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研发一种新型的基于伤寒沙门氏菌和甲型副伤寒沙门氏菌外膜囊泡的两价疫苗,用于防治肠热病。

Development of a novel S. Typhi and Paratyphi A outer membrane vesicles based bivalent vaccine against enteric fever.

机构信息

Division of Bacteriology, National Institute of Cholera and Enteric Diseases, Beliaghata, Kolkata, India.

出版信息

PLoS One. 2018 Sep 14;13(9):e0203631. doi: 10.1371/journal.pone.0203631. eCollection 2018.

Abstract

Salmonella Typhi and Salmonella Paratyphi A are the leading causative agents of enteric fever which cause morbidity and mortality worldwide. Currently, there is no combination vaccine which could protect infection from both the strains. In this paper, we are focusing on the development of a novel bivalent typhoidal Outer Membrane Vesicles (OMVs) based immunogen against enteric fever. We have isolated Salmonella Typhi and Paratyphi A OMVs and also characterized OMVs associated antigens. Then we immunized adult mice with three doses of our newly formulated bivalent immunogen orally (25 μg/200 μl). After three doses of oral immunization, we found our immunogen could significantly induce humoral response. We have also found serum IgG against LPS, Vi-polysaccharide etc. OMV immunization induces CD4, CD8 and CD19 population in immunized mice spleen. It also induces Th1 and Th17-cell mediated immunity. We also found bivalent OMVs immunization can prevent more than lethal dose of heterologous Salmonella strains mediated systemic infection in adult mice model. We determined that, the protective immune responses depend on the humoral and cell-mediated immune response. Furthermore, we have evaluated the mode of protective immune response carried out by anti-OMVs antibody by significantly inhibiting bacterial motility and mucin penetration ability. Taken together, these findings suggest that our bivalent immunogen could be used as a novel candidate vaccine against enteric fever.

摘要

伤寒沙门氏菌和甲型副伤寒沙门氏菌是引起肠热病的主要病原体,在全球范围内造成发病率和死亡率。目前,尚无能够预防两种菌株感染的联合疫苗。本文专注于开发一种新型两价伤寒外膜囊泡(OMVs)免疫原,用于预防肠热病。我们已经分离出伤寒沙门氏菌和甲型副伤寒沙门氏菌的 OMVs,并对 OMVs 相关抗原进行了表征。然后,我们通过口服方式用我们新配方的两价免疫原对成年小鼠进行了三次免疫(25μg/200μl)。经过三次口服免疫后,我们发现我们的免疫原可以显著诱导体液反应。我们还发现针对 LPS、Vi-多糖等的血清 IgG。OMV 免疫可诱导免疫小鼠脾脏中的 CD4、CD8 和 CD19 群体。它还诱导 Th1 和 Th17 细胞介导的免疫。我们还发现,两价 OMVs 免疫可以预防成年小鼠模型中由异源沙门氏菌菌株介导的致死剂量的全身感染。我们确定,保护性免疫反应依赖于体液和细胞介导的免疫反应。此外,我们通过显著抑制细菌的运动性和粘蛋白穿透能力,评估了抗 OMVs 抗体所发挥的保护性免疫反应模式。综上所述,这些发现表明,我们的两价免疫原可以作为预防肠热病的新型候选疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1d7/6138408/e7d71a10e8a6/pone.0203631.g001.jpg

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