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Different antibody-associated autoimmune diseases have distinct patterns of T follicular cell dysregulation

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  • Additional Information
    • Publication Information:
      Springer Nature
    • Publication Date:
      2022
    • Collection:
      Universidade de Lisboa: repositório.UL
    • Abstract:
      © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. ; Autoantibodies are produced within germinal centers (GC), in a process regulated by interactions between B, T follicular helper (Tfh), and T follicular regulatory (Tfr) cells. The GC dysregulation in human autoimmunity has been inferred from circulating cells, albeit with conflicting results due to diverse experimental approaches. We applied a consistent approach to compare circulating Tfr and Tfh subsets in patients with different autoimmune diseases. We recruited 97 participants, including 72 patients with Hashimoto's thyroiditis (HT, n = 18), rheumatoid arthritis (RA, n = 16), or systemic lupus erythematosus (SLE, n = 32), and 31 matched healthy donors (HD). We found that the frequency of circulating T follicular subsets differed across diseases. Patients with HT had an increased frequency of blood Tfh cells (p = 0.0215) and a reduced Tfr/Tfh ratio (p = 0.0338) when compared with HD. This was not observed in patients with systemic autoimmune rheumatic diseases (RA, SLE), who had a reduction in both Tfh (p = 0.0494 and p = 0.0392, respectively) and Tfr (p = 0.0003 and p = 0.0001, respectively) cells, resulting in an unchanged Tfr/Tfh ratio. Activated ...
    • ISSN:
      2045-2322
    • Relation:
      EJPRD/0003/2019; https://www.nature.com/srep/; Sci Rep. 2022 Oct 21;12(1):17638; http://hdl.handle.net/10451/54926
    • Accession Number:
      10.1038/s41598-022-21576-8
    • Online Access:
      http://hdl.handle.net/10451/54926
      https://doi.org/10.1038/s41598-022-21576-8
    • Rights:
      openAccess ; http://creativecommons.org/licenses/by/4.0/
    • Accession Number:
      edsbas.6A2760FF