Follicular Regulatory T Cells Can Access the Germinal Center Independently of CXCR5

Cell Rep. 2020 Jan 21;30(3):611-619.e4. doi: 10.1016/j.celrep.2019.12.076.

Abstract

The germinal center (GC) response is critical for generating high-affinity humoral immunity and immunological memory, which forms the basis of successful immunization. Control of the GC response is thought to require follicular regulatory T (Tfr) cells, a subset of suppressive Foxp3+ regulatory T cells located within GCs. Relatively little is known about the exact role of Tfr cells within the GC and how they exert their suppressive function. A unique feature of Tfr cells is their reported CXCR5-dependent localization to the GC. Here, we show that the lack of CXCR5 on Foxp3+ regulatory T cells results in a reduced frequency, but not an absence, of GC-localized Tfr cells. This reduction in Tfr cells is not sufficient to alter the magnitude or output of the GC response. This demonstrates that additional, CXCR5-independent mechanisms facilitate Treg cell homing to the GC.

Keywords: CXCR5; follicular regulatory T cells; germinal center response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Forkhead Transcription Factors / metabolism
  • Gene Deletion
  • Germinal Center / immunology*
  • Lymphocyte Count
  • Mice, Inbred C57BL
  • Orthomyxoviridae Infections / immunology
  • Receptors, CXCR5 / metabolism*
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Receptors, CXCR5