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S Meyer, M Woodward, C Hertel, P Vlaicu, Y Haque, J Kärner, A Macagno, SC Onuoha, D Fishman, H Peterson, K Metsküla, R Uibo, K Jäntti, K Hokynar, AS Wolff, K Krohn, A Ranki, P Peterson, K Kisand and A Hayday
Abstract
APS1/APECED patients are defined by defects in the autoimmune regulator (AIRE) that mediates central T cell tolerance to many self-antigens. AIRE deficiency also affects B cell tolerance, but this is incompletely understood. Here we show that most APS1/APECED patients displayed B cell autoreactivity toward unique sets of approximately 100 self-proteins. Thereby, autoantibodies from 81 patients collectively detected many thousands of human proteins. The loss of B cell tolerance seemingly occurred during antibody affinity maturation, an obligatorily T cell-dependent step. Consistent with this, many APS1/APECED patients harbored extremely high-affinity, neutralizing autoantibodies, particularly against specific cytokines. Such antibodies were biologically active in vitro and in vivo, and those neutralizing type I interferons (IFNs) showed a striking inverse correlation with type I diabetes, not shown by other anti-cytokine antibodies. Thus, naturally occurring human autoantibodies may actively limit disease and be of therapeutic utility.
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Concepts
Interferon, Somatic hypermutation, Immunology, Cytokine, Diabetes mellitus type 1, Protein, Antibody, Immune system
MeSH headings
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