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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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 681-90MeSH
AnimalsB-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 ArticleResearch Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
22634865
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