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Article
Nature Immunology  5, 1260 - 1265 (2004)
Published online: 7 November 2004; | doi:10.1038/ni1138

Induced recruitment of NK cells to lymph nodes provides IFN-big gamma for TH1 priming

Alfonso Martín-Fontecha1, Lindy L Thomsen2, Sara Brett2, Craig Gerard3, Martin Lipp4, Antonio Lanzavecchia1 & Federica Sallusto1

1  Institute for Research in Biomedicine, 6500 Bellinzona, Switzerland.

2  Glaxo Smith and Kline, Stevenage, Herts SG12NY, UK.

3  Perlmutter Laboratory, Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.

4  Max Delbrück Center for Molecular Medicine, Berlin-Buch 13092, Germany.

Correspondence should be addressed to Alfonso Martín-Fontecha alfonso.martin-fontecha@irb.unisi.ch or Federica Sallusto federica.sallusto@irb.unisi.ch
Naive T cells are stimulated by antigen-presenting dendritic cells (DCs) in secondary lymphoid organs, but whether other types of cell participate in T cell priming is unclear. Here we show in mice that natural killer (NK) cells, which are normally excluded from lymph nodes, are rapidly recruited in a CCR7-independent, CXCR3-dependent manner to lymph nodes on stimulation by the injection of mature DCs. Recruitment of NK cells is also induced by some, but not all, adjuvants and correlates with the induction of T helper cell type 1 (TH1) responses. NK cell depletion and reconstitution experiments show that NK cells provide an early source of interferon-bold gamma (IFN-bold gamma) that is necessary for TH1 polarization. Taken together, our results identify an induced pathway of NK cell migration in antigen-stimulated lymph nodes and a mechanism by which some adjuvants may facilitate TH1 responses.

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Nature Immunology
ISSN: 1529-2908
EISSN: 1529-2916
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