| Literature DB >> 32592813 |
Dimas Abdirama1, Sebastian Tesch1, Anna-Sophie Grießbach1, Caroline von Spee-Mayer2, Jens Y Humrich3, Ulrik Stervbo4, Nina Babel4, Christian Meisel5, Tobias Alexander6, Robert Biesen6, Petra Bacher1, Alexander Scheffold1, Kai-Uwe Eckardt7, Falk Hiepe6, Andreas Radbruch8, Gerd-Rüdiger Burmester6, Gabriela Riemekasten9, Philipp Enghard10.
Abstract
Systemic lupus erythematosus is a systemic and chronic autoimmune disease characterized by loss of tolerance towards nuclear antigens with autoreactive CD4+ T cells implicated in disease pathogenesis. However, very little is known about their receptor specificity since the detection of human autoantigen specific CD4+ T cells has been extremely challenging. Here we present an analysis of CD4+ T cells reactive to nuclear antigens using two complementary methods: T cell libraries and antigen-reactive T cell enrichment. The frequencies of nuclear antigen specific CD4+ T cells correlated with disease severity. These autoreactive T cells produce effector cytokines such as interferon-γ, interleukin-17, and interleukin-10. Compared to blood, these cells were enriched in the urine of patients with active lupus nephritis, suggesting an infiltration of the inflamed kidneys. Thus, these previously unrecognized characteristics support a role for nuclear antigen-specific CD4+ T cells in systemic lupus erythematosus.Entities:
Keywords: SLE; autoreactive T cells; lupus nephritis
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Year: 2020 PMID: 32592813 DOI: 10.1016/j.kint.2020.05.051
Source DB: PubMed Journal: Kidney Int ISSN: 0085-2538 Impact factor: 10.612