Cutting edge: selective up-regulation of chemokine receptors CCR4 and CCR8 upon activation of polarized human type 2 Th cells

D D'Ambrosio, A Iellem, R Bonecchi… - The Journal of …, 1998 - journals.aai.org
D D'Ambrosio, A Iellem, R Bonecchi, D Mazzeo, S Sozzani, A Mantovani, F Sinigaglia
The Journal of Immunology, 1998journals.aai.org
Abstract Polarized Th1 and Th2 cells differentially express adhesion molecules and
chemokine receptors, endowing these cells with distinct tissue homing capabilities. Here we
report that, in contrast to other chemokine receptors, the expression of CCR4 and CCR8 on
Th2 cells is transiently increased following TCR and CD28 engagement. IL-4 is not required
for this activation-induced up-regulation of CCR4 and CCR8. In accordance with receptor
expression, the response of Th2 cells to I-309 (CCR8 ligand) and thymus-and activation …
Abstract
Polarized Th1 and Th2 cells differentially express adhesion molecules and chemokine receptors, endowing these cells with distinct tissue homing capabilities. Here we report that, in contrast to other chemokine receptors, the expression of CCR4 and CCR8 on Th2 cells is transiently increased following TCR and CD28 engagement. IL-4 is not required for this activation-induced up-regulation of CCR4 and CCR8. In accordance with receptor expression, the response of Th2 cells to I-309 (CCR8 ligand) and thymus-and activation-regulated chemokine (CCR4 and CCR8 ligand) is enhanced upon activation. Moreover, activated Th1 cells up-regulate CCR4 expression and functional responsiveness to thymus-and activation-regulated chemokine. Analysis of polarized subsets of CD8+ T cells reveals a similar pattern of chemokine receptor expression and modulation of responsiveness. Taken together, these findings suggest that an up-regulation of CCR4 and CCR8 following Ag encounter may contribute to the proper positioning of activated T cells within sites of antigenic challenge and/or specialized areas of lymphoid tissues.
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