Zhang Haochi, Sheng Shouxin, Li Chunhe, Bao Xuemei, Zhao Lixia, Chen Jian, Guan Pingyuan, Li Xiaoyan, Pan Na, Liang Yanchen, Wang Xueqi, Sun Jingmin, Wang Xiao
State Key Laboratory of Reproductive Regulation & Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot, P.R. China.
The Spirit Jinyu Biological Pharmaceutical Co. Ltd, Hohhot, Inner Mongolia, China.
PLoS Pathog. 2024 Nov 18;20(11):e1012696. doi: 10.1371/journal.ppat.1012696. eCollection 2024 Nov.
Respiratory infections caused by Pseudomonas aeruginosa are a major health problem globally. Current treatment for P. aeruginosa infections relies solely on antibiotics, but the rise of antibiotic-resistant strains necessitates an urgent need for a protective vaccine. Traditional parenteral vaccines, despite employing potent adjuvants aimed at serotype-dependent immunity, often fail to elicit the desired mucosal immune response. Thus, developing vaccines that target both localized mucosal and systemic immune responses represents a promising direction for future research on P. aeruginosa vaccination. In this study, we explored EPS301, the exopolysaccharide derived from the lung microbiota strain Lactobacillus plantarum WXD301, which exhibits excellent self-assembly properties, enabling the formation of homogeneous nanoparticles when encapsulating recombinant PcrV of P. aeruginosa, designated as EPS301@rPcrV. Notably, the EPS301 vector effectively enhanced antigen adhesion to the nasal and pulmonary mucosal tissues and prolonged antigen retention. Moreover, EPS301@rPcrV provided effective and sustained protection against P. aeruginosa pneumonia, surpassing the durability achieved with the "gold standard" cholera toxin adjuvant. The EPS301-adjuvanted vaccine formulation elicited robust mucosal IgA and Th17/γδ17 T cell responses, which exceeded those induced by the CTB-adjuvanted vaccination and were sustained for over 112 days. Additionally, Th 17 and γδ 17 resident memory T cells induced by EPS301@rPcrV were crucial for protection against P. aeruginosa challenge. Intriguingly, IL-17A knockout mice exhibited lower survival rates, impaired bacterial clearance ability, and exacerbated lung tissue damage upon EPS301 adjuvanted vaccination against P. aeruginosa-induced pneumonia, indicating an IL-17A-dependent protective mechanism. In conclusion, our findings provided direct evidence that EPS301@rPcrV mucosal vaccine is a promising candidate for future clinical application against P. aeruginosa-induced pulmonary infection.
铜绿假单胞菌引起的呼吸道感染是全球主要的健康问题。目前针对铜绿假单胞菌感染的治疗仅依赖抗生素,但抗生素耐药菌株的出现迫切需要一种保护性疫苗。传统的肠胃外疫苗,尽管使用了旨在引发血清型依赖性免疫的强效佐剂,但往往无法引发所需的黏膜免疫反应。因此,开发针对局部黏膜和全身免疫反应的疫苗是未来铜绿假单胞菌疫苗研究的一个有前景的方向。在本研究中,我们探索了EPS301,它是从肺部微生物群菌株植物乳杆菌WXD301衍生而来的胞外多糖,具有出色的自组装特性,在包裹铜绿假单胞菌的重组PcrV时能够形成均匀的纳米颗粒,命名为EPS301@rPcrV。值得注意的是,EPS301载体有效增强了抗原对鼻和肺黏膜组织的粘附,并延长了抗原滞留时间。此外,EPS301@rPcrV对铜绿假单胞菌肺炎提供了有效且持久的保护,超过了用“金标准”霍乱毒素佐剂所达到的耐久性。EPS301佐剂疫苗配方引发了强大的黏膜IgA和Th17/γδ17 T细胞反应,超过了CTB佐剂疫苗诱导的反应,并持续超过112天。此外,由EPS301@rPcrV诱导的Th 17和γδ 17驻留记忆T细胞对于抵抗铜绿假单胞菌攻击至关重要。有趣的是,IL-17A基因敲除小鼠在接受EPS301佐剂疫苗接种以预防铜绿假单胞菌诱导的肺炎后,存活率较低,细菌清除能力受损,肺组织损伤加剧,表明存在一种依赖IL-17A 的保护机制。总之,我们的研究结果提供了直接证据,表明EPS301@rPcrV黏膜疫苗是未来临床应用中对抗铜绿假单胞菌引起的肺部感染的有前景的候选疫苗。