Suppr超能文献

用包裹流感病毒抗原的类蛋白微球对大鼠进行口服免疫。

Oral immunization of rats with proteinoid microspheres encapsulating influenza virus antigens.

作者信息

Santiago N, Milstein S, Rivera T, Garcia E, Zaidi T, Hong H, Bucher D

机构信息

Emisphere Technologies, Inc., Hawthorne, New York 10532.

出版信息

Pharm Res. 1993 Aug;10(8):1243-7. doi: 10.1023/a:1018992924025.

Abstract

Influenza virus antigen microspheres were prepared by a pH-dependent process using a protein-like polymer (proteinoid) made by thermal condensation of amino acids. The efficacy of these preparations to induce specific IgG responses when used as oral vaccines in rats was evaluated. A single enteric dose of M1 entrapped in proteinoid microspheres was able to induce a significant IgG response to M1 as early as 2 weeks postdosing, while rats dosed orally with the same M1 total dose (no microspheres) showed no detectable antibody response. An unencapsulated hemagglutinin and neuraminidase (HA-NA) preparation induced a moderate anti HA-NA IgG response. A single enteric dose of HA-NA spheres induced a response in 33% of the rats; this response was up to eight times higher than that observed in the rats dosed with unencapsulated antigen.

摘要

流感病毒抗原微球是通过一个pH依赖过程制备的,该过程使用了由氨基酸热缩合制成的类蛋白聚合物(类蛋白质)。评估了这些制剂在大鼠中用作口服疫苗时诱导特异性IgG反应的功效。单次肠溶剂量包裹在类蛋白质微球中的M1早在给药后2周就能诱导对M1产生显著的IgG反应,而口服相同总剂量M1(无微球)的大鼠则未显示可检测到的抗体反应。未封装的血凝素和神经氨酸酶(HA-NA)制剂诱导了中等程度的抗HA-NA IgG反应。单次肠溶剂量的HA-NA微球在33%的大鼠中诱导了反应;该反应比给予未封装抗原的大鼠中观察到的反应高八倍。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验