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对伴有猝倒的人类白细胞抗原DQB1*0602阳性发作性睡病患者中前促食欲素原的体液免疫研究。

Studies of humoral immunity to preprohypocretin in human leukocyte antigen DQB1*0602-positive narcoleptic subjects with cataplexy.

作者信息

Black John L, Silber Michael H, Krahn Lois E, Avula Rajeswari K, Walker Denise L, Pankratz V Shane, Fredrickson Paul A, Slocumb Nancy L

机构信息

Psychogenomics Laboratory, Department of Psychiatry and Psychology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.

出版信息

Biol Psychiatry. 2005 Sep 15;58(6):504-9. doi: 10.1016/j.biopsych.2005.04.026.

Abstract

BACKGROUND

Canine models for narcolepsy have mutations of the hypocretin receptor 2 gene, and preprohypocretin knockout murine lines exhibit narcoleptic-like behaviors. Human narcolepsy with cataplexy is associated with human leukocyte antigen DQB10602 and reduced hypocretin levels in cerebrospinal fluid, suggesting an autoimmune diathesis. We tested the hypothesis that DQB10602-positive narcoleptic subjects with cataplexy have immunoglobulin (Ig)G reactive to human preprohypocretin and its cleavage products.

METHODS

Serum samples of 41 DQB1*0602-positive narcoleptic subjects with cataplexy and 55 control subjects were studied, as were 19 narcoleptic and 13 control samples of cerebrospinal fluid. We tested for IgG reactive to preprohypocretin and its major cleavage products (including hypocretin 1 and 2), using immunoprecipitation assays (IP), immunofluorescence microscopy (IF) of Chinese hamster ovarian cells expressing preprohypocretin, and Western blots.

RESULTS

There was no evidence for IgG reactive to preprohypocretin or its cleavage products in CSF of subjects with narcolepsy as measured by IPs, Western blots, and IF. Although the IP with CSF and the C-terminal peptide showed significant differences by two methods of comparison, the control subjects had higher counts per minute than narcoleptic subjects, which was opposite to our hypothesis.

CONCLUSIONS

The hypothesis that DQB1*0602-positive narcoleptic subjects with cataplexy have IgG reactive to preprohypocretin or its cleavage products was not supported.

摘要

背景

发作性睡病的犬类模型具有下丘脑分泌素受体2基因突变,前蛋白原下丘脑分泌素基因敲除的小鼠品系表现出类似发作性睡病的行为。伴有猝倒的人类发作性睡病与人类白细胞抗原DQB10602以及脑脊液中下丘脑分泌素水平降低有关,提示存在自身免疫素质。我们检验了以下假设:伴有猝倒的DQB10602阳性发作性睡病患者具有与人前蛋白原下丘脑分泌素及其裂解产物发生反应的免疫球蛋白(Ig)G。

方法

研究了41例伴有猝倒的DQB1*0602阳性发作性睡病患者和55例对照者的血清样本,以及19例发作性睡病患者和13例对照者的脑脊液样本。我们使用免疫沉淀试验(IP)、对表达前蛋白原下丘脑分泌素的中国仓鼠卵巢细胞进行免疫荧光显微镜检查(IF)以及蛋白质印迹法,检测了与人前蛋白原下丘脑分泌素及其主要裂解产物(包括下丘脑分泌素1和2)发生反应的IgG。

结果

通过IP、蛋白质印迹法和IF检测,未发现发作性睡病患者脑脊液中存在与人前蛋白原下丘脑分泌素或其裂解产物发生反应的IgG。尽管脑脊液与C末端肽的IP通过两种比较方法显示出显著差异,但对照者的每分钟计数高于发作性睡病患者,这与我们的假设相反。

结论

伴有猝倒的DQB1*0602阳性发作性睡病患者具有与人前蛋白原下丘脑分泌素或其裂解产物发生反应的IgG这一假设未得到支持。

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