Laboratory of Microbiology and Immunology, Gifu Pharmaceutical University, Gifu, Japan.
Laboratory of Microbiology and Immunology, Gifu Pharmaceutical University, Gifu, Japan.
Vaccine. 2024 Aug 13;42(20):125975. doi: 10.1016/j.vaccine.2024.05.023. Epub 2024 May 19.
Mucosal vaccination presents a promising complement to parenteral vaccination. Bacterium-like particles (BLPs), peptidoglycan structures prepared from lactic acid bacteria, are explored as potential nasal vaccine adjuvants for respiratory infections. To date, studies on BLP-adjuvanted nasal vaccines against intestinal infections have remained limited. In this study, we demonstrated the efficacy of intranasal BLP-adjuvanted vaccination in controlling intestinal infections using the Citrobacter rodentium (C. rodentium) model in C57BL/6 mice. Intranasal vaccination of Intimin, an adhesin critical for intimate bacterial adhesion to colonic epithelial cells, combined with BLP (BLP+I) elicited robust Intimin-specific intestinal secretory IgA production, reduced bacterial load in feces and almost completely inhibited colonic hyperplasia, a characteristic symptom of C. rodentium infection in mice. Conversely, parenteral vaccination with Alhydrogel-adjuvanted Intimin failed to induce intestinal Intimin-specific IgA production, resulting in poor protection against C. rodentium infection. This underscores the pivotal role of mucosal IgA responses elicited by intranasal immunization in its protective efficacy. As this study did not delineate the precise protective mechanism conferred by BLP+I intranasal immunization against C. rodentium infection, further elucidation of the mechanisms underlying intranasal BLP+I immunization is required.
黏膜疫苗接种为肠外疫苗接种提供了一种很有前途的补充。细菌样颗粒(BLP),即从乳酸菌中提取的肽聚糖结构,被探索作为针对呼吸道感染的潜在鼻用疫苗佐剂。迄今为止,针对肠道感染的 BLP 佐剂鼻用疫苗的研究仍然有限。在这项研究中,我们使用 C57BL/6 小鼠中的柠檬酸杆菌(C. rodentium)模型,证明了鼻内 BLP 佐剂疫苗接种在控制肠道感染方面的功效。与 BLP(BLP+I)联合使用紧密素(一种对细菌与结肠上皮细胞紧密黏附至关重要的黏附素)的鼻内疫苗接种引发了强烈的紧密素特异性肠道分泌型 IgA 产生,减少了粪便中的细菌负荷,并几乎完全抑制了结肠增生,这是 C. rodentium 感染小鼠的特征症状。相反,用 Alhydrogel 佐剂的紧密素进行的肠外疫苗接种未能诱导肠道紧密素特异性 IgA 产生,导致对 C. rodentium 感染的保护作用不佳。这突显了鼻内免疫引发的黏膜 IgA 反应在其保护功效中的关键作用。由于本研究未阐明 BLP+I 鼻内免疫接种对 C. rodentium 感染的精确保护机制,因此需要进一步阐明鼻内 BLP+I 免疫接种的机制。