伊拉克皮肤利什曼病的MIF G-173C多态性及易感性

G. B. Alomashi, Hasan Khudhur
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引用次数: 1

摘要

人类利什曼病是一种由沙蝇传播的寄生虫病,其特点是一系列皮肤、粘膜和内脏疾病,主要取决于所涉寄生虫的种类和宿主的免疫反应。1,2皮肤利什曼病是利什曼病最常见的形式,每年约有(100 - 150万)例,约占全世界所有病例的(50 - 70%)。2,3皮肤利什曼病每年发生,90%以上的病例发生在旧世界的五个国家(阿富汗、阿尔及利亚、伊朗、伊拉克和沙特阿拉伯)和新世界的两个国家,包括巴西和秘鲁。4在伊拉克,主要利什曼原虫和热带利什曼原虫被认为是皮肤利什曼病的常见病因。5巨噬细胞迁移抑制因子(MIF)被认为是最早发现的细胞因子之一。它被认为是宿主对微生物免疫反应的重要组成部分,并诱导免疫细胞激活和分泌白细胞介素,如TNF-α、IFN-γ、IL -1β、IL-12、IL-6和IL-8MIF通过抑制P53活性提高巨噬细胞存活率,从而减少活化诱导的细胞凋亡。7,8最后,1989年在人体内克隆了cDNA, MIF基因组定位于22q11染色体,人类MIF基因有3个外显子,分别为205、173和183 bp,由两个内含子分隔,分别为189和95 bp。6,9既往研究表明,MIF在宿主对皮肤利什曼病的抵抗中起着至关重要的作用,发现人MIF在体外以1.5 -2.5μg/ ml的浓度激活被感染的巨噬细胞杀死L. majorJesus等在巴西发现MIF-173 C多态性与皮肤利什曼病相关Jesus提示,MIF- 173c等位基因诱导血清中MIF细胞因子水平降低,而这种低水平的MIF合成可能与利什曼病易感性相关。本研究旨在探讨AL-Muthanna省伊拉克人群中mif - 173c多态性与CL感染易感性的关系。材料与方法
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MIF G-173C polymorphism and susceptibility to cutaneous leishmaniasis in Iraq
Human leishmaniasis is a parasitic disease transmitted by sand flies, its characteristic by a spectrum of cutaneous, mucocutaneous and visceral diseases that depend largely on the species of the parasite involved and host immune response.1,2 Cutaneous leishmaniasis is the most common form of leishmaniasis, about (1-1.5) million of cases every year, and about (50 to 70%) of all cases in the world.2,3 Cutaneous leishmaniasis occurs each year more than 90% of cases occur in five countries in the old word (Afghanistan, Algeria, Iran, Iraq and Saudi Arabia) and two countries in the new world including Brazil and Peru.4 Leishmania major and Leishmania tropica considered as common causes of Cutaneous leishmaniasis in Iraq.5 Macrophage migration inhibitory factor (MIF) is considered to be one of the first cytokines to be discovered, its consider an essential component of the immune response of host against microbial and induce activation and secretion of interleukins like TNF-α, IFN-γ, IL -1β, IL-12, IL-6 and IL-8 by immune cells.6 MIF increase survival of macrophage by inhibition activity of P53 and thus decrease activation-induced apoptosis.7,8 Finally, cDNA was cloned in 1989 in human, MIF genomic localization to chromosome 22q11 later mapped, the human MIF gene has three exons of 205, 173 and 183 bp, these are separated by two introns of 189 and 95 bp.6,9 Previous study refer to that MIF plays an essential role in resistance of host to Cutaneous leishmaniasis, were found human MIF activate infected macrophage to kill L. major at a concentration (1.5 -2.5μg/ ml) in vitro.10 Jesus et al in Brazil found that associated between MIF-173 C polymorphism and cutaneous leishmaniasis.11 Jesus suggest that the MIF-173C allele induce lower levels of MIF cytokine in serum, and this lower synthesis of MIF might behave correlation with susceptibility to leishmaniasis. The present study aims to investigate of MIF-173 C polymorphism with susceptibility to CL infection in Iraqi population in AL-Muthanna province. Material and methods
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