Journal article

CXCR3 Chemokine Receptor-Ligand Interactions in the Lymph Node Optimize CD4 T Helper 1 Cell Differentiation

JR Groom, J Richmond, TT Murooka, EW Sorensen, JH Sung, K Bankert, UH von Andrian, JJ Moon, TR Mempel, AD Luster

Immunity | CELL PRESS | Published : 2012

Abstract

Differentiation of naive CD4+ T cells into T helper (Th) cells is a defining event in adaptive immunity. The cytokines and transcription factors that control Th cell differentiation are understood, but it is not known how this process is orchestrated within lymph nodes (LNs). Here we have shown that the CXCR3 chemokine receptor was required for optimal generation of interferon-γ (IFN-γ)-secreting Th1 cells in vivo. By using a CXCR3 ligand reporter mouse, we found that stromal cells predominately expressed the chemokine ligand CXCL9 whereas hematopoietic cells expressed CXCL10 in LNs. Dendritic cell (DC)-derived CXCL10 facilitated T cell-DC interactions in LNs during T cell priming while both..

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University of Melbourne Researchers

Grants

Awarded by National Institute of Allergy and Infectious Diseases


Funding Acknowledgements

Work was supported by the NIH grants CA069212 (to A.D.L.) and A1078897 (to U.H.v.A.). J.R.G. was supported by the NH&MRC, Australia (Fellowship 516791). J.H.S. was supported by a Samsung Scholarship. We thank D. Alvarez for assistance with LCMV infections, J. Farber for the Cxcl9<SUP>-/-</SUP> breeding breeding pair, and C. Gerard for the Cxcr3<SUP>-/-</SUP> breeding pair.