The autoimmune basis of narcolepsy.

The autoimmune basis of narcolepsy.
复制标题

DOI:
10.1016/j.conb.2013.04.013
复制
发表时间:
2013-10
影响因子:
5.7
通讯作者:
Mignot E
Mignot E
中科院分区:
医学2区
文献类型:
--
作者:
Mahlios J;De la Herrán-Arita AK;Mignot E

文献摘要

参考文献

被引文献

相似文献

Narcolepsy is a neurological disorder characterized by excessive daytime sleepiness, cataplexy, hypnagonic hallucinations, sleep paralysis, and disturbed nocturnal sleep patterns. Narcolepsy is caused by the loss of hypocretin (orexin)-producing neurons in the lateral hypothalamus. Evidence, such as a strong association with HLA DQB1*06:02, strongly suggests an autoimmune basis targeting hypocretin neurons. Genome-wide association studies have strengthened the association between narcolepsy and immune system gene polymorphisms, including the identification of polymorphisms in the T cell receptor alpha locus, TNFSF4 (also called OX40L), Cathepsin H (CTSH) the purinergic receptor P2RY11, and the DNA methyltransferase DNMT1. Recently, attention has been raised regarding a spike in cases of childhood narcolepsy in 2010 following the 2009 H1N1 pandemic (pH1N1) in China and vaccination with Pandemrix, an adjuvanted H1N1 vaccine that was used in Europe. How the immune system may be involved in disease initiation and/or progression remains a challenge to researchers. Potential immunological pathways that could lead to the specific elimination of hypocretin producing neurons include molecular mimicry or bystander activation, and are likely a combination of genetic and environmental factors, such as upper airway infections.
DOI: 10.1371/journal.pgen.1003270
发表时间: 2013
期刊: PLoS genetics
影响因子: 4.5
作者:
Faraco J;Lin L;Kornum BR;Kenny EE;Trynka G;Einen M;Rico TJ;Lichtner P;Dauvilliers Y;Arnulf I;Lecendreux M;Javidi S;Geisler P;Mayer G;Pizza F;Poli F;Plazzi G;Overeem S;Lammers GJ;Kemlink D;Sonka K;Nevsimalova S;Rouleau G;Desautels A;Montplaisir J;Frauscher B;Ehrmann L;Högl B;Jennum P;Bourgin P;Peraita-Adrados R;Iranzo A;Bassetti C;Chen WM;Concannon P;Thompson SD;Damotte V;Fontaine B;Breban M;Gieger C;Klopp N;Deloukas P;Wijmenga C;Hallmayer J;Onengut-Gumuscu S;Rich SS;Winkelmann J;Mignot E
通讯作者: Mignot E
DOI: 10.1371/journal.pone.0013320
发表时间: 2010-10-13
期刊: PloS one
影响因子: 3.7
作者:
Deloumeau A;Bayard S;Coquerel Q;Déchelotte P;Bole-Feysot C;Carlander B;Cochen De Cock V;Fetissov SO;Dauvilliers Y
通讯作者: Dauvilliers Y
DOI: 10.1038/ng.372
发表时间: 2009-06-01
期刊: NATURE GENETICS
影响因子: 30.8
作者:
Hallmayer, Joachim;Faraco, Juliette;Mignot, Emmanuel
通讯作者: Mignot, Emmanuel
DOI: 10.1016/s0092-8674(00)81965-0
发表时间: 1999-08-06
期刊: CELL
影响因子: 64.5
作者:
Lin, L;Faraco, J;Mignot, E
通讯作者: Mignot, E
DOI: 10.1002/ana.22587
发表时间: 2011-09-01
影响因子: 11.2
作者:
Han, Fang;Lin, Ling;Mignot, Emmanuel
通讯作者: Mignot, Emmanuel