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混合黏膜-肠外免疫接种广泛保守的致病性大肠杆菌抗原 SslE 可诱导强大的黏膜和全身免疫,而不影响小鼠肠道微生物群。

Mixed mucosal-parenteral immunizations with the broadly conserved pathogenic Escherichia coli antigen SslE induce a robust mucosal and systemic immunity without affecting the murine intestinal microbiota.

机构信息

GSK, Siena, Italy; Université Clermont Auvergne, INRA, UMR454 MEDiS, 63000 Clermont-Ferrand, France.

GSK, Siena, Italy.

出版信息

Vaccine. 2019 Jan 7;37(2):314-324. doi: 10.1016/j.vaccine.2018.10.008. Epub 2018 Nov 30.

Abstract

Emergence and dissemination of multidrug resistance among pathogenic Escherichia coli have posed a serious threat to public health across developing and developed countries. In combination with a flexible repertoire of virulence mechanisms, E. coli can cause a vast range of intestinal (InPEC) and extraintestinal (ExPEC) diseases but only a very limited number of antibiotics still remains effective against this pathogen. Hence, a broad spectrum E. coli vaccine could be a promising alternative to prevent the burden of such diseases, while offering the potential for covering against several InPEC and ExPEC at once. SslE, the Secreted and Surface-associated Lipoprotein of E. coli, is a widely distributed protein among InPEC and ExPEC. SslE functions ex vivo as a mucinase capable of degrading mucins and reaching the surface of mucus-producing epithelial cells. SslE was identified by reverse vaccinology as a protective vaccine candidate against an ExPEC murine model of sepsis, and further shown to be cross-effective against other ExPEC and InPEC models of infection. In this study, we aimed to gain insight into the immune response to antigen SslE and identify an immunization strategy suited to generate robust mucosal and systemic immune responses. We showed, by analyzing T cell and antibody responses, that mice immunized with SslE via an intranasal prime followed by two intramuscular boosts developed an enhanced overall immune response compared to either intranasal-only or intramuscular-only protocols. Importantly, we also report that this regimen of immunization did not impact the richness of the murine gut microbiota, and mice had a comparable cecal microbial composition, whether immunized with SslE or PBS. Collectively, our findings further support the use of SslE in future vaccination strategies to effectively target both InPEC and ExPEC while not perturbing the resident gut microbiota.

摘要

产肠毒素大肠杆菌(Escherichia coli)中多重耐药性的出现和传播对发展中国家和发达国家的公共卫生都构成了严重威胁。大肠杆菌结合了灵活多样的毒力机制,可以引起广泛的肠道(InPEC)和肠道外(ExPEC)疾病,但只有非常有限的抗生素仍然对这种病原体有效。因此,广谱大肠杆菌疫苗可能是预防此类疾病负担的一种有前途的替代方法,同时有可能同时预防多种 InPEC 和 ExPEC。SslE 是大肠杆菌的分泌和表面相关脂蛋白,在 InPEC 和 ExPEC 中广泛分布。SslE 在体外作为粘蛋白酶发挥作用,能够降解粘蛋白并到达产生粘蛋白的上皮细胞表面。SslE 通过反向疫苗学被鉴定为一种针对 ExPEC 败血症小鼠模型的保护性疫苗候选物,并且进一步显示对其他 ExPEC 和 InPEC 感染模型具有交叉有效性。在这项研究中,我们旨在深入了解针对抗原 SslE 的免疫反应,并确定一种适合产生强大粘膜和全身免疫反应的免疫策略。通过分析 T 细胞和抗体反应,我们表明,通过鼻内初免然后进行两次肌肉内加强免疫接种 SslE 的小鼠与仅鼻内或仅肌肉内免疫接种的小鼠相比,产生了增强的整体免疫反应。重要的是,我们还报告称,这种免疫方案不会影响小鼠肠道微生物群的丰富度,并且无论用 SslE 还是 PBS 免疫接种,小鼠的盲肠微生物组成都具有可比性。总的来说,我们的研究结果进一步支持在未来的疫苗接种策略中使用 SslE,以有效地针对 InPEC 和 ExPEC,同时不干扰常驻肠道微生物群。

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