[Immuno-modulating effects of eukaryotic expressing vectors of IL-12 and GM-CSF associated to DNA-based vaccination against experimental cutaneous leishmaniasis in BALB/c mouse].

S Ben Hadj Ahmed, K Dellagi, C Bahloul
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Abstract

Different works of DNA based vaccination against leishmaniasis highlight the complexity of the induced immune responses to fight against the disease. In this work, we exploited the capacity of IL-12 and GMC-SF to activate immune cell mediators and effectors to induce a Th1 response, more capable of clearing the parasite. To generate these immunomodulating activities, we associated eukaryotic expressing vectors of murine IL-12 and GMC-SF to several DNA based vaccine candidates encoding to several L. (L.) major antigens, in the BALB/c mouse. When mice were challenged with a high parasitic load in the hind footpad, no additional protective effect could be generated. However, when the challenge was carried out in the inner face of the ear with a small parasitic load, the association of plasmids encoding to IL-12 and GMC-SF to DNA based vaccination, the protective effects were increased.

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[IL-12和GM-CSF真核表达载体对BALB/c小鼠实验性皮肤利什曼病的免疫调节作用]。
针对利什曼病的DNA疫苗接种的不同工作突出了对抗该疾病的诱导免疫反应的复杂性。在这项工作中,我们利用IL-12和GMC-SF的能力激活免疫细胞介质和效应物,诱导Th1反应,更有能力清除寄生虫。为了产生这些免疫调节活性,我们在BALB/c小鼠中将小鼠IL-12和GMC-SF的真核表达载体与编码多种L. (L.)主要抗原的几种基于DNA的候选疫苗联系起来。当小鼠后足部寄生负荷较高时,不产生额外的保护作用。然而,当在小寄生负荷的情况下在耳内面进行攻击时,编码IL-12和GMC-SF的质粒与基于DNA的疫苗接种的关联,保护作用增强。
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