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

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.

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  • Publisher Full Text
  • Authors

    León B, Ballesteros-Tato A, Browning JL, Dunn R, Randall TD, Lund FE

    Institution

    Department of Medicine, Division of Allergy, Immunology and Rheumatology, University of Rochester Medical Center, Rochester, New York, USA.

    Source

    Nature immunology 13:7 2012 Jul pg 681-90

    MeSH

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

    Pub Type(s)

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

    Language

    eng

    PubMed ID

    22634865