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A New Vaccine Strategy of Dendritic Cell Presented Kinetoplastid Membrane (KMP-11) as Immunogen for Control against Experimental Visceral Leishmaniasis

机译:树突细胞的新疫苗策略呈现Kinetoplastid膜(KMP-11)作为免疫原,用于防止实验内脏LeishManiaisis

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Available reports suggest that, Leishmania donovani antigen KMP-11 may be significant in the modulation of immune responses in visceral leishmaniasis (VL). This study evaluated vaccine prospect of presentation of KMP-11 antigen through murine dendritic cells against VL in infected BALB/c mice. We report here that immunization with KMP-11 delivered through bone marrow derived dendritic cells can lead to killing of L. donovani in infected BALB/c mice. Furthermore, the strategy to use KMP-11 as vaccine delivered through DCs can stimulate the production of IFN-g, IL-12, IL-2R and TNF-α with concomitant down-regulation of IL-10 and IL-4. Furthermore, anti-leishmanial defence function (ROS) of splenocytes was observed increased in the presence of DC-delivered KMP-11 vaccination accompanied with an increased p38-MAPK signalling in vaccinated splenocytes. We summarized from our data that KMP-11 delivered through DCs has potential for eliciting protective immunity through pro-inflammatory cytokines (IFN-γ, IL-12, IL-2, TNF-α) following an up-regulation in signalling event of p38-MAPK. Therefore the study suggests a new control strategy against VL in future. >
机译:可用的报告表明, Leishmania Donovani 抗原KMP-11可能在内脏LeishManiaisis(VL)中的免疫应答调节中具有重要意义。该研究评估了通过对来自受感染的BALB / C小鼠的VL鼠突氏菌细胞呈现KMP-11抗原的疫苗前景。我们在此报告,通过骨髓衍生的树突细胞递送的KMP-11免疫会导致杀死 l。 Donovani 在感染的Balb / c小鼠中。此外,使用KMP-11作为通过DCS递送的疫苗使用的策略可以促进IFN-G,IL-12,IL-2R和TNF-α的产生,同时延长IL-10和IL-4。此外,观察到脾细胞的抗Leishmanial防御功能(ROS)在伴随的DC递送的KMP-11疫苗接种中增加,伴随着疫苗接种的脾细胞中的增加的P38-MAPK信号传导。我们总结了通过DC,通过DC的KMP-11通过促炎细胞因子(IFN-γ,IL-12,IL-2,TNF-α)在P38的信号传导事件中引发保护性免疫的可能性-mapk。因此,该研究表明,未来对VL的新控制策略。 >

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