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T cells in patients with narcolepsy target self-antigens of hypocretin neurons

Authors :
Latorre, Daniela
Kallweit, Ulf
Armentani, Eric
Foglierini, Mathilde
Mele, Federico
Cassotta, Antonino
Jovic, Sandra
Source :
Nature. October, 2018, Vol. 562 Issue 7725, p63, 6 p.
Publication Year :
2018

Abstract

Narcolepsy is a chronic sleep disorder caused by the loss of neurons that produce hypocretin. The close association with HLA-DQB1*06:02, evidence for immune dysregulation and increased incidence upon influenza vaccination together suggest that this disorder has an autoimmune origin. However, there is little evidence of autoreactive lymphocytes in patients with narcolepsy. Here we used sensitive cellular screens and detected hypocretin-specific CD4.sup.+ T cells in all 19 patients that we tested; T cells specific for tribbles homologue 2--another self-antigen of hypocretin neurons--were found in 8 out of 13 patients. Autoreactive CD4.sup.+ T cells were polyclonal, targeted multiple epitopes, were restricted primarily by HLA-DR and did not cross-react with influenza antigens. Hypocretin-specific CD8.sup.+ T cells were also detected in the blood and cerebrospinal fluid of several patients with narcolepsy. Autoreactive clonotypes were serially detected in the blood of the same--and even of different--patients, but not in healthy control individuals. These findings solidify the autoimmune aetiology of narcolepsy and provide a basis for rapid diagnosis and treatment of this disease.The detection of hypocretin-specific autoreactive CD4.sup.+ and CD8.sup.+ T cells in patients with narcolepsy reveals the autoimmune aetiology of this disorder.<br />Author(s): Daniela Latorre [sup.1] [sup.2] , Ulf Kallweit [sup.3] [sup.4] , Eric Armentani [sup.1] , Mathilde Foglierini [sup.1] [sup.5] , Federico Mele [sup.1] , Antonino Cassotta [sup.1] [sup.2] , Sandra [...]

Details

Language :
English
ISSN :
00280836
Volume :
562
Issue :
7725
Database :
Gale General OneFile
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
edsgcl.572996396
Full Text :
https://doi.org/10.1038/s41586-018-0540-1