IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v488y2012i7412d10.1038_nature11307.html
   My bibliography  Save this article

TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis

Author

Listed:
  • Adam P. Gregory

    (MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Calliope A. Dendrou

    (John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Kathrine E. Attfield

    (John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Aiden Haghikia

    (John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK
    St. Josef-Hospital Bochum, Ruhr-University Bochum, 44791 Bochum, Germany)

  • Dionysia K. Xifara

    (Wellcome Trust Centre for Human Genetics, Roosevelt Drive, University of Oxford, Oxford OX3 7BN, UK)

  • Falk Butter

    (Max-Planck-Institute of Biochemistry, D-82152 Martinsried, Germany)

  • Gereon Poschmann

    (Molecular Proteomics Laboratory, Biologisch-Medizinisches Forschungszentrum, Heinrich-Heine Universität Düsseldorf, D-40225 Düsseldorf, Germany)

  • Gurman Kaur

    (MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Lydia Lambert

    (John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Oliver A. Leach

    (John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Simone Prömel

    (John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Divya Punwani

    (MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • James H. Felce

    (MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Simon J. Davis

    (MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK)

  • Ralf Gold

    (St. Josef-Hospital Bochum, Ruhr-University Bochum, 44791 Bochum, Germany)

  • Finn C. Nielsen

    (Center for Genomic Medicine, Rigshospitalet, University of Copenhagen, DK-2100 Copenhagen Ø, Denmark)

  • Richard M. Siegel

    (Immunoregulation Section, Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases/NIH, 10 Center Drive)

  • Matthias Mann

    (Max-Planck-Institute of Biochemistry, D-82152 Martinsried, Germany)

  • John I. Bell

    (Richard Doll Building, Roosevelt Drive, University of Oxford, Oxford OX3 7DG, UK)

  • Gil McVean

    (Wellcome Trust Centre for Human Genetics, Roosevelt Drive, University of Oxford, Oxford OX3 7BN, UK)

  • Lars Fugger

    (MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK
    John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, UK
    Clinical Institute, Aarhus University Hospital, Skejby Sygehus, 8200 N Aarhus, Denmark)

Abstract

Genome-wide association studies in combination with functional analyses identify a genetic variant that explains why anti-tumour necrosis factor therapy, used in several autoimmune diseases, exacerbates multiple sclerosis.

Suggested Citation

  • Adam P. Gregory & Calliope A. Dendrou & Kathrine E. Attfield & Aiden Haghikia & Dionysia K. Xifara & Falk Butter & Gereon Poschmann & Gurman Kaur & Lydia Lambert & Oliver A. Leach & Simone Prömel & Di, 2012. "TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis," Nature, Nature, vol. 488(7412), pages 508-511, August.
  • Handle: RePEc:nat:nature:v:488:y:2012:i:7412:d:10.1038_nature11307
    DOI: 10.1038/nature11307
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature11307
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature11307?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Kensuke Yamaguchi & Kazuyoshi Ishigaki & Akari Suzuki & Yumi Tsuchida & Haruka Tsuchiya & Shuji Sumitomo & Yasuo Nagafuchi & Fuyuki Miya & Tatsuhiko Tsunoda & Hirofumi Shoda & Keishi Fujio & Kazuhiko , 2022. "Splicing QTL analysis focusing on coding sequences reveals mechanisms for disease susceptibility loci," Nature Communications, Nature, vol. 13(1), pages 1-13, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:488:y:2012:i:7412:d:10.1038_nature11307. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.