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首页> 外文期刊>Acta tropica: Journal of Biomedical Sciences >Studies on the protective efficacy and immunogenicity of Hsp70 and Hsp83 based vaccine formulations in Leishmania donovani infected BALB/c mice.
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Studies on the protective efficacy and immunogenicity of Hsp70 and Hsp83 based vaccine formulations in Leishmania donovani infected BALB/c mice.

机译:基于Hsp70和Hsp83的疫苗制剂在利什曼原虫感染BALB / c小鼠中的保护功效和免疫原性的研究。

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摘要

Visceral leishmaniasis, a chronic systemic infection, is the major cause of morbidity and mortality in many parts of world. The current drugs for the treatment of leishmaniasis are toxic, expensive, difficult to administer and becoming ineffective due to the emergence of drug resistance. In the absence of effective treatment, vaccination remains the only hope for control of the disease. We have evaluated the protective efficacy of two heat shock proteins (Hsp70 and Hsp83) in combination with two different adjuvants (MPLA and ALD) in Leishmania donovani infected inbred BALB/c mice. The proteins were isolated by SDS-PAGE and the mice were immunized subcutaneously with Hsp70+Hsp83, Hsp70+Hsp83+ALD and Hsp70+Hsp83+MPLA. These were challenged with 10(7) promastigotes of L. donovani. The animals were sacrificed on 30, 60 and 90 days post challenge for the assessment of parasite load and generation of cellular and humoral immune responses. The vaccines induced a strong protective response against experimental visceral leishmaniasis as shown by reduced parasite load in liver of all immunized groups as compared to the infected controls. The vaccines also led to the augmentation of DTH responses, increased levels of IgG2a, IFN-gamma and IL-2. Both the adjuvants raised significantly the level of protection imparted by the proteins but MPLA was more effective in comparison to ALD.
机译:内脏利什曼病是一种慢性全身性感染,是世界许多地方发病和死亡的主要原因。当前用于治疗利什曼病的药物是有毒的,昂贵的,难以施用的并且由于耐药性的出现而变得无效。在缺乏有效治疗的情况下,接种疫苗仍然是控制该病的唯一希望。我们已经评估了两种热休克蛋白(Hsp70和Hsp83)与两种不同的佐剂(MPLA和ALD)的组合在利什曼原虫感染的近交B​​ALB / c小鼠中的保护作用。通过SDS-PAGE分离蛋白质,并用Hsp70 + Hsp83,Hsp70 + Hsp83 + ALD和Hsp70 + Hsp83 + MPLA皮下免疫小鼠。这些受到了多诺尼乳杆菌的10(7)前鞭毛体的攻击。攻击后30、60和90天处死动物,以评估寄生虫负荷以及细胞和体液免疫应答的产生。该疫苗诱导了针对实验性内脏利什曼病的强烈保护性反应,如与受感染的对照组相比,所有免疫组的肝脏中的寄生虫载量减少都表明了这种疫苗。疫苗还导致DTH反应增强,IgG2a,IFN-γ和IL-2水平升高。两种佐剂均显着提高了蛋白质赋予的保护水平,但与ALD相比,MPLA更有效。

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