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首页> 外文期刊>Memórias do Instituto Oswaldo Cruz >Chemokines and chemokine receptors expression in the lesions of patients with American cutaneous leishmaniasis
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Chemokines and chemokine receptors expression in the lesions of patients with American cutaneous leishmaniasis

机译:美国皮肤利什曼病患者病灶中趋化因子和趋化因子受体的表达

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American cutaneous leishmaniasis (ACL) presents distinct active clinical forms with different grades of severity, known as localised (LCL), intermediate (ICL) and diffuse (DCL) cutaneous leishmaniasis. LCL and DCL are associated with a polarised T-helper (Th)1 and Th2 immune response, respectively, whereas ICL, or chronic cutaneous leishmaniasis, is associated with an exacerbated immune response and a mixed cytokine expression profile. Chemokines and chemokine receptors are involved in cellular migration and are critical in the inflammatory response. Therefore, we evaluated the expression of the chemokines CXCL10, CCL4, CCL8, CCL11 and CXCL8 and the chemokine receptors CCR3, CXCR3, CCR5 and CCR7 in the lesions of patients with different clinical forms of ACL using immunohistochemistry. LCL patients exhibited a high density of CXCL10+, CCL4+ and CCL8+ cells, indicating an important role for these chemokines in the local Th1 immune response and the migration of CXCR3+ cells. LCL patients showed a higher density of CCR7+ cells than ICL or DCL patients, suggesting major dendritic cell (DC) migration to lymph nodes. Furthermore, DCL was associated with low expression levels of Th1-associated chemokines and CCL11+ epidermal DCs, which contribute to the recruitment of CCR3+ cells. Our findings also suggest an important role for epidermal cells in the induction of skin immune responses through the production of chemokines, such as CXCL10, by keratinocytes.
机译:美国皮肤利什曼病(ACL)呈现出不同的严重程度不同的活跃临床形式,称为局部(LCL),中级(ICL)和弥散性(DCL)皮肤利什曼病。 LCL和DCL分别与极化的T辅助(Th)1和Th2免疫反应有关,而ICL或慢性皮肤利什曼病则与加剧的免疫反应和混合的细胞因子表达谱有关。趋化因子和趋化因子受体参与细胞迁移,并在炎症反应中起关键作用。因此,我们使用免疫组化方法评估了趋化因子CXCL10,CCL4,CCL8,CCL11和CXCL8以及趋化因子受体CCR3,CXCR3,CCR5和CCR7在不同临床形式ACL患者的病变中的表达。 LCL患者表现出高密度的CXCL10 +,CCL4 +和CCL8 +细胞,表明这些趋化因子在局部Th1免疫应答和CXCR3 +细胞迁移中起重要作用。 LCL患者的CCR7 +细胞密度高于ICL或DCL患者,表明主要树突状细胞(DC)迁移至淋巴结。此外,DCL与Th1相关趋化因子和CCL11 +表皮DC的低表达水平相关,这有助于CCR3 +细胞的募集。我们的发现还表明表皮细胞在通过角化细胞产生趋化因子(例如CXCL10)的诱导皮肤免疫反应中起重要作用。

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