Author:
Tesch Sebastian,Abdirama Dimas,Grießbach Anna-Sophie,Brand Hannah Antonia,Goerlich Nina,Humrich Jens Y.,Bacher Petra,Hiepe Falk,Riemekasten Gabriela,Enghard Philipp
Abstract
AbstractIn the search for anti-renal autoreactivity in human lupus nephritis, we stimulated blood-derived CD4+ T cells from patients with systemic lupus erythematosus with various kidney lysates. Although only minor responses were detectable, these experiments led to the development of a search algorithm that combined autoantibody association with human lupus nephritis and target gene expression in inflamed kidneys. Applying this algorithm, five potential T cell antigens were identified. Blood-derived CD4+ T cells were then stimulated with these antigens. The cells were magnetically enriched prior to measurement with flow cytometry to facilitate the detection of very rare autoantigen-specific cells. The detected responses were dominated by IFN-γ-producing CD4+ T cells. Additionally, IL-10-producing CD4+ T cells were found. In a next step, T cell reactivity to each single antigen was independently evaluated with T cell libraries and [3H]-thymidine incorporation assays. Here, Vimentin and Annexin A2 were identified as the main T cell targets. Finally, Vimentin reactive T cells were also found in the urine of three patients with active disease. Overall, our experiments show that antigen-specific CD4+ T cells targeting renally expressed antigens arise in human lupus nephritis and correlate with disease activity and are mainly of the Th1 subset.
Funder
German Society of Nephrology
Clinical scientist program of the Charité University Hospital Berlin and the Berlin Institute of Health
Projekt DEAL
Publisher
Springer Science and Business Media LLC
Cited by
10 articles.
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