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包封抗原的 archaeosomes 用于口服疫苗传递。

Archaeosomes with encapsulated antigens for oral vaccine delivery.

机构信息

Department of Cell Biology, Nanjing Medical University, Nanjing 210029, PR China.

出版信息

Vaccine. 2011 Jul 18;29(32):5260-6. doi: 10.1016/j.vaccine.2011.05.015. Epub 2011 May 24.

Abstract

Traditional phosphodiester lipid vesicles (liposomes) are not stable and could be easily degraded in the gastrointestinal (GI) tract. We prepared a novel lipid based oral delivery system: archaeosomes, made of the polar lipid fraction E (PLFE) extracted from Sulfolobus acidocaldarius, and tested their immunogenic potentials as oral vaccine delivery vehicles. Our study showed that the archaeosomes had significant superior stability in simulated gastric and intestinal fluids, and would help fluorescent labeled antigens to reside longer time in the GI tract after oral administration. The resulted immune responses against model antigen ovalbumin (OVA) were greatly improved, eliciting substantial IgG response systemically as well as IgA response mucosally. In addition, the archaeosomes also facilitated antigen specific CD8(+) T cell proliferation. These data indicate that archaeosomes may be a potential vaccine carrier and adjuvant for effective oral immunization.

摘要

传统的磷酸二酯脂质体(脂质体)不稳定,在胃肠道(GI)中容易降解。我们制备了一种新型的基于脂质的口服给药系统:来源于极端酸性热泉古菌(Sulfolobus acidocaldarius)的极性脂质提取物(PLFE)制成的 archaeosomes,并测试了它们作为口服疫苗传递载体的免疫原性潜力。我们的研究表明,archaeosomes 在模拟胃液和肠液中具有显著优越的稳定性,并有助于荧光标记的抗原在口服给药后在胃肠道中停留更长时间。对模型抗原卵清蛋白(OVA)的产生的免疫反应得到了极大的改善,引起了全身性的大量 IgG 反应以及粘膜的 IgA 反应。此外,archaeosomes 还促进了抗原特异性 CD8(+)T 细胞的增殖。这些数据表明 archaeosomes 可能是一种有效的口服免疫的潜在疫苗载体和佐剂。

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