Author/Authors :
Lindop، نويسنده , , Rhianna and Arentz، نويسنده , , Georgia and Bastian، نويسنده , , Isabell and Whyte، نويسنده , , Andrew F. and Thurgood، نويسنده , , Lauren A. and Chataway، نويسنده , , Tim K. and Jackson، نويسنده , , Michael W. and Gordon، نويسنده , , Tom P.، نويسنده ,
Abstract :
Long-term humoral autoimmunity to RNA–protein autoantigens is considered a hallmark of systemic autoimmune diseases. We use high resolution Orbitrap mass spectrometric autoantibody sequencing to track the evolution of a Ro60-specific public clonotypic autoantibody in 4 patients with primary Sjögrenʹs syndrome. This clonotype is specified by a VH3–23/VK3–20 heavy and light chain pairing. Despite apparent stability by conventional immunoassay, analysis of V-region molecular signatures of clonotypes purified from serum samples collected retrospectively over 7 years revealed sequential clonal replacement. Prospective longitudinal studies confirmed clonotype loss and replacement at approximately three-monthly intervals. Levels of secreted anti-Ro60 clonotypes fluctuated markedly over time, despite minimal changes in clonal affinity. Our novel findings indicate a relentless turnover of short-lived clonotypic variants, masquerading as long-lived Ro60 humoral autoimmunity.
Keywords :
Ro60 , Humoral autoimmunity , mass spectrometry , autoantibodies , primary Sjِgrenיs syndrome