Xu Jin, Ding Yunzhen, Yang Yi
Pediatric Institute, Children's Hospital, Fudan University, Shanghai, China.
Viral Immunol. 2008 Dec;21(4):483-9. doi: 10.1089/vim.2008.0044.
Respiratory syncytial virus (RSV) is one of the principal causes of bronchiolitis and pneumonia in young children, and currently there is no safe and effective vaccine. DNA vaccines encoding RSV surface glycoproteins are one option being examined. We evaluated the topical delivery of transfersome encapsulated DNA vaccine for its ability to confer protection against RSV challenge in mice and to determine whether such delivery could induce strong and specific immunity against RSV. After topical vaccination with a transfersome encapsulated RSV-F DNA, both RSV-specific mucosal antibody response and IFN-gamma-producing cells were detected. Intramuscular vaccination of naked RSV-F DNA only induced a significant anti-RSV IgG antibody response but no remarkable sIgA antibody and virus-specific cellular activity. Lungs from mice receiving topical vaccination had fewer histopathologic anomalies after RSV challenge than did mice receiving intramuscular vaccination or controls. Immunization with transfersome encapsulated F gene encoding DNA induces mucosal and cellular immune responses in mice that appear to produce protective immunity against respiratory syncytial virus.
呼吸道合胞病毒(RSV)是幼儿毛细支气管炎和肺炎的主要病因之一,目前尚无安全有效的疫苗。编码RSV表面糖蛋白的DNA疫苗是正在研究的一种选择。我们评估了脂质体包裹的DNA疫苗经局部给药后在小鼠中抵御RSV攻击的能力,并确定这种给药方式是否能诱导针对RSV的强大而特异性的免疫反应。在用脂质体包裹的RSV-F DNA进行局部疫苗接种后,检测到了RSV特异性黏膜抗体反应和产生γ干扰素的细胞。单纯肌内接种裸露的RSV-F DNA仅诱导出显著的抗RSV IgG抗体反应,但没有明显的分泌型IgA抗体和病毒特异性细胞活性。RSV攻击后,接受局部疫苗接种的小鼠肺部的组织病理学异常比接受肌内疫苗接种的小鼠或对照组更少。用脂质体包裹的编码F基因的DNA进行免疫可在小鼠中诱导黏膜和细胞免疫反应,这似乎能产生针对呼吸道合胞病毒的保护性免疫。