首页> 外文OA文献 >The Protective Effect of the Mycobacterium bovis BCG Vaccine Is Increased by Coadministration with the Mycobacterium tuberculosis 72-Kilodalton Fusion Polyprotein Mtb72F in M. tuberculosis-Infected Guinea Pigs
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The Protective Effect of the Mycobacterium bovis BCG Vaccine Is Increased by Coadministration with the Mycobacterium tuberculosis 72-Kilodalton Fusion Polyprotein Mtb72F in M. tuberculosis-Infected Guinea Pigs

机译:与结核分枝杆菌72-Kilodalton融合多蛋白Mtb72F并用对结核分枝杆菌感染的豚鼠增加牛分枝杆菌卡介苗的保护作用

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摘要

A tuberculosis vaccine candidate consisting of a 72-kDa polyprotein or fusion protein based upon the Mtb32 and Mtb39 antigens of Mycobacterium tuberculosis and designated Mtb72F was tested for its protective capacity as a potential adjunct to the Mycobacterium bovis BCG vaccine in the mouse and guinea pig models of this disease. Formulation of recombinant Mtb72F (rMtb72F) in an AS02A adjuvant enhanced the Th1 response to BCG in mice but did not further reduce the bacterial load in the lungs after aerosol challenge infection. In the more stringent guinea pig disease model, rMtb72F delivered by coadministration with BCG vaccination significantly improved the survival of these animals compared to BCG alone, with some animals still alive and healthy in their appearance at >100 weeks post-aerosol challenge. A similar trend was observed with guinea pigs in which BCG vaccination was boosted by DNA vaccination, although this increase was not statistically significant due to excellent protection conferred by BCG alone. Histological examination of the lungs of test animals indicated that while BCG controls eventually died from overwhelming lung consolidation, the majority of guinea pigs receiving BCG mixed with rMtb72F or boosted twice with Mtb72F DNA had mostly clear lungs with minimal granulomatous lesions. Lesions were still prominent in guinea pigs receiving BCG and the Mtb72F DNA boost, but there was considerable evidence of lesion healing and airway remodeling and reestablishment. These data support the hypothesis that the coadministration or boosting of BCG vaccination with Mtb72F may limit the lung consolidation seen with BCG alone and may promote lesion resolution and healing. Collectively, these data suggest that enhancing BCG is a valid vaccination strategy for tuberculosis that is worthy of clinical evaluation.
机译:在小鼠和豚鼠模型中,测试了一种由72kDa多聚蛋白或基于结核分枝杆菌Mtb32和Mtb39抗原的融合蛋白组成并命名为Mtb72F的结核疫苗候选物作为牛分枝杆菌BCG疫苗的潜在佐剂的保护能力。这种疾病。在AS02A佐剂中配制重组Mtb72F(rMt​​b72F)增强了小鼠对BCG的Th1反应,但并未进一步降低气溶胶激发感染后肺中的细菌载量。在更严格的豚鼠疾病模型中,与单独的BCG相比,与BCG疫苗共同给药所递送的rMtb72F显着提高了这些动物的存活率,其中一些动物在气雾剂攻击后> 100周时其外观仍然存活且健康。在豚鼠中观察到了类似的趋势,其中通过DNA疫苗接种加强了BCG疫苗接种,尽管由于单独使用BCG给予了出色的保护,这种增加在统计上并不显着。对试验动物的肺进行组织学检查表明,虽然BCG对照最终因压倒性肺部固结死亡,但大多数接受了BCG混入rMtb72F或用Mtb72F DNA加强免疫的豚鼠的肺大部分呈透明性,肉芽肿性病变最小。在接受卡介苗和Mtb72F DNA增强的豚鼠中,病变仍很突出,但是有相当多的证据表明病变可以愈合,气道重塑和重建。这些数据支持以下假设,即与Mtb72F共同施用或加强BCG疫苗接种可能会限制仅使用BCG所见的肺部巩固,并可能促进病变消退和愈合。总的来说,这些数据表明,增强卡介苗是一种有效的结核病疫苗接种策略,值得临床评估。

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