脑炎
等位基因
人类白细胞抗原
免疫学
发病机制
自身免疫性脑炎
疾病
人口
基因座(遗传学)
医学
病因学
等位基因频率
HLA-DRB1型
生物
抗原
遗传学
病理
基因
病毒
环境卫生
作者
Yaqing Shu,Wei Qiu,Junfeng Zheng,Xiaobo Sun,Junping Yin,Xiaoli Yang,Xiaoyang Yue,Chen Chen,Zhihui Deng,Shasha Li,Yu Yang,Fuhua Peng,Zhengqi Lu,Xueqiang Hu,Frank Petersen,Xinhua Yu
标识
DOI:10.1136/jnnp-2018-319714
摘要
Background and objective Aetiology and pathogenesis of anti- N -methyl-D-aspartate receptor (anti-NMDAR) encephalitis, the most common autoimmune encephalitis, is largely unknown. Since an association of the disease with the human leucocyte antigen (HLA) has not been shown so far, we here investigated whether anti-NMDAR encephalitis is associated with the HLA locus. Methods HLA loci of 61 patients with anti-NMDAR encephalitis and 571 healthy controls from the Chinese Han population were genotyped and analysed for this study. Results Our results show that the DRB1*16:02 allele is associated with anti-NMDAR encephalitis (OR 3.416, 95% CI 1.817 to 6.174, p=8.9×10 −5 , p adj =0.021), with a higher allele frequency in patients (14.75%) than in controls (4.82%). This association was found to be independent of tumour formation. Besides disease susceptibility, DRB1*16:02 is also related to the clinical outcome of patients during treatment, where patients with DRB1*16:02 showed a lower therapeutic response to the treatment than patients with other HLA alleles (p=0.033). Bioinformatic analysis using HLA peptide-binding prediction algorithms and computational docking suggested a close relationship between the NR1 subunit of NMDAR and the DRB1*16:02 . Conclusions This study for the first time demonstrates an association between specific HLA class II alleles and anti-NMDAR encephalitis, providing novel insights into the pathomechanism of the disease.
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