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IFNγ induces epigenetic programming of human T-bethi B cells and promotes TLR7/8 and IL-21 induced differentiation.

Esther Zumaquero | Sara L Stone | Christopher D Scharer | Scott A Jenks | Anoma Nellore | Betty Mousseau | Antonio Rosal-Vela | Davide Botta | John E Bradley | Wojciech Wojciechowski | Travis Ptacek | Maria I Danila | Jeffrey C Edberg | S Louis Bridges | Robert P Kimberly | W Winn Chatham | Trenton R Schoeb | Alexander F Rosenberg | Jeremy M Boss | Ignacio Sanz | Frances E Lund
eLife | 2019

Although B cells expressing the IFNγR or the IFNγ-inducible transcription factor T-bet promote autoimmunity in Systemic Lupus Erythematosus (SLE)-prone mouse models, the role for IFNγ signaling in human antibody responses is unknown. We show that elevated levels of IFNγ in SLE patients correlate with expansion of the T-bet expressing IgDnegCD27negCD11c+CXCR5neg (DN2) pre-antibody secreting cell (pre-ASC) subset. We demonstrate that naïve B cells form T-bethi pre-ASCs following stimulation with either Th1 cells or with IFNγ, IL-2, anti-Ig and TLR7/8 ligand and that IL-21 dependent ASC formation is significantly enhanced by IFNγ or IFNγ-producing T cells. IFNγ promotes ASC development by synergizing with IL-2 and TLR7/8 ligands to induce genome-wide epigenetic reprogramming of B cells, which results in increased chromatin accessibility surrounding IRF4 and BLIMP1 binding motifs and epigenetic remodeling of IL21R and PRDM1 loci. Finally, we show that IFNγ signals poise B cells to differentiate by increasing their responsiveness to IL-21.

Pubmed ID: 31090539

Associated grants

  • Agency: NIH HHS, United States
    Id: T32 GM008361
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI110508
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM008361
  • Agency: NIAID NIH HHS, United States
    Id: P01 AI078907
  • Agency: NIH HHS, United States
    Id: R37 AI049660
  • Agency: NCI NIH HHS, United States
    Id: P30 CA013148
  • Agency: NIH HHS, United States
    Id: UL1 TR001417
  • Agency: NIAMS NIH HHS, United States
    Id: K23 AR062100
  • Agency: NIH HHS, United States
    Id: P01 AI125180
  • Agency: Lupus Research Alliance, International
    Id: #550070
  • Agency: NIAID NIH HHS, United States
    Id: U19 AI110483
  • Agency: NIH HHS, United States
    Id: K23 AR062100
  • Agency: NIAID NIH HHS, United States
    Id: P01 AI125180
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR003096
  • Agency: NIAID NIH HHS, United States
    Id: R37 AI049660
  • Agency: NIH HHS, United States
    Id: U19 AI110483
  • Agency: NIH HHS, United States
    Id: 1P30 DK079337
  • Agency: NIH Office of the Director, International
    Id: 1P30 DK079337
  • Agency: NIH HHS, United States
    Id: P01 AI078907
  • Agency: NIH HHS, United States
    Id: R01 AI110508
  • Agency: NIH HHS, United States
    Id: R01 AI123733
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI123733
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR001417

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