D'Ambrosio D, Iellem A, Bonecchi R, Mazzeo D, Sozzani S, Mantovani A, Sinigaglia F
Roche Milano Ricerche, Milan, Italy.
J Immunol. 1998 Nov 15;161(10):5111-5.
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.
极化的Th1细胞和Th2细胞差异表达黏附分子和趋化因子受体,使这些细胞具有不同的组织归巢能力。我们在此报告,与其他趋化因子受体不同,TCR和CD28激活后,Th2细胞上CCR4和CCR8的表达会短暂增加。这种激活诱导的CCR4和CCR8上调不需要IL-4。与受体表达一致,激活后Th2细胞对I-309(CCR8配体)和胸腺激活调节趋化因子(CCR4和CCR8配体)的反应增强。此外,活化的Th1细胞上调CCR4表达以及对胸腺激活调节趋化因子的功能反应性。对CD8+T细胞极化亚群的分析揭示了趋化因子受体表达和反应性调节的类似模式。综上所述,这些发现表明抗原接触后CCR4和CCR8的上调可能有助于活化T细胞在抗原攻击部位和/或淋巴组织特定区域内的正确定位。