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巴西印第安人局限性皮肤利什曼病皮损细胞因子和趋化因子的基因表达谱。

Gene expression profile of cytokines and chemokines in skin lesions from Brazilian Indians with localized cutaneous leishmaniasis.

机构信息

Laboratório de Biomarcadores de Diagnóstico e Monitoração, Centro de Pesquisas René Rachou, Fundação Oswaldo Cruz, FIOCRUZ, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Mol Immunol. 2014 Feb;57(2):74-85. doi: 10.1016/j.molimm.2013.08.008. Epub 2013 Sep 28.

Abstract

Cutaneous leishmaniasis (CL) is a chronic inflammatory disease caused by dermotropic Leishmania species belonging to the Viannia subgenera, with Leishmania (V.) braziliensis considered the main agent in Brazil. After infection, a local inflammatory process is initiated, inducing the expression of several cytokine/chemokine genes. We evaluated the immunity to CL of patients living in the indigenous community Xakriabá, Minas Gerais state, Brazil, by performing detailed analyses of the mRNA expression of different cytokines and chemokines in CL lesions, considering the time evolution (recent or late). We also studied the profile of the inflammatory infiltrate by histopathological analysis. The histopathological features of recent CL lesions showed an intense inflammatory reaction, characterized by the presence of both mononuclear and polymorphonuclear cells, whereas late CL lesions exhibited a predominance of mononuclear leukocytes. The gene expression of cytokines/chemokines in skin biopsies from the CL group showed higher transcript levels of modulatory (IL10 and TGFB1), anti-inflammatory (IL4), and pro-inflammatory (TNF, IFNG, IL12B, CCL2, CCL3, CCL5, CXCL10) biomarkers in recent lesions than in late lesions. Our findings suggest that differential gene expression of cytokines and chemokines found in skin lesions from CL patients is associated with time evolution of lesions.

摘要

皮肤利什曼病(CL)是一种由亲表皮利什曼原虫属的种属引起的慢性炎症性疾病,其中 Leishmania (V.) braziliensis 被认为是巴西的主要病原体。感染后,会引发局部炎症过程,诱导多种细胞因子/趋化因子基因的表达。我们通过对巴西米纳斯吉拉斯州 Xakriabá 原住民社区的 CL 患者进行详细的细胞因子/趋化因子 mRNA 表达分析,评估了他们对 CL 的免疫反应,同时考虑了时间演变(近期或晚期)。我们还通过组织病理学分析研究了炎症浸润的特征。近期 CL 病变的组织病理学特征显示出强烈的炎症反应,其特征是单核细胞和多形核细胞均存在,而晚期 CL 病变则以单核白细胞为主。CL 组皮肤活检的细胞因子/趋化因子基因表达显示,近期病变的调节因子(IL10 和 TGFB1)、抗炎因子(IL4)和促炎因子(TNF、IFNG、IL12B、CCL2、CCL3、CCL5、CXCL10)的转录水平高于晚期病变。我们的研究结果表明,CL 患者皮肤病变中细胞因子和趋化因子的差异表达与病变的时间演变有关。

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