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Disordered T cell-B cell interactions in autoantibody-positive inflammatory arthritis.
Julé, Amélie M; Lam, Ki Pui; Taylor, Maria; Hoyt, Kacie J; Wei, Kevin; Gutierrez-Arcelus, Maria; Case, Siobhan M; Chandler, Mia; Chang, Margaret H; Cohen, Ezra M; Dedeoglu, Fatma; Halyabar, Olha; Hausmann, Jonathan; Hazen, Melissa M; Janssen, Erin; Lo, Jeffrey; Lo, Mindy S; Meidan, Esra; Roberts, Jordan E; Wobma, Holly; Son, Mary Beth F; Sundel, Robert P; Lee, Pui Y; Sage, Peter T; Chatila, Talal A; Nigrovic, Peter A; Rao, Deepak A; Henderson, Lauren A.
Afiliação
  • Julé AM; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Lam KP; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Taylor M; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Hoyt KJ; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Wei K; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Gutierrez-Arcelus M; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Case SM; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Chandler M; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA, United States.
  • Chang MH; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Cohen EM; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Dedeoglu F; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Halyabar O; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Hausmann J; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Hazen MM; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Janssen E; Division of Rheumatology, Boston Medical Center, Boston University School of Medicine, Boston, MA, United States.
  • Lo J; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Lo MS; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Meidan E; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Roberts JE; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Wobma H; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Son MBF; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Sundel RP; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Lee PY; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Sage PT; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Chatila TA; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Nigrovic PA; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Rao DA; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Henderson LA; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
Front Immunol ; 13: 1068399, 2022.
Article em En | MEDLINE | ID: mdl-36685593
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Artrite Reumatoide Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Juvenil / Artrite Reumatoide Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Front Immunol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos