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胸腺与激活调节趋化因子(TARC/CCL17)在小鼠皮内注射时可诱导以Th2为主导的炎症反应。

Thymus- and activation-regulated chemokine (TARC/CCL17) induces a Th2-dominated inflammatory reaction on intradermal injection in mice.

作者信息

Vestergaard Christian, Deleuran Mette, Gesser Borbala, Larsen Christian Grønhøj

机构信息

Department of Dermatology, Marselisborg Research Center, Research Laboratory D, Aarhus, Denmark.

出版信息

Exp Dermatol. 2004 Apr;13(4):265-71. doi: 10.1111/j.0906-6705.2004.00149.x.

DOI:10.1111/j.0906-6705.2004.00149.x
PMID:15086343
Abstract

TARC/CCL17 (thymus- and activation-regulated chemokine) is a CC chemokine, which binds to the CC chemokine receptor-4 (CCR4) known to be distinctively expressed on Th2 lymphocytes. In atopic dermatitis (AD), the skin is invaded by Th2 lymphocytes in the acute phase. TARC/CCL17 is produced by the keratinocytes in AD lesions, and CCR4 is overexpressed on CLA+ (cutaneous lymphocyte-associated antigen) lymphocytes in the skin and blood. We, therefore, hypothesized that TARC/CCL17 is pivotal in mediating a Th2-dominated inflammation in the skin. To examine this, we injected BALB/c mice with murine TARC/CCL17 in concentrations ranging from 0.1 microg/ml to 10 microg/ml and examined the skin after 48 h. This revealed that TARC/CCL17 induces lymphocytic infiltration of the skin by CD4+ lymphocytes in a dose-dependent manner with a maximum response at 1 microg/ml. Additionally, TARC/CCL17 induced interleukin-4 mRNA but not interferon-gamma mRNA expression in the skin, suggesting that the lymphocytes invading the skin are Th2 cells. Additionally, TARC/CCL17 induced its own production in the keratinocytes along with cutaneous T-cell-attracting chemokine (CTACK/CCL27) mRNA. We, therefore, conclude that TARC/CCL17 induces a Th2-dominated inflammatory reaction when injected into the skin.

摘要

胸腺和活化调节趋化因子(TARC/CCL17)是一种CC趋化因子,它与已知在Th2淋巴细胞上特异性表达的CC趋化因子受体4(CCR4)结合。在特应性皮炎(AD)中,急性期皮肤会受到Th2淋巴细胞的侵袭。TARC/CCL17由AD皮损中的角质形成细胞产生,CCR4在皮肤和血液中的CLA +(皮肤淋巴细胞相关抗原)淋巴细胞上过度表达。因此,我们推测TARC/CCL17在介导皮肤中以Th2为主导的炎症中起关键作用。为了验证这一点,我们给BALB/c小鼠注射浓度范围为0.1μg/ml至10μg/ml的鼠源TARC/CCL17,并在48小时后检查皮肤。结果显示,TARC/CCL17以剂量依赖的方式诱导CD4 +淋巴细胞对皮肤的淋巴细胞浸润,在1μg/ml时反应最大。此外,TARC/CCL17在皮肤中诱导白细胞介素-4 mRNA表达,但不诱导干扰素-γ mRNA表达,这表明侵入皮肤的淋巴细胞是Th2细胞。此外,TARC/CCL17在角质形成细胞中诱导自身产生以及皮肤T细胞吸引趋化因子(CTACK/CCL27)mRNA。因此,我们得出结论,当注入皮肤时,TARC/CCL17会诱导以Th2为主导的炎症反应。

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