B cell ADAM17 controls T cell independent humoral immune responses through regulation of TACI and CD138

Biochem Biophys Res Commun. 2020 Feb 5;522(2):442-447. doi: 10.1016/j.bbrc.2019.11.124. Epub 2019 Nov 23.

Abstract

ADAM17 is known to contribute to the immune system through its shedding of tumor necrosis factor alpha (TNFα). However, the role of ADAM17 in B cell biology is not well characterized. To determine whether B cell ADAM17 contributes to T cell-independent humoral immune responses, we crossed CD19 Cre transgenic mice with mice bearing a floxed allele of ADAM17 (ADAM17CD19). In this study, we show a B cell intrinsic role for ADAM17 in regulating marginal zone B cell (MZB) numbers in mice. Interestingly, we demonstrate that the loss of B cell ADAM17 results in reduced MZB numbers in the naïve state and after immunization with T-independent antigen, yet enhanced humoral immunity to T cell independent antigens. We additionally find elevated TACI and CD138 levels on plasma cells following immunization in ADAM17CD19 mice. Overall, these findings suggest that B cell ADAM17 may orchestrate T independent immune responses through both MZB numbers and plasma cell antibody production.

Keywords: ADAM17; Humoral immunity; Marginal zone B cell; Plasma cell; T cell independent.

Publication types

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

MeSH terms

  • ADAM17 Protein / metabolism*
  • Animals
  • B-Lymphocytes / immunology*
  • Biomarkers / metabolism
  • Cell Survival
  • Immunity, Humoral*
  • Immunization
  • Mice, Transgenic
  • Plasma Cells / metabolism
  • Syndecan-1 / metabolism*
  • T-Lymphocytes / immunology*
  • Transmembrane Activator and CAML Interactor Protein / metabolism*

Substances

  • Biomarkers
  • Syndecan-1
  • Tnfrsf13b protein, mouse
  • Transmembrane Activator and CAML Interactor Protein
  • ADAM17 Protein