假结核耶尔森菌
酵母
酿酒酵母
体外
整合素
耶尔森尼亚
小肠结肠炎耶尔森菌
微生物学
化学
体内
细胞
细胞生物学
重组DNA
抗原
生物
生物化学
免疫学
细菌
毒力
遗传学
基因
作者
Elisabeth E. Kenngott,Ruth Kiefer,Nicole Schneider‐Daum,Alf Hamann,Marc Schneider,Manfred Schmitt,Frank Breinig
标识
DOI:10.1016/j.jconrel.2015.12.054
摘要
The effective targeting and subsequent binding of particulate carriers to M cells in Peyer's patches of the gut is a prerequisite for the development of oral delivery systems. We have established a novel carrier system based on cell surface expression of the β1-integrin binding domain of invasins derived from Yersinia enterocolitica and Yersinia pseudotuberculosis on the yeast Saccharomyces cerevisiae. All invasin derivatives were shown to be effectively expressed on the cell surface and recombinant yeast cells showed improved binding to both human HEp-2 cells and M-like cells in vitro. Among the different derivatives tested, the integrin-binding domain of Y. enterocolitica invasin proved to be the most effective and was able to target Peyer's patches in vivo. In conclusion, cell surface-modified yeasts might provide a novel bioadhesive, eukaryotic carrier system for efficient and targeted delivery of either antigens or drugs via the oral route.
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