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

Author

Listed:
  • Daniela Latorre

    (Università della Svizzera italiana
    Institute of Microbiology, ETH Zurich)

  • Ulf Kallweit

    (University Hospital
    University of Witten/Herdecke)

  • Eric Armentani

    (Università della Svizzera italiana)

  • Mathilde Foglierini

    (Università della Svizzera italiana
    Swiss Institute of Bioinformatics)

  • Federico Mele

    (Università della Svizzera italiana)

  • Antonino Cassotta

    (Università della Svizzera italiana
    Institute of Microbiology, ETH Zurich)

  • Sandra Jovic

    (Università della Svizzera italiana)

  • David Jarrossay

    (Università della Svizzera italiana)

  • Johannes Mathis

    (University Hospital)

  • Francesco Zellini

    (Neurocenter of Southern Switzerland)

  • Burkhard Becher

    (University of Zurich)

  • Antonio Lanzavecchia

    (Università della Svizzera italiana)

  • Ramin Khatami

    (Clinic Barmelweid)

  • Mauro Manconi

    (University Hospital
    Neurocenter of Southern Switzerland)

  • Mehdi Tafti

    (Faculty of Biology and Medicine, University of Lausanne)

  • Claudio L. Bassetti

    (University Hospital)

  • Federica Sallusto

    (Università della Svizzera italiana
    Institute of Microbiology, ETH Zurich)

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+ 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+ T cells were polyclonal, targeted multiple epitopes, were restricted primarily by HLA-DR and did not cross-react with influenza antigens. Hypocretin-specific CD8+ 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.

Suggested Citation

  • Daniela Latorre & Ulf Kallweit & Eric Armentani & Mathilde Foglierini & Federico Mele & Antonino Cassotta & Sandra Jovic & David Jarrossay & Johannes Mathis & Francesco Zellini & Burkhard Becher & Ant, 2018. "T cells in patients with narcolepsy target self-antigens of hypocretin neurons," Nature, Nature, vol. 562(7725), pages 63-68, October.
  • Handle: RePEc:nat:nature:v:562:y:2018:i:7725:d:10.1038_s41586-018-0540-1
    DOI: 10.1038/s41586-018-0540-1
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    Citations

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    Cited by:

    1. Hao Hu & Anthony N. Vomund & Orion J. Peterson & Neetu Srivastava & Tiandao Li & Lisa Kain & Wandy L. Beatty & Bo Zhang & Chyi-Song Hsieh & Luc Teyton & Cheryl F. Lichti & Emil R. Unanue & Xiaoxiao Wa, 2024. "Crinophagic granules in pancreatic β cells contribute to mouse autoimmune diabetes by diversifying pathogenic epitope repertoire," Nature Communications, Nature, vol. 15(1), pages 1-22, December.
    2. Hanna M. Ollila & Eilon Sharon & Ling Lin & Nasa Sinnott-Armstrong & Aditya Ambati & Selina M. Yogeshwar & Ryan P. Hillary & Otto Jolanki & Juliette Faraco & Mali Einen & Guo Luo & Jing Zhang & Fang H, 2023. "Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    3. Hideki Ogura & Jin Gohda & Xiuyuan Lu & Mizuki Yamamoto & Yoshio Takesue & Aoi Son & Sadayuki Doi & Kazuyuki Matsushita & Fumitaka Isobe & Yoshihiro Fukuda & Tai-Ping Huang & Takamasa Ueno & Naomi Mam, 2022. "Dysfunctional Sars-CoV-2-M protein-specific cytotoxic T lymphocytes in patients recovering from severe COVID-19," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

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