4.8 Article

CD11c+ B Cells Participate in the Pathogenesis of Graves' Disease by Secreting Thyroid Autoantibodies and Cytokines

Journal

FRONTIERS IN IMMUNOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.836347

Keywords

CD11c(+) B cells; TRAb; Graves' disease; cytokines; CXCR3-CXCL10

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Funding

  1. National Natural Science Foundation of China [81770783, 82170801]

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In this study, CD11c(+) B cells were found to be expanded in the peripheral blood of GD patients, and their frequency was positively correlated with serum TRAb levels. CD11c(+) B cells were also observed in the lymphocyte infiltration areas of the GD thyroid. CD11c(+) B cells from the peripheral blood of GD patients were induced to differentiate into autoreactive antibody-secreting cells capable of secreting TRAbs. CD11c(+) B cells also secreted various cytokines and were recruited by thyroid follicular cells via the CXCR3-CXCL10 axis.
Graves' disease (GD) is a common autoimmune disorder with an elevation in pathogenic autoantibodies, specifically anti-thyrotropin receptor antibodies (TRAbs), which are secreted by autoreactive B cells. To date, there has been little research on self-reactive B cells in GD. In the current study, we reported that a unique B-cell subset, CD11c(+) B cells, was expanded in the peripheral blood (PB) of GD patients, as detected by flow cytometry. The frequency of CD11c(+) B cells was positively correlated with serum TRAb levels. The flow cytometry data showed that CD11c expression was higher in a variety of B-cell subsets and that CD11c(+) B cells presented a distinct immunophenotype compared to paired CD11c(-) B cells. Immunohistochemical and immunofluorescence staining indicated the presence of CD11c(+)CD19(+) B cells in lymphocyte infiltration areas of the GD thyroid. Flow cytometric analysis of PB and fine-needle aspiration (FNA) samples showed that compared to PB CD11c(+) B cells, CD11c(+) B cells in the thyroid accumulated and further differentiated. We found that CD11c(+) B cells from the PB of GD patients were induced to differentiate into autoreactive antibody-secreting cells (ASCs) capable of secreting TRAbs in vitro. Luminex liquid suspension chip detection data showed that CD11c(+) B cells also secreted a variety of cytokines, including proinflammatory cytokines, anti-inflammatory cytokines, and chemokines, which might play roles in regulating the local inflammatory response and infiltration of lymphocytes in the thyroid. In addition, we performed a chemotaxis assay in a Transwell chamber to verify that CD11c(+) B cells were recruited by thyroid follicular cells (TFCs) via the CXCR3-CXCL10 axis. In conclusion, our study determined that CD11c(+) B cells were involved in the pathogenesis of GD in multiple ways and might represent a promising immunotherapeutic target in the future.

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