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CD8(+) T cells from patients with narcolepsy and healthy controls recognize hypocretin neuron-specific antigens

Narcolepsy Type 1 (NT1) is a neurological sleep disorder, characterized by the loss of hypocretin/orexin signaling in the brain. Genetic, epidemiological and experimental data support the hypothesis that NT1 is a T-cell-mediated autoimmune disease targeting the hypocretin producing neurons. While au...

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Detalles Bibliográficos
Autores principales: Pedersen, Natasja Wulff, Holm, Anja, Kristensen, Nikolaj Pagh, Bjerregaard, Anne-Mette, Bentzen, Amalie Kai, Marquard, Andrea Marion, Tamhane, Tripti, Burgdorf, Kristoffer Sølvsten, Ullum, Henrik, Jennum, Poul, Knudsen, Stine, Hadrup, Sine Reker, Kornum, Birgitte Rahbek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381094/
https://www.ncbi.nlm.nih.gov/pubmed/30783092
http://dx.doi.org/10.1038/s41467-019-08774-1
Descripción
Sumario:Narcolepsy Type 1 (NT1) is a neurological sleep disorder, characterized by the loss of hypocretin/orexin signaling in the brain. Genetic, epidemiological and experimental data support the hypothesis that NT1 is a T-cell-mediated autoimmune disease targeting the hypocretin producing neurons. While autoreactive CD4(+) T cells have been detected in patients, CD8(+) T cells have only been examined to a minor extent. Here we detect CD8(+) T cells specific toward narcolepsy-relevant peptides presented primarily by NT1-associated HLA types in the blood of 20 patients with NT1 as well as in 52 healthy controls, using peptide-MHC-I multimers labeled with DNA barcodes. In healthy controls carrying the disease-predisposing HLA-DQB1*06:02 allele, the frequency of autoreactive CD8(+) T cells was lower as compared with both NT1 patients and HLA-DQB1*06:02-negative healthy individuals. These findings suggest that a certain level of CD8(+) T-cell reactivity combined with HLA-DQB1*06:02 expression is important for NT1 development.