Nagata Tomoya, Toyota Toshiaki, Ishigaki Hirohito, Ichihashi Toru, Kajino Kiichi, Kashima Yoshitaka, Itoh Yasushi, Mori Masahito, Oda Hiroshi, Yamamura Hiroyuki, Taneichi Maiko, Uchida Tetsuya, Ogasawara Kazumasa
Department of Pathology, Shiga University of Medical Science, Ohtsu 520-2192, Japan.
Vaccine. 2007 Jun 21;25(26):4914-21. doi: 10.1016/j.vaccine.2007.04.010. Epub 2007 Apr 20.
In our previous study, OVA conjugated on the surface of a liposome, we termed Oleoyl liposome, which consisted of dioleoyl phosphatidyl choline, dioleoyl phosphatidyl ethanolamine, dioleoyl phosphatidyl glycerol acid and cholesterol in a 4:3:7:2 molar ratio, induced OVA-specific IgG antibody production but not OVA-specific IgE antibody production that is detrimental to the host. Furthermore, OVA(257-264)-Oleoyl liposome elicited CTL responses in the presence of CpG and rejected E.G7 tumors in mice. In this study we tested whether a peptide-Oleoyl liposome conjugates are capable of inducing protection against viral growth. Subcutaneous inoculation of NP(366-374)-Oleoyl liposome with CpG inhibited growth of influenza viruses in lungs of mice. Thus, surface-linked liposomal peptide might serve as an effective vaccine without detrimental effects in the presence of immune potentiators.
在我们之前的研究中,卵清蛋白(OVA)偶联在脂质体表面,我们将其称为油酰脂质体,它由二油酰磷脂酰胆碱、二油酰磷脂酰乙醇胺、二油酰磷脂酰甘油酸和胆固醇按4:3:7:2的摩尔比组成,可诱导产生OVA特异性IgG抗体,但不会产生对宿主有害的OVA特异性IgE抗体。此外,OVA(257 - 264)-油酰脂质体在存在CpG的情况下引发细胞毒性T淋巴细胞(CTL)反应,并在小鼠体内排斥E.G7肿瘤。在本研究中,我们测试了肽 - 油酰脂质体偶联物是否能够诱导针对病毒生长的保护作用。皮下接种NP(366 - 374)-油酰脂质体与CpG可抑制小鼠肺部流感病毒的生长。因此,表面连接的脂质体肽在存在免疫增强剂的情况下可能作为一种有效的疫苗且无有害影响。