Perrin P, Thibodeau L, Sureau P
Vaccine. 1985 Sep;3(3):325-32. doi: 10.1016/s0264-410x(85)90224-5.
Rabies immunosomes (glycoprotein anchored on pre-formed liposomes) have been prepared in order to study their structural, biological and immunological properties. The glycoprotein molecules appear to have the same orientation on the immunosome as on the viral particle: (1) electron microscopy analysis shows particles of 40 to 70 nm with spikes protruding outward, (2) one particular epitope shows the same accessibility to a neutralizing monoclonal antibody as on the viral particle. When injected into animals, rabies immunosomes are cleared from the organism by a process different from that for the liposomes used to anchor the glycoprotein: a higher rate of transition through the spleen is observed with immunosomes than with purified glycoprotein or liposomes. Immunosomes induce high levels of neutralizing antibodies and protect animals against challenge with virulent strains. This protective activity is not altered after several months of storage at 4 degrees C. Furthermore, rabies immunosomes were shown to be efficient in post-exposure treatment of laboratory animals that had been experimentally infected with a lethal dose of a rabies wild strain.
为了研究其结构、生物学和免疫学特性,制备了狂犬病免疫脂质体(糖蛋白锚定在预先形成的脂质体上)。糖蛋白分子在免疫脂质体上的取向似乎与在病毒颗粒上相同:(1)电子显微镜分析显示颗粒大小为40至70纳米,有向外突出的刺突;(2)一个特定的表位对中和单克隆抗体的可及性与在病毒颗粒上相同。当注入动物体内时,狂犬病免疫脂质体通过与用于锚定糖蛋白的脂质体不同的过程从机体中清除:与纯化的糖蛋白或脂质体相比,免疫脂质体通过脾脏的转运速率更高。免疫脂质体可诱导高水平的中和抗体,并保护动物免受强毒株的攻击。在4℃储存几个月后,这种保护活性不会改变。此外,狂犬病免疫脂质体在对实验感染致死剂量狂犬病野毒株的实验动物进行暴露后治疗中显示出有效性。