Full Papers
High sensitivity measurement of circulating interferon proteins in systemic lupus erythematosus
Y.-J. Huang1, C.M. Bottomley2, R.T. Maughan3, A. Field4, G.H. Leung5, L. Lightstone6, T.D. Cairns7, T. Turner-Stokes8, M.B. Condon9, J.E. Peters10, M. Botto11, M.C. Pickering12
- Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College, London, UK; and School of Medicine, Chang Gung University, Taoyuan, Taiwan, and Division of Rheumatology, Allergy and Immunology, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
- Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College, London, UK.
- Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College, London, UK.
- Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College, London, UK.
- Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College, London, UK.
- Centre for Inflammatory Disease, Department of immunology and Inflammation, Imperial College, London; and Imperial Lupus Centre, Imperial College Healthcare NHS Trust, London, UK.
- Imperial Lupus Centre, Imperial College Healthcare NHS Trust, London, UK.
- Centre for Inflammatory Disease, Department of immunology and Inflammation, Imperial College, London; and Imperial Lupus Centre, Imperial College Healthcare NHS Trust, London, UK.
- Imperial Lupus Centre, Imperial College Healthcare NHS Trust, London, UK.
- Centre for Inflammatory Disease, Department of immunology and Inflammation, Imperial College, London; and Imperial Lupus Centre, Imperial College Healthcare NHS Trust, London, UK.
- Centre for Inflammatory Disease, Department of immunology and Inflammation, Imperial College, London; and Imperial Lupus Centre, Imperial College Healthcare NHS Trust, London, UK.
- Centre for Inflammatory Disease, Department of immunology and Inflammation, Imperial College, London; and Imperial Lupus Centre, Imperial College Healthcare NHS Trust, London, UK. matthew.pickering@imperial.ac.uk
CER18886
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Received: 01/05/2025
Accepted : 10/09/2025
In Press: 23/12/2025
Abstract
OBJECTIVES:
Increased expression of type I interferon-induced genes is a hallmark of systemic lupus erythematosus (SLE). Measurement of interferon proteins in plasma has been challenging due to their low abundance. Here we utilise a new high sensitivity assay to evaluate levels of interferon proteins in SLE patients.
METHODS:
Seven interferon proteins (type I: IFNα1:IFNα13, IFNα2, IFNβ, IFNω; type II: IFNγ; type III: IFNλ1, IFNλ2:IFNλ3) were measured in 266 SLE patients using the NULISAseq Inflammation Panel 250 (Alamar Biosciences). IFN profiles (normal or high) were determined using the 95th percentile threshold in healthy controls for each IFN protein. Their relationship to disease activity and type I interferon-stimulated gene (ISG) scores was assessed.
RESULTS:
All seven IFN proteins were significantly increased in SLE patients compared to healthy controls and were higher in patients with anti-Sm, anti-Ro and anti-RNP antibodies. IFNα1:IFNα13, IFNα2 and IFNω strongly correlated with the ISG score whereas IFNβ did not. The median levels of IFNα1:IFNα13, IFNα2, IFNω, IFNλ1 and IFNλ2:IFNλ3 progressively increased with disease activity whereas this was not the case for either IFNβ or IFNγ. The most frequent IFN profiles were high type I+III (35%, n=93); normal levels of all IFN proteins (25%, n=67); high type I only (21%, n=56); and high type I+II+III (13%, n=34). The latter associated with serological activity (low complement and high dsDNA antibody titres) and nephritis.
CONCLUSIONS:
Plasma levels of type I IFN proteins (IFNα1: IFNα13, IFNα2 and IFNω but not IFNβ) and type III IFN proteins (IFNλ1, IFNλ2:IFNλ3) were increased in active disease groups and ISG scores recapitulated this. Longitudinal intra-individual measures of these proteins are needed to explore their utility as biomarkers for SLE disease activity.
