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首页> 外文期刊>Vaccine >Recombinant L7/L12 protein entrapping PLGA (poly lactide-co-glycolide) micro particles protect BALB/c mice against the virulent B. abortus 544 infection
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Recombinant L7/L12 protein entrapping PLGA (poly lactide-co-glycolide) micro particles protect BALB/c mice against the virulent B. abortus 544 infection

机译:包埋PLGA(聚丙交酯-共-乙交酯)微粒的重组L7 / L12蛋白可保护BALB / c小鼠免受强力流产双歧杆菌544感染

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摘要

Brucella abortus is the etiologic agent of Brucellosis, a zoonotic infection affecting a wide range of animals. It is a highly infectious disease of pandemic potential reporting over 500,000 new human cases annually. Till date, there is no reported vaccine for humans and the available animal vaccines are unsafe, therefore a safe and effective subunit vaccine is highly sought for. In this study, we have evaluated rL7/L12 protein encapsulated in microparticles of PLGA (85:15), a biocompatible and biodegradable polymer approved by FDA for human use. In this work, BALB/c mice have been immunized with rL7/L12 entrapped in microparticles in a prime-boost regimen. Further, evaluation of the immunogenicity of the formulation showed that the IgG antibody titre reached a maxima of 2.2 x 10(5) (p value 0.0001 v/s control) after the injection of the booster dose. A mixed IgG isotype profile (IgG1/IgG2a) indicated the stimulation of both the cellular as well as humoral immunity which has increased parallely and gradually since the first immunization. High levels of IFN-gamma, 815 +/- 55 pg/ml were recorded depicting an optimal elicitation of the cellular wing of immunity leading to clearance of splenic bacteria upto 1.69 log units. (C) 2015 Elsevier Ltd. All rights reserved.
机译:流产布鲁氏菌是布鲁氏菌病的病原体,布鲁氏菌病是一种人畜共患的感染,影响多种动物。它是一种具有高度传染性的大流行潜力疾病,每年报告超过500,000例新人类病例。迄今为止,还没有针对人类的疫苗的报道,并且可用的动物疫苗是不安全的,因此,人们强烈寻求一种安全有效的亚单位疫苗。在这项研究中,我们评估了封装在PLGA(85:15)微粒中的rL7 / L12蛋白,PLGA是FDA批准用于人类的生物相容性和生物降解性聚合物。在这项工作中,BALB / c小鼠已经用初免-加强疗法中包裹在微粒中的rL7 / L12进行了免疫。此外,对制剂的免疫原性的评估表明,在注射加强剂量后,IgG抗体的效价最高达到2.2 x 10(5)(p值0.0001 v / s对照)。混合的IgG同种型谱(IgG1 / IgG2a)表明,细胞免疫和体液免疫均受到刺激,自首次免疫以来,这种免疫平行和逐渐增强。记录到高水平的IFN-γ,815 +/- 55 pg / ml,描绘了对细胞翼免疫力的最佳诱导,导致高达1.69 log单位的脾细菌清除。 (C)2015 Elsevier Ltd.保留所有权利。

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