B Cell Diversification Is Uncoupled from SAP-Mediated Selection Forces in Chronic Germinal Centers within Peyer's Patches

Cell Rep. 2020 Feb 11;30(6):1910-1922.e5. doi: 10.1016/j.celrep.2020.01.032.

Abstract

Antibodies secreted within the intestinal tract provide protection from the invasion of microbes into the host tissues. Germinal center (GC) formation in lymph nodes and spleen strictly requires SLAM-associated protein (SAP)-mediated T cell functions; however, it is not known whether this mechanism plays a similar role in mucosal-associated lymphoid tissues. Here, we find that in Peyer's patches (PPs), SAP-mediated T cell help is required for promoting B cell selection in GCs, but not for clonal diversification. PPs of SAP-deficient mice host chronic GCs that are absent in T cell-deficient mice. GC B cells in SAP-deficient mice express AID and Bcl6 and generate plasma cells in proportion to the GC size. Single-cell IgA sequencing analysis reveals that these mice host few diversified clones that were subjected to mild selection forces. These findings demonstrate that T cell-derived help to B cells in PPs includes SAP-dependent and SAP-independent functions.

Keywords: B cells; IgA; Peyer’s patches; SAP; T follicular helper cells; antibody; clonal diversification; germinal center; plasma cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / immunology*
  • Germinal Center / immunology*
  • Mice
  • Peyer's Patches / immunology*
  • Signaling Lymphocytic Activation Molecule Associated Protein / metabolism*

Substances

  • Signaling Lymphocytic Activation Molecule Associated Protein