Synovial cellular and molecular signatures stratify clinical response to csDMARD therapy and predict radiographic progression in early rheumatoid arthritis patients

Humby, F. et al. (2019) Synovial cellular and molecular signatures stratify clinical response to csDMARD therapy and predict radiographic progression in early rheumatoid arthritis patients. Annals of the Rheumatic Diseases, 78(6), pp. 761-772. (doi: 10.1136/annrheumdis-2018-214539) (PMID:30878974) (PMCID:PMC6579551)

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Abstract

Objectives: To unravel the hierarchy of cellular/molecular pathways in the disease tissue of early, treatment-naïve rheumatoid arthritis (RA) patients and determine their relationship with clinical phenotypes and treatment response/outcomes longitudinally. Methods: 144 consecutive treatment-naïve early RA patients (<12 months symptoms duration) underwent ultrasound-guided synovial biopsy before and 6 months after disease-modifying antirheumatic drug (DMARD) initiation. Synovial biopsies were analysed for cellular (immunohistology) and molecular (NanoString) characteristics and results compared with clinical and imaging outcomes. Differential gene expression analysis and logistic regression were applied to define variables correlating with treatment response and predicting radiographic progression. Results: Cellular and molecular analyses of synovial tissue demonstrated for the first time in early RA the presence of three pathology groups: (1) lympho-myeloid dominated by the presence of B cells in addition to myeloid cells; (2) d iffuse-myeloid with myeloid lineage predominance but poor in B cells nd (3) pauci-immune characterised by scanty immune cells and prevalent stromal cells. Longitudinal correlation of molecular signatures demonstrated that elevation of myeloid- and lymphoid-associated gene expression strongly correlated with disease activity, acute phase reactants and DMARD response at 6 months. Furthermore, elevation of synovial lymphoid-associated genes correlated with autoantibody positivity and elevation of osteoclast-targeting genes predicting radiographic joint damage progression at 12 months. Patients with predominant pauci-immune pathology showed less severe disease activity and radiographic progression. Conclusions: We demonstrate at disease presentation, prior to pathology modulation by therapy, the presence of specific cellular/molecular synovial signatures that delineate disease severity/progression and therapeutic response and may pave the way to more precise definition of RA taxonomy, therapeutic targeting and improved outcomes.

Item Type:Articles
Additional Information:This study was funded by Barts and The London School of Medicine and Dentistry Charity (grant number: 523/819); Arthritis Research UK (http://dx.doi.org/10.13039/501100000341), Experimental Arthritis Treatment Centre Grant n:20; Medical Research Council (http://dx.doi.org/10.13039/501100000265), Pathobiology of Early Arthritis Cohort (PEAC) Grant; Medical Research Council (MRC) and Arthritis Research UK (ARUK) for their joint funding of Maximizing Therapeutic Utility in Rheumatoid Arthritis (MATURA) [grant numbers MR/K015346/1, 20670, respectively].
Keywords:Dmards (synthetic), early rheumatoid arthritis, inflammation, synovitis.
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:McInnes, Professor Iain
Authors: Humby, F., Lewis, M., Ramamoorthi, N., Hackney, J. A., Barnes, M. R., Bombardieri, M., Setiadi, A. F., Kelly, S., Bene, F., DiCicco, M., Riahi, S., Rocher, V., Ng, N., Lazarou, I., Hands, R., van der Heijde, D., Landewé, R. B. M., van der Helm-van Mil, A., Cauli, A., McInnes, I., Buckley, C. D., Choy, E. H., Taylor, P. C., Townsend, M. J., and Pitzalis, C.
College/School:College of Medical Veterinary and Life Sciences > School of Infection & Immunity
Research Centre:College of Medical Veterinary and Life Sciences > School of Infection & Immunity > Centre for Immunobiology
Journal Name:Annals of the Rheumatic Diseases
Publisher:BMJ Publishing Group
ISSN:0003-4967
ISSN (Online):1468-2060
Published Online:16 March 2019
Copyright Holders:Copyright © 2019 The Authors
First Published:First published in Annals of the Rheumatic Diseases 78(6):761-772
Publisher Policy:Reproduced under a Creative Commons License

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