Vajdy Michael, Srivastava Indresh, Polo John, Donnelly John, O'Hagan Derek, Singh Manmohan
Chiron Vaccines, Emeryville, California 94608, USA.
Immunol Cell Biol. 2004 Dec;82(6):617-27. doi: 10.1111/j.1440-1711.2004.01288.x.
Almost all vaccinations today are delivered through parenteral routes. Mucosal vaccination offers several benefits over parenteral routes of vaccination, including ease of administration, the possibility of self-administration, elimination of the chance of injection with infected needles, and induction of mucosal as well as systemic immunity. However, mucosal vaccines have to overcome several formidable barriers in the form of significant dilution and dispersion; competition with a myriad of various live replicating bacteria, viruses, inert food and dust particles; enzymatic degradation; and low pH before reaching the target immune cells. It has long been known that vaccination through mucosal membranes requires potent adjuvants to enhance immunogenicity, as well as delivery systems to decrease the rate of dilution and degradation and to target the vaccine to the site of immune function. This review is a summary of current approaches to mucosal vaccination, and it primarily focuses on adjuvants as immunopotentiators and vaccine delivery systems for mucosal vaccines based on protein, DNA or RNA. In this context, we define adjuvants as protein or oligonucleotides with immunopotentiating properties co-administered with pathogen-derived antigens, and vaccine delivery systems as chemical formulations that are more inert and have less immunomodulatory effects than adjuvants, and that protect and deliver the vaccine through the site of administration. Although vaccines can be quite diverse in their composition, including inactivated virus, virus-like particles and inactivated bacteria (which are inert), protein-like vaccines, and non-replicating viral vectors such as poxvirus and adenovirus (which can serve as DNA delivery systems), this review will focus primarily on recombinant protein antigens, plasmid DNA, and alphavirus-based replicon RNA vaccines and delivery systems. This review is not an exhaustive list of all available protein, DNA and RNA vaccines, with related adjuvants and delivery systems, but rather is an attempt to highlight many of the currently available approaches in immunopotentiation of mucosal vaccines.
如今,几乎所有疫苗都是通过非肠道途径接种的。与非肠道疫苗接种途径相比,黏膜疫苗接种具有诸多优势,包括易于给药、可自行接种、消除了使用受污染针头注射的风险,以及可诱导黏膜免疫和全身免疫。然而,黏膜疫苗在到达靶免疫细胞之前,必须克服几个巨大的障碍,如显著的稀释和扩散、与大量各种活的复制细菌、病毒、惰性食物和灰尘颗粒的竞争、酶降解以及低pH值。长期以来,人们都知道通过黏膜进行疫苗接种需要强效佐剂来增强免疫原性,以及递送系统来降低稀释和降解速率,并将疫苗靶向免疫功能部位。本综述总结了当前黏膜疫苗接种的方法,主要关注作为免疫增强剂的佐剂以及基于蛋白质、DNA或RNA的黏膜疫苗的递送系统。在此背景下,我们将佐剂定义为与病原体衍生抗原共同给药的具有免疫增强特性的蛋白质或寡核苷酸,将疫苗递送系统定义为比佐剂更惰性且免疫调节作用更小的化学制剂,其可保护疫苗并将其递送至给药部位。尽管疫苗的组成可能多种多样,包括灭活病毒、病毒样颗粒和灭活细菌(它们是惰性的)、蛋白质样疫苗,以及痘病毒和腺病毒等非复制性病毒载体(它们可作为DNA递送系统),但本综述将主要关注重组蛋白抗原、质粒DNA以及基于甲病毒的复制子RNA疫苗和递送系统。本综述并非所有可用的蛋白质、DNA和RNA疫苗及其相关佐剂和递送系统的详尽列表,而是试图突出黏膜疫苗免疫增强方面目前可用的许多方法。