CD11c+ T-bet+ B Cells Require IL-21 and IFN-γ from Type 1 T Follicular Helper Cells and Intrinsic Bcl-6 Expression but Develop Normally in the Absence of T-bet

J Immunol. 2020 Aug 15;205(4):1050-1058. doi: 10.4049/jimmunol.2000206. Epub 2020 Jul 17.

Abstract

CD11c+ T-bet+ B cells generated during ehrlichial infection require CD4+ T cell help and IL-21 signaling for their development, but the exact T cell subset required had not been known. In this study, we show in a mouse model of Ehrlichia muris that type 1 T follicular helper (TFH1) cells provide help to CD11c+ T-bet+ B cells via the dual secretion of IL-21 and IFN-γ in a CD40/CD40L-dependent manner. TFH1 cell help was delivered in two phases: IFN-γ signals were provided early in infection, whereas CD40/CD40L help was provided late in infection. In contrast to T-bet+ T cells, T-bet+ B cells did not develop in the absence of B cell-intrinsic Bcl-6 but were generated in the absence of T-bet. T-bet-deficient memory B cells were largely indistinguishable from their wild-type counterparts, although they no longer underwent switching to IgG2c. These data suggest that a primary function of T-bet in B cells during ehrlichial infection is to promote appropriate class switching, not lineage specification. Thus, CD11c+ memory B cells develop normally without T-bet but require Bcl-6 and specialized help from dual cytokine-producing TFH1 cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • CD11 Antigens / immunology
  • CD11 Antigens / metabolism*
  • CD40 Antigens / immunology
  • CD40 Antigens / metabolism
  • CD40 Ligand / immunology
  • CD40 Ligand / metabolism
  • Ehrlichia / immunology
  • Ehrlichia / metabolism
  • Female
  • Immunologic Memory / immunology
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism*
  • Interleukins / immunology
  • Interleukins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Proto-Oncogene Proteins c-bcl-6 / immunology
  • Proto-Oncogene Proteins c-bcl-6 / metabolism*
  • Receptors, IgG / immunology
  • Receptors, IgG / metabolism
  • T Follicular Helper Cells / immunology
  • T Follicular Helper Cells / metabolism*
  • T-Box Domain Proteins / immunology
  • T-Box Domain Proteins / metabolism*

Substances

  • Bcl6 protein, mouse
  • CD11 Antigens
  • CD40 Antigens
  • IgG2c receptor
  • Interleukins
  • Itgax protein, mouse
  • Proto-Oncogene Proteins c-bcl-6
  • Receptors, IgG
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • CD40 Ligand
  • Interferon-gamma
  • interleukin-21

Supplementary concepts

  • Ehrlichia muris