Immunization with Escherichia coli Outer Membrane Vesicles Protects Bacteria-Induced Lethality via Th1 and Th17 Cell Responses

免疫 细菌外膜 免疫系统 微生物学 大肠杆菌 细菌 生物 免疫 过继性细胞移植 接种疫苗 免疫学 T细胞 基因 生物化学 遗传学
作者
Oh Youn Kim,Bok Sil Hong,Kyong‐Su Park,Yae Jin Yoon,Seng Jin Choi,W. Lee,Tae‐Young Roh,Jan Lötvall,Yoon‐Keun Kim,Yong Song Gho
出处
期刊:Journal of Immunology [American Association of Immunologists]
卷期号:190 (8): 4092-4102 被引量:157
标识
DOI:10.4049/jimmunol.1200742
摘要

Abstract Outer membrane vesicles (OMVs), secreted from Gram-negative bacteria, are spherical nanometer-sized proteolipids enriched with outer membrane proteins. OMVs, also known as extracellular vesicles, have gained interests for use as nonliving complex vaccines and have been examined for immune-stimulating effects. However, the detailed mechanism on how OMVs elicit the vaccination effect has not been studied extensively. In this study, we investigated the immunological mechanism governing the protective immune response of OMV vaccines. Immunization with Escherichia coli–derived OMVs prevented bacteria-induced lethality and OMV-induced systemic inflammatory response syndrome. As verified by adoptive transfer and gene-knockout studies, the protective effect of OMV immunization was found to be primarily by the stimulation of T cell immunity rather than B cell immunity, especially by the OMV-Ag–specific production of IFN-γ and IL-17 from T cells. By testing the bacteria-killing ability of macrophages, we also demonstrated that IFN-γ and IL-17 production is the main factor promoting bacterial clearances. Our findings reveal that E. coli–derived OMV immunization effectively protects bacteria-induced lethality and OMV-induced systemic inflammatory response syndrome primarily via Th1 and Th17 cell responses. This study therefore provides a new perspective on the immunological detail regarding OMV vaccination.
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