Natural anti-FcεRIα autoantibodies isolated from healthy donors and chronic idiopathic urticaria patients reveal a restricted repertoire and autoreactivity on human basophils
Affiliations: [a] Institute of Immunology, Inselspital, CH-3010 Bern, Switzerland | [b] Laboratory of Cellular Biotechnology, Center for Biotechnology UNIL-EPFL, EPFL, CH-1015 Lausanne, Switzerland | [c] ZLB Bioplasma, Wankdorfstrasse 10, CH-3014 Bern, Switzerland
Correspondence:
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Corresponding author: Sylvia M. Miescher, Ph D, Institute of Immunology, Sahlihaus 1, Inselspital, CH-3010 Bern, Switzerland. E-mail: sylvia.miescher@insel.ch.
Note: [**] Current address: Institute of Virology and Immunoprophylaxis, Sensemattstr 293, 3147 Mittelhäusern, Switzerland.
Abstract: The role of autoantibodies against the α-subunit of the human high-affinity IgE receptor (FcεRIα) in the pathogenesis of chronic idiopathic urticaria (CIU) is controversial. We have shown that these antibodies are widespread, apparently non-pathogenic and belong to the natural antibody repertoire. To clarify this controversy, we constructed antibody libraries from both healthy donors and CIU patients with active disease. Here we describe the first three high affinity IgM anti-FcεRIαautoantibodies isolated from normal and urticaria libraries. Sequence analysis revealed germline VH in both cases paired with a slightly mutated VL, thus supporting their classification as natural antibodies. Strikingly, one major IgM clone was present in both CIU patients and normal donors. The anti-FcεRIα autoantibodies recognize FcεRIα on cells, but are non-anaphylactogenic on blood basophils, except when IgE is removed from the receptor. Based on their functional activities we propose a concept of “conditional autoimmunity” where natural anti-FcεRIαautoantibodies can become pathogenic dependent on the state of occupancy of the FcεRIα by its natural ligand IgE.
