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An immune paradox: how can the same chemokine axis regulate both immune tolerance and activation?: CCR6/CCL20: a chemokine axis balancing immunological tolerance and inflammation in autoimmune disease.

An immune paradox: how can the same chemokine axis regulate both immune tolerance and activation?: CCR6/CCL20: a chemokine axis balancing immunological tolerance and inflammation in autoimmune disease.

Authors :
Comerford I
Bunting M
Fenix K
Haylock-Jacobs S
Litchfield W
Harata-Lee Y
Turvey M
Brazzatti J
Gregor C
Nguyen P
Kara E
McColl SR
Source :
BioEssays : news and reviews in molecular, cellular and developmental biology [Bioessays] 2010 Dec; Vol. 32 (12), pp. 1067-76. Date of Electronic Publication: 2010 Oct 15.
Publication Year :
2010

Abstract

Chemokines (chemotactic cytokines) drive and direct leukocyte traffic. New evidence suggests that the unusual CCR6/CCL20 chemokine receptor/ligand axis provides key homing signals for recently identified cells of the adaptive immune system, recruiting both pro-inflammatory and suppressive T cell subsets. Thus CCR6 and CCL20 have been recently implicated in various human pathologies, particularly in autoimmune disease. These studies have revealed that targeting CCR6/CCL20 can enhance or inhibit autoimmune disease depending on the cellular basis of pathogenesis and the cell subtype most affected through different CCR6/CCL20 manipulations. Here, we discuss the significance of this chemokine receptor/ligand axis in immune and inflammatory functions, consider the potential for targeting CCR6/CCL20 in human autoimmunity and propose that the shared evolutionary origins of pro-inflammatory and regulatory T cells may contribute to the reason why both immune activation and regulation might be controlled through the same chemokine pathway.<br /> (Copyright © 2010 WILEY Periodicals, Inc.)

Details

Language :
English
ISSN :
1521-1878
Volume :
32
Issue :
12
Database :
MEDLINE
Journal :
BioEssays : news and reviews in molecular, cellular and developmental biology
Publication Type :
Academic Journal
Accession number :
20954179
Full Text :
https://doi.org/10.1002/bies.201000063