Human Th17 cells share major trafficking receptors with both polarized effector T cells and FOXP3(+) regulatory T cells

Hyung W. Lim, Purdue University - Main Campus
Jeeho Lee, Purdue University - Main Campus
Peter Hillsamer, Sagamore Surg Ctr, Lafayette, IN 47909
Chang H. Kim, Purdue University - Main Campus

Date of this Version

1-2008

Citation

JOURNAL OF IMMUNOLOGY Volume: 180 Issue: 1 Pages: 122-129

This document has been peer-reviewed.

 

Abstract

It is a question of interest whether Th17 cells express trafficking receptors unique to this Th cell lineage and migrate specifically to certain tissue sites. We found several Th17 cell subsets at different developing stages in a human secondary lymphoid organ (tonsils) and adult, but not in neonatal, blood. These Th17 cell subsets include a novel in vivo-stimulated tonsil IL17(+) T cell subset detected without any artificial stimulation in vitro. We investigated in depth the trafficking receptor phenotype of the Th17 cell subsets in tonsils and adult blood. The developing Th17 cells in tonsils highly expressed both Th1- (CCR2, CXCR3, CCR5, and CXCR6) and Th2-associated (CCR4) trafficking receptors. Moreover, Th17 cells share major non-lymphoid tissue trafficking receptors, such as CCR4, CCR5, CCR6, CXCR3, and CXCR6, with FOXP3(+) T regulatory cells. In addition, many Th17 cells express homeostatic chemokine receptors (CD62L, CCR6, CCR7, CXCR4, and CXCR5) implicated in T cell migration to and within lymphoid tissues. Expression of CCR6 and CCR4 by some Th17 cells is not a feature unique to Th17 cells but shared with FOXP3(+) T cells. Interestingly, the IL17(+)IFN-gamma(+) Th17 cells have the features of both IL17(-)IFN-gamma(+) Th1 and IL17(+)IFN-gamma(-) Th17 cells in expression of trafficking receptors. Taken together, our results revealed that Th17 cells are highly heterogeneous, in terms of trafficking receptors, and programmed to share major trafficking receptors with other T cell lineages. These findings have important implications in their distribution in the human body in relation to other regulatory T cell subsets.

 

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