TY - JOUR
T1 - Identification and characterization of antigen-specific CD4+ T cells targeting renally expressed antigens in human lupus nephritis with two independent methods
AU - Tesch, Sebastian
AU - Abdirama, Dimas
AU - Grießbach, Anna Sophie
AU - Brand, Hannah Antonia
AU - Goerlich, Nina
AU - Humrich, Jens Y.
AU - Bacher, Petra
AU - Hiepe, Falk
AU - Riemekasten, Gabriela
AU - Enghard, Philipp
N1 - Funding Information:
The results and figures of the experiments with kidney lysates are based on data that A-S.G. has published online as an MD thesis75. The authors would like to thank the FCCF at the DRFZ for assistance with flow cytometry. We thank all patients and healthy donors who provided samples. This study was funded by grants from the German Society of Nephrology, the German Research Foundation (DFG) and the clinical scientist program of the Charité University Hospital Berlin and the Berlin Institute of Health to PE. S.T., A-S.G. and H.A.B were supported by the Leibniz Graduate School for Rheumatology (LGRh).
Publisher Copyright:
© 2020, The Author(s).
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/12
Y1 - 2020/12
N2 - In 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.
AB - In 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.
UR - http://www.scopus.com/inward/record.url?scp=85097093285&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/cd3a143d-cff8-3457-a8ed-21c9d49450cf/
U2 - 10.1038/s41598-020-78223-3
DO - 10.1038/s41598-020-78223-3
M3 - Journal articles
C2 - 33277543
AN - SCOPUS:85097093285
SN - 2045-2322
VL - 10
SP - 21312
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 21312
ER -