抗铜绿假单胞菌和金黄色葡萄球菌感染的二价蛋白亚单位疫苗的研制。

IF 6.5 1区 医学 Q1 IMMUNOLOGY
Suhrid Maiti, Prolay Halder, Debaki Ranjan Howlader, Zackary K Dietz, Satabdi Biswas, Md Shafiullah Parvej, Mst Nusrat Zahan, Ti Lu, Timothy A Snider, Sean K Whittier, William D Picking, Wendy L Picking
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引用次数: 0

摘要

铜绿假单胞菌(PA)和金黄色葡萄球菌(SA)是ESKAPE病原体的成员,ESKAPE病原体是一组细菌,由于它们具有抵抗抗生素的能力,对人类健康构成威胁。已知它们可在囊性纤维化、糖尿病、伤口、肺炎和需要插管导致呼吸机相关性肺炎的危重患者等患者中引起严重感染,通常为合并症。SA和PA多药耐药的出现使得传统的抗生素治疗无效,不幸的是,没有许可的疫苗来预防MRSA或PA感染。我们已经证明,当经鼻给药(IN) L-PaF时,PA III型分泌系统(T3SS)蛋白PcrV和PopB (PaF)与LTA1(来自产肠毒素大肠杆菌的热不稳定肠毒素的活性部分)的基因融合可以保护PA。在小鼠肺定植模型中,将L-PaF配制成纳米乳(ME),以增强对临床相关PA菌株的保护性免疫反应。在SA蛋白IsdB的血红素捕获域NEAT2的加入下,产生了一种二价疫苗。二价制剂的管理保护MRSA预暴露小鼠从MRSA和PA感染。用我们的制剂接种的小鼠血清中含有很强的IgG滴度,对同源和异源PA和SA菌株具有高水平的抗噬细胞杀伤作用。此外,二价L-PaF/NEAT2制剂引起IL-17A和IL-2细胞因子的刺激。由于兔建立的PA和SA肺部感染模型更能再现人类严重急性肺炎的临床特征,因此用二价L-PaF/NEAT2制剂对兔进行免疫。所有接种疫苗的兔子都在挑战中幸存下来,而对照组却没有。这些发现表明,我们的L-PaF/ME/NEAT2制剂有潜力作为广谱疫苗对抗SA和PA感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a bivalent protein subunit vaccine against infection by Pseudomonas aeruginosa and Staphylococcus aureus.

Pseudomonas aeruginosa (PA) and Staphylococcus aureus (SA) are members of the ESKAPE pathogens, a group of bacteria that are a threat to human health due to their ability to resist antibiotics. They are known to cause severe infections, often as co-morbidities, in individuals with conditions such as people with cystic fibrosis, diabetes, wounds, pneumonia, and critically ill patients requiring intubation leading to ventilator-associated pneumonia. Emergence of multi-drug resistance in SA and PA is making traditional antibiotic treatment ineffective and unfortunately there are no licensed vaccines to prevent MRSA or PA infections. We have demonstrated that when delivered intranasally (IN) L-PaF, a genetic fusion of the PA type III secretion system (T3SS) proteins PcrV and PopB (PaF) with LTA1, the active moiety of heat-labile enterotoxin from enterotoxigenic E. coli, protects against PA. L-PaF was formulated as a nanoemulsion (ME) to increase the protective immune response against clinically relevant PA strains in a mouse lung colonization model. With the addition NEAT2, the heme capturing domain of the SA protein IsdB, a bivalent vaccine was generated. IN administration of the bivalent formulation protected MRSA pre-exposed mice from both MRSA and PA infection. Sera from mice vaccinated with our formulation contained strong IgG titers with high levels of opsonophagocytic killing of homologous and heterologous PA and SA strains. Additionally, the bivalent L-PaF/NEAT2 formulation elicited stimulation of IL-17A and IL-2 cytokines. Because established PA and SA lung infection models with rabbits better reproduce the clinical hallmarks of severe human acute pneumonia, rabbits were immunized with the bivalent L-PaF/NEAT2 formulation. All of the vaccinated rabbits survived the challenges while the controls did not. These findings demonstrate that our L-PaF/ME/NEAT2 formulation has potential as a broad-spectrum vaccine against both SA and PA infection.

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来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
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