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Chemokine Signatures in the Skin Disorders of Lyme Borreliosis in Europe: Predominance of CXCL9 and CXCL10 in Erythema Migrans and Acrodermatitis and CXCL13 in Lymphocytoma▿

机译:在欧洲莱姆病的皮肤疾病中趋化因子的特征:红斑偏头痛和肢端皮炎中CXCL9和CXCL10的优势以及淋巴细胞瘤中的CXCL13的优势

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摘要

The three skin disorders of Lyme borreliosis in Europe include erythema migrans, an acute, self-limited lesion; borrelial lymphocytoma, a subacute lesion; and acrodermatitis chronica atrophicans, a chronic lesion. Using quantitative reverse transcription-PCR, we determined mRNA expression of selected chemokines, cytokines, and leukocyte markers in skin samples from 100 patients with erythema migrans, borrelial lymphocytoma, or acrodermatitis chronica atrophicans and from 25 control subjects. Chemokine patterns in lesional skin in each of the three skin disorders included low but significant mRNA levels of the neutrophil chemoattractant CXCL1 and the dendritic cell chemoattractant CCL20 and intermediate levels of the macrophage chemoattractant CCL2. Erythema migrans and particularly acrodermatitis lesions had high mRNA expression of the T-cell-active chemokines CXCL9 and CXCL10 and low levels of the B-cell-active chemokine CXCL13, whereas lymphocytoma lesions had high levels of CXCL13 and lower levels of CXCL9 and CXCL10. This pattern of chemokine expression was consistent with leukocyte marker mRNA in lesional skin. Moreover, using immunohistologic methods, CD3+ T cells and CXCL9 were visualized in erythema migrans and acrodermatitis lesions, and CD20+ B cells and CXCL13 were seen in lymphocytoma lesions. Thus, erythema migrans and acrodermatitis chronica atrophicans have high levels of the T-cell-active chemokines CXCL9 and CXCL10, whereas borrelial lymphocytoma has high levels of the B-cell-active chemokine CXCL13.
机译:在欧洲,莱姆病(Lyme borreliosis)的三种皮肤疾病包括:红斑,急性,自限性病变。硼淋巴细胞瘤,一种亚急性病变;慢性萎缩性皮肤炎和慢性病变。使用定量逆转录-PCR,我们确定了来自100例红斑,红斑性淋巴瘤或慢性肩皮炎,萎缩性贫血患者的皮肤样本中以及25例对照受试者的皮肤样本中所选趋化因子,细胞因子和白细胞标志物的mRNA表达。三种皮肤病中每种病变皮肤的趋化因子模式包括中性粒细胞趋化因子CXCL1和树突状细胞趋化因子CCL20的mRNA水平低但显着,而巨噬细胞趋化因子CCL2处于中等水平。偏头痛红斑,尤其是肩皮炎病变的T细胞活性趋化因子CXCL9和CXCL10的mRNA表达较高,而B细胞活性趋化因子CXCL13的水平较低,而淋巴细胞瘤病变的CXCL13含量较高,而CXCL9和CXCL10含量较低。趋化因子的这种表达模式与病变皮肤中的白细胞标志物mRNA一致。此外,使用免疫组织学方法,在偏头痛红斑和肩周炎皮损中可见CD3 + T细胞和CXCL9,在淋巴​​细胞瘤皮损中可见CD20 + B细胞和CXCL13。因此,红斑偏头痛和慢性硬皮炎萎缩症具有高水平的T细胞活性趋化因子CXCL9和CXCL10,而硼淋巴细胞瘤具有高水平的B细胞活性趋化因子CXCL13。

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