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发作性睡病中针对下丘脑分泌素、hcrtrl和hcrtr2自身抗体的检测:发作性睡病中的抗下丘脑分泌素系统抗体。

Detection of autoantibodies against hypocretin, hcrtrl, and hcrtr2 in narcolepsy: anti-Hcrt system antibody in narcolepsy.

作者信息

Tanaka Susumu, Honda Yutaka, Inoue Yuichi, Honda Makoto

机构信息

The Sleep Disorders Project, Department of Sleep Disorders Research, Tokyo Institute of Psychiatry, Setagaya-ku, Tokyo, Japan.

出版信息

Sleep. 2006 May;29(5):633-8. doi: 10.1093/sleep/29.5.633.

DOI:10.1093/sleep/29.5.633
PMID:16774153
Abstract

STUDY OBJECTIVES

The impairment of hypocretin neurotransmission system is considered to play a major role in the pathophysiology of narcolepsy. It has been hypothesized that autoimmune abnormalities underlie the etiology of narcolepsy, based on the tight association with HLA-DRB11501/ DQB10602. It remains unclear if autoantibodies against hypocretin receptors (hcrtrl and hcrtr2) are involved in narcolepsy.

DESIGN

We have developed a novel radioligand binding assay to address this question. Sera from 181 patients with narcolepsy, 10 patients with other hypersomnias, and 91 control subjects were used. Human [35S]-Hcrt, hcrtrl, and hcrtr2 were synthesized by in vitro transcription/translation system. The immune complex of autoantibody and each [35S]-protein were immunoprecipitated and quantified using a radioligand-binding assay.

RESULTS

We detected autoantibodies against hypocretin in 3 patients, hcrtrl in 1 patient, and hcrtr2 in 5 patients with narcolepsy. Positive reactions were also found against hcrtrl in 2 and hcrtr2 in 1 control subjects. No relationships were found between these autoantibodies and HLA-DRB11501/DQB10602 haplotypes, presence of cataplexy, presence of subjective nocturnal sleep disruption, or the score on the Epworth Sleepiness Scale.

CONCLUSIONS

Although we have detected autoantibodies against the hypocretin neurotransmission system, our results do not support the hypothesis that autoantibody-mediated dysfunction in the hypocretin system underlies the pathophysiology of narcolepsy.

摘要

研究目的

下丘脑分泌素神经传递系统的损害被认为在发作性睡病的病理生理学中起主要作用。基于与HLA - DRB11501/DQB10602的紧密关联,有人提出自身免疫异常是发作性睡病病因的基础。目前尚不清楚针对下丘脑分泌素受体(hcrtrl和hcrtr2)的自身抗体是否参与发作性睡病。

设计

我们开发了一种新型放射性配体结合测定法来解决这个问题。使用了181例发作性睡病患者、10例其他发作性睡病患者和91例对照受试者的血清。通过体外转录/翻译系统合成人[35S]-下丘脑分泌素、hcrtrl和hcrtr2。自身抗体与每种[35S]蛋白的免疫复合物通过放射性配体结合测定法进行免疫沉淀和定量。

结果

我们在3例发作性睡病患者中检测到针对下丘脑分泌素的自身抗体,1例患者中检测到针对hcrtrl的自身抗体,5例患者中检测到针对hcrtr2的自身抗体。在2例对照受试者中也发现了针对hcrtrl的阳性反应,1例对照受试者中发现了针对hcrtr2的阳性反应。这些自身抗体与HLA - DRB11501/DQB10602单倍型、猝倒的存在、主观夜间睡眠中断的存在或爱泼华嗜睡量表评分之间均未发现关联。

结论

虽然我们检测到了针对下丘脑分泌素神经传递系统的自身抗体,但我们的结果不支持自身抗体介导的下丘脑分泌素系统功能障碍是发作性睡病病理生理学基础这一假说。

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