Department of Molecular Genetics and Microbiology, University of New Mexico, Albuquerque, NM 87131, United States.
Vaccine. 2011 Jun 20;29(28):4584-92. doi: 10.1016/j.vaccine.2011.04.051. Epub 2011 May 5.
The induction of mucosal immune responses in the genital tract may be important for increasing the effectiveness of vaccines for sexually transmitted infections (STIs). In this study, we asked whether direct immunization of the mouse genital tract with a non-replicating virus-like particle (VLP)-based vaccine could induce local mucosal as well as systemic antibody responses. Using VLPs derived from two bacteriophages, Qβ and PP7, and from a mammalian virus that normally infects the genital tract, human papillomavirus (HPV), we show that intravaginal aerosol administration of VLPs can induce high titer IgG and IgA antibodies in the female genital tract as well as IgG in the sera. Using a mouse model for HPV infection, we show that intravaginal immunization with either HPV type 16 VLPs or with PP7 bacteriophage VLPs displaying a peptide derived from the HPV minor capsid protein L2 could protect mice from genital infection with an HPV16 pseudovirus. These results provide a general method for inducing genital mucosal and systemic antibody responses using VLP-based immunogens.
诱导生殖道黏膜免疫反应对于提高针对性传播感染(STI)的疫苗的有效性可能非常重要。在这项研究中,我们探讨了是否可以通过直接将非复制型病毒样颗粒(VLP)疫苗免疫小鼠生殖道,来诱导局部黏膜和全身抗体反应。我们使用来自两种噬菌体(Qβ和 PP7)和一种通常感染生殖道的哺乳动物病毒(人乳头瘤病毒(HPV)的 VLP 进行研究,结果表明,阴道内气溶胶给予 VLP 可以诱导生殖道中高滴度的 IgG 和 IgA 抗体以及血清中的 IgG。我们利用 HPV 感染的小鼠模型,发现阴道内免疫接种 HPV16 VLP 或展示 HPV 次要衣壳蛋白 L2 衍生肽的 PP7 噬菌体 VLP,均可以保护小鼠免受 HPV16 假病毒的生殖道感染。这些结果为使用 VLP 免疫原诱导生殖道黏膜和全身抗体反应提供了一种通用方法。