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HLA class II allele DRB1*16:02is associated with anti-NMDAR encephalitis

Authors :
Shu, Yaqing
Qiu, Wei
Zheng, Junfeng
Sun, Xiaobo
Yin, Junping
Yang, Xiaoli
Yue, Xiaoyang
Chen, Chen
Deng, Zhihui
Li, Shasha
Yang, Yu
Peng, Fuhua
Lu, Zhengqi
Hu, Xueqiang
Petersen, Frank
Yu, Xinhua
Source :
Journal of Neurology, Neurosurgery, & Psychiatry (JNNP); 2019, Vol. 90 Issue: 6 p652-658, 7p
Publication Year :
2019

Abstract

Background and objectiveAetiology 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.MethodsHLA loci of 61 patients with anti-NMDAR encephalitis and 571 healthy controls from the Chinese Han population were genotyped and analysed for this study.ResultsOur results show that the DRB1*16:02allele is associated with anti-NMDAR encephalitis (OR 3.416, 95% CI 1.817 to 6.174, p=8.9×10−5, padj=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*16:02is also related to the clinical outcome of patients during treatment, where patients with DRB1*16:02showed 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.ConclusionsThis 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.

Details

Language :
English
ISSN :
00223050 and 1468330X
Volume :
90
Issue :
6
Database :
Supplemental Index
Journal :
Journal of Neurology, Neurosurgery, & Psychiatry (JNNP)
Publication Type :
Periodical
Accession number :
ejs50081342
Full Text :
https://doi.org/10.1136/jnnp-2018-319714