Disordered T cell-B cell interactions in autoantibody-positive inflammatory arthritis

Citation:

Amélie M Julé, Ki Pui Lam, Maria Taylor, Kacie J Hoyt, Kevin Wei, Maria Gutierrez-Arcelus, Siobhan M Case, Mia Chandler, Margaret H Chang, Ezra M Cohen, Fatma Dedeoglu, Olha Halyabar, Jonathan Hausmann, Melissa M Hazen, Erin Janssen, Jeffrey Lo, Mindy S Lo, Esra Meidan, Jordan E Roberts, Holly Wobma, Mary Beth F Son, Robert P Sundel, Pui Y Lee, Peter T Sage, Talal A Chatila, Peter A Nigrovic, Deepak A Rao, and Lauren A Henderson. 1/5/2023. “Disordered T cell-B cell interactions in autoantibody-positive inflammatory arthritis.” Front Immunol, 13, Pp. 1068399.

Abstract:

T peripheral helper (Tph) cells, identified in the synovium of adults with seropositive rheumatoid arthritis, drive B cell maturation and antibody production in non-lymphoid tissues. We sought to determine if similarly dysregulated T cell-B cell interactions underlie another form of inflammatory arthritis, juvenile oligoarthritis (oligo JIA). Clonally expanded Tph cells able to promote B cell antibody production preferentially accumulated in the synovial fluid (SF) of oligo JIA patients with antinuclear antibodies (ANA) compared to autoantibody-negative patients. Single-cell transcriptomics enabled further definition of the Tph gene signature in inflamed tissues and showed that Tph cells from ANA-positive patients upregulated genes associated with B cell help to a greater extent than patients without autoantibodies. T cells that co-expressed regulatory T and B cell-help factors were identified. The phenotype of these Tph-like Treg cells suggests an ability to restrain T cell-B cell interactions in tissues. Our findings support the central role of disordered T cell-help to B cells in autoantibody-positive arthritides.
Last updated on 06/08/2023