首页> 外文期刊>Clinical and vaccine immunology: CVI >Vaccination with Leptospiral Outer Membrane Lipoprotein LipL32 Reduces Kidney Invasion of Leptospira interrogans Serovar Canicola in Hamsters
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Vaccination with Leptospiral Outer Membrane Lipoprotein LipL32 Reduces Kidney Invasion of Leptospira interrogans Serovar Canicola in Hamsters

机译:钩端螺旋体外膜脂蛋白LipL32的疫苗接种减少了肾脏中钩端螺旋体问号血清型Canicola的侵袭。

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The Leptospira interrogans vaccines currently available are serovar specific and require regular booster immunizations to maintain protection of the host. In addition, a hamster challenge batch potency test is necessary to evaluate these vaccines prior to market release, requiring the use of a large number of animals, which is ethically and financially undesirable. Our previous work showed that the N terminus of the outer membrane protein LipL32 was altered in Leptospira interrogans serovar Canicola vaccines that fail the hamster challenge test, suggesting that it may be involved in the protective immune response. The aim of this study was to determine if vaccination with LipL32 protein alone could provide a protective response against challenge with L. interrogans serovar Canicola to hamsters. Recombinant LipL32, purified from an Escherichia coli expression system, was assessed for protective immunity in five groups of hamsters (n = 5) following a challenge with the virulent L. interrogans serovar Canicola strain Kito as a challenge strain. However, no significant survival against the L. interrogans serovar Canicola challenge was observed compared to that of unvaccinated negative controls. Subsequent histological analysis revealed reduced amounts of L. interrogans in the kidneys from the hamsters vaccinated with recombinant LipL32 protein prior to challenge; however, no significant survival against the L. interrogans serovar Canicola challenge was observed compared to that of unvaccinated negative controls. This finding corresponded to a noticeably reduced severity of renal lesions. This study provides evidence that LipL32 is involved in the protective response against L. interrogans serovar Canicola in hamsters and is the first reported link to LipL32-induced protection against kidney invasion.
机译:当前可用的问号钩端螺旋体疫苗是血清型特异性的,需要定期加强免疫以维持对宿主的保护。另外,仓鼠挑战分批效力测试对于在市场发布之前评估这些疫苗是必需的,需要使用大量动物,这在伦理和经济上都是不希望的。我们以前的工作表明,在未能通过仓鼠攻击试验的问号钩端螺旋体血清型Canicola疫苗中,外膜蛋白LipL32的N末端发生了改变,表明它可能参与了保护性免疫应答。这项研究的目的是确定单独用LipL32蛋白疫苗接种是否可以提供保护作用,以抵抗问号L. intereroans血清型Canicola对仓鼠的攻击。在用强壮的问号L. interrogans血清型卡尼科拉菌株Kito攻击后,评估了从大肠杆菌表达系统纯化的重组LipL32在五组仓鼠( n = 5)中的保护性免疫力。 。然而,与未接种的阴性对照相比,没有观察到抗询问人血清型卡尼索拉攻击的显着存活。随后的组织学分析显示,攻击前接种重组LipL32蛋白的仓鼠肾脏中的询问乳杆菌数量减少。然而,与未接种疫苗的阴性对照相比,没有观察到抗询问人血清型卡尼索拉挑战的存活率。这一发现与肾脏病变的严重程度明显降低相对应。这项研究提供的证据表明,LipL32参与了仓鼠对问号乳酸杆菌血清Canicola的保护反应,并且是首次报道与LipL32诱导的针对肾脏侵袭的保护有关。

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