Multiple sclerosis-associated IL2RA polymorphism controls GM-CSF production in human TH cells

Hartmann, Felix J.; Khademi, Mohsen; Aram, Jehan; Ammann, Sandra; Kockum, Ingrid; Constantinescu, Cris; Gran, Bruno; Piehl, Fredrik; Olsson, Tomas; Codarri, Laura; Becher, Burkhard

Abstract

© 2014 Macmillan Publishers Limited. All rights reserved. Genome-wide association studies implicate dysregulation of immune mechanisms in the pathogenesis of multiple sclerosis (MS). Particularly, polymorphisms in genes involved in T helper (TH) cell differentiation are associated with risk of developing MS. However, the underlying mechanism by which these risk alleles influence MS susceptibility has remained elusive. Initiation of neuroinflammation in animal models of MS has been shown to be dependent on TH cell-derived granulocyte-macrophage colony-stimulating factor (GM-CSF). We here report association of GM-CSF expression by human TH cells with MS disease severity. GM-CSF is strongly induced by interleukin 2 (IL-2). We show that an MS-associated polymorphism in the IL-2 receptor alpha (IL2RA) gene specifically increases the frequency of GM-CSF-producing TH cells. The IL2RA polymorphism regulates IL-2 responsiveness of naive TH cells and their propensity to develop into GM-CSF-producing memory TH cells. These findings mechanistically link an immunologically relevant genetic risk factor with a functional feature of TH cells in MS.

Citation

Hartmann, F. J., Khademi, M., Aram, J., Ammann, S., Kockum, I., Constantinescu, C., Gran, B., Piehl, F., Olsson, T., Codarri, L., & Becher, B. (2014). Multiple sclerosis-associated IL2RA polymorphism controls GM-CSF production in human TH cells. Nature Communications, 5, Article 5056. https://doi.org/10.1038/ncomms6056

• Journal Article Type: Article
• Acceptance Date: Aug 21, 2014
• Online Publication Date: Oct 3, 2014
• Publication Date: Oct 3, 2014
• Deposit Date: Sep 6, 2017
• Journal: Nature Communications
• Electronic ISSN: 2041-1723
• Publisher: Nature Publishing Group
• Peer Reviewed: Peer Reviewed
• Volume: 5
• Article Number: 5056
• DOI: https://doi.org/10.1038/ncomms6056
• Public URL: https://nottingham-repository.worktribe.com/output/1119344
• Publisher URL: https://www.nature.com/articles/ncomms6056
• PMID: 25278028