脂质体
磷脂酰丝氨酸
磷脂酰乙醇胺
人口
化学
双层
抗原
甘露糖受体
磷脂酰胆碱
生物
细胞生物学
生物物理学
体外
生物化学
免疫学
磷脂
医学
膜
巨噬细胞
环境卫生
作者
Camilla Foged,Carmen Arigita,Anne Sundblad,Wim Jiskoot,Gert Storm,Sven Frøkjær
出处
期刊:Vaccine
[Elsevier]
日期:2003-12-06
卷期号:22 (15-16): 1903-1913
被引量:206
标识
DOI:10.1016/j.vaccine.2003.11.008
摘要
Vaccine efficacy might be improved by exploiting the potent antigen presenting properties of dendrite cells (DCs), since their ability to stimulate specific major histocompatibility complex-restricted immune responses has been well documented during the recent years. In that light, we investigated how the interaction of antigen-containing liposomes with DCs was affected by the bilayer composition. Monocyte-derived human DCs and murine bone marrow-derived DCs were analysed and compared upon in vitro incubation with liposomes by flow cytometry and confocal microscopy. Anionic liposomes with a bilayer composition of phosphatidylcholine, cholesterol and phosphatidylglycerol or phosphatidylserine interacted with a limited fraction of the total DC population in case of both DC types. Inclusion of mannosylated phosphatidylethanolamine (Man-PE) for targeting to the mannose receptor (MR) increased the interaction of negatively charged liposomes with both human and murine DCs. This increase could be blocked in human DCs by addition of the polysaccharide mannan indicating that uptake might be mediated by the mannose receptor. Cationic liposomes containing trimethyl ammonium propane interacted with a very high percentage of both DC types and could be detected in high amounts intracellularly. In conclusion, liposome bilayer composition has an important effect on interaction with DCs and might be critical for the vaccination outcome.
科研通智能强力驱动
Strongly Powered by AbleSci AI