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弥漫性皮肤利什曼病中与治疗反应相关的细胞因子模式变化

Variation of cytokine patterns related to therapeutic response in diffuse cutaneous leishmaniasis.

作者信息

Bomfim G, Nascimento C, Costa J, Carvalho E M, Barral-Netto M, Barral A

机构信息

Serviço de Imunologia (HUPES-FAMED), Universidade Federal da Bahia, Brazil.

出版信息

Exp Parasitol. 1996 Nov;84(2):188-94. doi: 10.1006/expr.1996.0104.

DOI:10.1006/expr.1996.0104
PMID:8932768
Abstract

Diffuse cutaneous leishmaniasis is a rare entity characterized by disseminated cutaneous nodules associated with specific anergy to leishmanial antigens. A low but not absent IFN-gamma expression by cells present in cutaneous lesions has been documented during the active phase of diffuse cutaneous leishmaniasis. In this study we confirm this observation, and extend it by showing a similar pattern in peripheral blood mononuclear cells and the variation of mRNA cytokine expression pattern during different stages of the disease. During active disease, patients did not express mRNA for IFN-gamma, while expressing mRNA for IL-2, IL-4, and IL-10. In contrast, an expression of IFN-gamma and low IL-10 was observed after treatment-induced transient healing of cutaneous lesions. In three patients we have been able to analyze a third PBMC sample obtained after clinical relapse, documenting in all of them decreased IFN-gamma expression with no expression of IL-10. Although there was an association between the appearance of IFN-gamma expression and clinical improvement, with marked expression of IFN-gamma mRNA and decreased expression of mRNA for IL-10 after treatment, this was not sufficient to prevent relapse in these patients. Therefore, it is possible that factors other than the cytokines characteristic of the Th1 and Th2 balance are implicated in the inability of diffuse cutaneous leishmaniasis patients to mount an anti-Leishmania immune response causing clinical improvement.

摘要

弥漫性皮肤利什曼病是一种罕见的疾病,其特征为散在性皮肤结节,并伴有对利什曼原虫抗原的特异性无反应性。在弥漫性皮肤利什曼病的活动期,已记录到皮肤病变部位存在的细胞有低水平但并非完全没有的γ干扰素表达。在本研究中,我们证实了这一观察结果,并通过显示外周血单核细胞中类似的模式以及疾病不同阶段mRNA细胞因子表达模式的变化对其进行了扩展。在疾病活动期,患者不表达γ干扰素的mRNA,而表达白细胞介素-2、白细胞介素-4和白细胞介素-10的mRNA。相反,在治疗诱导皮肤病变短暂愈合后,观察到γ干扰素表达以及低水平的白细胞介素-10。在三名患者中,我们能够分析临床复发后获得的第三份外周血单核细胞样本,所有样本均显示γ干扰素表达降低且白细胞介素-10无表达。尽管γ干扰素表达的出现与临床改善之间存在关联,治疗后γ干扰素mRNA有明显表达且白细胞介素-10的mRNA表达降低,但这并不足以防止这些患者复发。因此,除了Th1和Th2平衡特征性的细胞因子之外,可能还有其他因素导致弥漫性皮肤利什曼病患者无法产生导致临床改善的抗利什曼原虫免疫反应。

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