Regulation of T(H)2 development by CXCR5+ dendritic cells and lymphotoxin-expressing B cells

Nat Immunol. 2012 May 27;13(7):681-90. doi: 10.1038/ni.2309.

Abstract

Although cognate encounters between antigen-bearing dendritic cells (DCs) that express the chemokine receptor CCR7 and CCR7(+) naive T cells take place in the T cell zone of lymph nodes, it is unknown whether the colocalization of DCs and T cells in the T cell area is required for the generation of effector cells. Here we found that after infection with an intestinal nematode, antigen-bearing DCs and CD4(+) T cells upregulated the chemokine receptor CXCR5 and localized together outside the T cell zone by a mechanism dependent on the chemokine CXCL13, B cells and lymphotoxin. Notably, lymphotoxin-expressing B cells, CXCR5-expressing DCs and T cells, and CXCL13 were also necessary for development of interleukin 4 (IL-4)-producing type 2 helper T cells (T(H)2 cells), which suggests that T(H)2 differentiation can initiate outside the T cell zone.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / immunology*
  • Chemokine CXCL13 / immunology
  • Dendritic Cells / immunology*
  • Interleukin-4 / immunology
  • Lymphocyte Activation / immunology
  • Lymphotoxin-alpha / biosynthesis
  • Lymphotoxin-alpha / genetics
  • Lymphotoxin-alpha / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Nematospiroides dubius / immunology
  • Receptors, CXCR5 / immunology*
  • Strongylida Infections / immunology*
  • Th2 Cells / immunology*

Substances

  • CXCR5 protein, mouse
  • Chemokine CXCL13
  • Cxcl13 protein, mouse
  • Lymphotoxin-alpha
  • Receptors, CXCR5
  • Interleukin-4