fu Shuxia, Sun Liangdan, Zhang Xuejun, Yang Huanming, Wang Jian, Wang Jun, Liu Jianjun, Li Yingrui, Yu Xueqing
Department of Nephrology, The First Affiliated Hospital, Sun Yat-sen University, Key Laboratory of Nephrology, Ministry of Health, Guangzhou, Guangdong, China.
Department of Nephrology, Shenzhen Second People's Hospital and the First Affiliated Hospital of Shenzhen University, Shenzhen, China.
J Am Soc Nephrol. 2017 Nov;28(11):3383-3394. doi: 10.1681/ASN.2016121331. Epub 2017 Jul 28.
Lupus nephritis (LN) is one of the most prevalent and serious complications of SLE, with significant effects on patient and renal survival. Although a large number of genetic variants associated with SLE have been identified, biomarkers that correlate with LN are extremely limited. In this study, we performed a comprehensive sequencing analysis of the whole MHC region in 1331 patients with LN and 1296 healthy controls and validated the independent associations in another 950 patients with LN and 1000 controls. We discovered five independent risk variants for LN within the MHC region, including amino acid 11 (<0.001), amino acid 45 (<0.001; odds ratio, 0.58; 95% confidence interval, 0.52 to 0.65), amino acid 156 (<0.001), amino acid 76 (<0.001), and a missense variant in (rs114580964; <0.001; odds ratio, 0.38; 95% confidence interval, 0.30 to 0.49) at genome-wide significance. These data implicate aberrant peptide presentation by MHC classes 1 and 2 molecules and sex hormone modulation in the development of LN.
狼疮性肾炎(LN)是系统性红斑狼疮(SLE)最常见且最严重的并发症之一,对患者和肾脏存活率有重大影响。尽管已鉴定出大量与SLE相关的基因变异,但与LN相关的生物标志物极其有限。在本研究中,我们对1331例LN患者和1296例健康对照的整个主要组织相容性复合体(MHC)区域进行了全面测序分析,并在另外950例LN患者和1000例对照中验证了独立关联。我们在MHC区域内发现了五个LN的独立风险变异,包括第11位氨基酸(<0.001)、第45位氨基酸(<0.001;比值比,0.58;95%置信区间,0.52至0.65)、第156位氨基酸(<0.001)、第76位氨基酸(<0.001),以及在全基因组显著性水平下位于[具体基因名称未给出]的一个错义变异(rs114580964;<0.001;比值比,0.38;95%置信区间,0.30至0.49)。这些数据表明,MHC Ⅰ类和Ⅱ类分子异常的肽呈递以及性激素调节在LN的发生发展中起作用。