鼻腔给药
接种疫苗
免疫学
免疫
微生物学
免疫原性
因蒂明
医学
柠檬酸杆菌
免疫系统
生物
细菌
遗传学
细菌蛋白
大肠杆菌蛋白质类
作者
Ayato Tsujii,Keita Takahashi,Haruki Harada,Sarana Kawashima,Hina Oikawa,Hiroki Fukushima,Yuta Hayakawa,Juri Koizumi,Naoki Inoue,Tetsuo Koshizuka
出处
期刊:Vaccine
[Elsevier]
日期:2024-05-19
卷期号:42 (20): 125975-125975
标识
DOI:10.1016/j.vaccine.2024.05.023
摘要
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.
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