Distinct T helper cell dependence of memory B-cell proliferation versus plasma cell differentiation

Immunology. 2017 Mar;150(3):329-342. doi: 10.1111/imm.12688. Epub 2017 Jan 5.

Abstract

Several memory B-cell subclasses with distinct functions have been described, of which the most effective is the class-switched (CS) memory B-cell population. We have previously shown, using virus-like particles (VLPs), that the proliferative potential of these CS memory B cells is limited and they fail to re-enter germinal centres (GCs). However, VLP-specific memory B cells quickly differentiated into secondary plasma cells (PCs) with the virtue of elevated antibody production compared with primary PCs. Whereas the induction of VLP+ memory B cells was strongly dependent on T helper cells, we were wondering whether re-stimulation of VLP+ memory B cells and their differentiation into secondary PCs would also require T helper cells. Global absence of T helper cells led to strongly impaired memory B cell proliferation and PC differentiation. In contrast, lack of interleukin-21 receptor-dependent follicular T helper cells or CD40 ligand signalling strongly affected proliferation of memory B cells, but differentiation into mature secondary PCs exhibiting increased antibody production was essentially normal. This contrasts with primary B-cell responses, where a strong dependence on CD40 ligand but limited importance of interleukin-21 receptor was seen. Hence, T helper cell dependence differs between primary and secondary B-cell responses as well as between memory B-cell proliferation and PC differentiation.

Keywords: T helper cell-dependent immune response; antibodies; memory B cells; plasma cell differentiation; secondary response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibody Formation
  • B-Lymphocyte Subsets / immunology*
  • B-Lymphocytes / immunology*
  • CD40 Ligand / genetics
  • Cell Differentiation
  • Cell Proliferation
  • Cytokines / metabolism
  • Immunologic Memory* / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Plasma Cells / immunology*
  • Receptors, Interleukin-21 / genetics
  • T-Lymphocytes, Helper-Inducer / immunology*

Substances

  • Cytokines
  • Receptors, Interleukin-21
  • CD40 Ligand