Development of a Highly Specific 14-3-3 eta (η) ELISA for Rheumatoid Arthritis
Walter P. Maksymowych1, Désirée van der Heijde2, Robert BM Landewé3, George A. Wells4, Joan M. Bathon5, Clifton O. Bingham III6, Vivian P. Bykerk7, Mikkel Ostergaard8, Hilde B. Hammer9, Maarten Boers10, Paul Peter Tak11, Oliver M. FitzGerald12, Christopher T. Ritchlin13, Dafna Gladman14, Philip Mease15, Dirkjan van Schaardenburg16, Marina Backhaus17, Bernard Combe18, Gianfranco Ferraccioli19, Joel Kooistra20, Russell Hart21, Anthony Marotta22
14-3-3 proteins represent a family of ubiquitously expressed intracellular chaperonins consisting of seven different highly conserved isoforms. In 2007, we reported that the eta (η) isoform was present at significantly higher levels in the synovial fluid and serum of patients with arthritis as compared to healthy subjects. That study relied on the semi-quantitative immunoblot approach using a monospecific rabbit polyclonal antibody. Additionally, we reported that there was a significantly strong correlation between the levels of 14-3-3 eta and matrix metalloproteinases (MMPs), and that extracellular 14-3-3 eta possessed ligand-like activity capable of inducing these degradative enzymes underscoring the possible role 14-3-3 eta plays in the pathogenesis of joint damage in RA. The OMERACT soluble biomarker sub-committee has published validation criteria related to truth, discrimination and feasibility for biomarkers reflecting structural damage.[ 2] The large majority of biomarker assays assessed in RA have not undergone such validation, particularly the key assay performance criteria considered essential prior to clinical validation studies. In this study, we present data related to the development and validation of a quantitative 14-3-3 eta ELISA that has been used to investigate the clinical merits of this protein in RA. Rheumatoid arthritis (RA) is a chronic autoimmune disease that if left untreated results in severe joint destruction leading to impaired physical function and work disability. It is now widely accepted that early identification, assessment of the severity of the disease at presentation, together with an early and effective treatment strategy can significantly improve a patient’s prognosis and workplace function.
Methylation Detection, Antibody-free ChIP, ChIP, DNA Methylation, Methylation Analysis, Bisulfate DNA Conversion
Multi-Label Techniques for Colocalization Studies, Microscopy and Imaging, Spinning Disk Microscopy, Confocal Microscopy, Fluorescence Microscopy