Cheng Jing-Yan, Huang Hang-Ning, Tseng Wen-Chi, Li Tsung-Lin, Chan Yi-Lin, Cheng Kai-Chun, Wu Chang-Jer
Department of Food Science, National Taiwan Ocean University, Keelung, Taiwan; Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.
J Control Release. 2009 May 5;135(3):242-9. doi: 10.1016/j.jconrel.2009.01.014. Epub 2009 Jan 29.
Skin, the biggest organ of human body, contains antigen presenting cells such as Langerhans cells (LCs) that modulate various immune responses. The skin therefore is an ideal venue to effect the transcutaneous immunization (TCI). Most current immunization procedures make use of needles and syringes for vaccine administration, which however have raised many safety concerns. To overcome the stratum corneum barrier of the skin without carrying out any skin penetration, cationic liposomes, DC-Chol/DOPE and DOTAP, were employed as vehicles for the transdermal antigen DNA delivery in this study. The optimal ratio of liposomes to DNAs for maximal transfection efficiency was determined to be 5:1 (w/w) for both formulas in BHK-21 cell transfection assays. This ratio was applied to lipoplex in tests on the dorsal skin of hair-removed mice. Reporter genes were found expressed in epidermis and spleen over 3 days. C3H/HeN mice transcutaneously immunized with the skin patch containing liposome-pCJ-3/ME (lipoplex-patch; pCJ-3/ME expressing the whole membrane and envelope protein genes of Japanese encephalitis virus (JEV)) can induce effective and protective antibodies against the infection with 50 times the 50% lethal dose (LD(50)) of JEV. The developed lipoplex-patch DNA vaccines have proven to be simple and noninvasive, by which the antibodies incurred provide marked therapeutic effects in test animals.
皮肤是人体最大的器官,含有抗原呈递细胞,如调节各种免疫反应的朗格汉斯细胞(LCs)。因此,皮肤是进行经皮免疫(TCI)的理想场所。目前大多数免疫程序使用针头和注射器进行疫苗接种,然而这引发了许多安全问题。为了在不穿透皮肤的情况下克服皮肤角质层屏障,本研究采用阳离子脂质体DC-Chol/DOPE和DOTAP作为经皮抗原DNA递送的载体。在BHK-21细胞转染试验中,两种配方的脂质体与DNA的最佳比例(以实现最大转染效率)均确定为5:1(w/w)。该比例应用于脱毛小鼠背部皮肤的脂质体复合物测试。在3天内,在表皮和脾脏中发现报告基因表达。用含有脂质体-pCJ-3/ME(脂质体复合物贴片;pCJ-3/ME表达日本脑炎病毒(JEV)的全膜和包膜蛋白基因)的皮肤贴片经皮免疫C3H/HeN小鼠,可诱导产生针对50倍50%致死剂量(LD50)JEV感染的有效保护性抗体。已证明所开发的脂质体复合物贴片DNA疫苗简单且无创,其所产生的抗体在试验动物中具有显著的治疗效果。