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

被引:28
作者
Black, JL
Silber, MH
Krahn, LE
Avula, RK
Walker, DL
Pankratz, VS
Fredrickson, PA
Slocumb, NL
机构
[1] Mayo Clin, Coll Med, Dept Psychiat & Psychol, Psychogenom Lab, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Neurol, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN 55905 USA
[4] Mayo Clin, Coll Med, Mayo Sleep Disorders Ctr, Rochester, MN 55905 USA
[5] Mayo Clin, Coll Med, Dept Psychiat & Psychol, Scottsdale, AZ USA
[6] Mayo Clin, Coll Med, Mayo Sleep Disorders Lab, Scottsdale, AZ USA
[7] Mayo Clin, Coll Med, Dept Psychiat & Psychol, Jacksonville, FL USA
[8] Mayo Clin, Coll Med, Mayo Sleep Disorders Lab, Jacksonville, FL USA
关键词
narcolepsy; autoimmunity; hypocretin; orexin; immunoglobulin G; DQB1*0602;
D O I
10.1016/j.biopsych.2005.04.026
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Canine models for narcolepsy have mutations of the hypocretin receptor 2 gene, and preprohypocretin knockout murine V lines exhibit narcoleptic-like behaviors. Human narcolepsy with cataplexy is associated with human leukocyte antigen DQB1*0602 and reduced hypocretin levels in cerebrospinal fluid, suggesting an autoimmune diathesis. We tested the hypothesis that DQB1*0602-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 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 bad 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.
引用
收藏
页码:504 / 509
页数:6
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