[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]。

S Ben Hadj Ahmed, K Dellagi, C Bahloul
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引用次数: 0

摘要

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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[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].

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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