Institut de Biologie et Chimie des Protéines, FRE 3310 CNRS University of Lyon 1, IFR128 Biosciences Lyon-Gerland, 7 passage du Vercors, 69367 Lyon cedex 07, France.
Vaccine. 2012 Jan 5;30(2):142-54. doi: 10.1016/j.vaccine.2011.11.003. Epub 2011 Nov 12.
Mucosal surfaces are the major entrance for infectious pathogens and therefore mucosal immune responses serve as a first line of defence. Most current immunization procedures are obtained by parenteral injection and only few vaccines are administered by mucosal route, because of its low efficiency. However, targeting of mucosal compartments to induce protective immunity at both mucosal sites and systemic level represents a great challenge. Major efforts are made to develop new mucosal candidate vaccines by selecting appropriate antigens with high immunogenicity, designing new mucosal routes of administration and selecting immune-stimulatory adjuvant molecules. The aim of mucosal vaccines is to induce broad potent protective immunity by specific neutralizing antibodies at mucosal surfaces and by induction of cellular immunity. Moreover, an efficient mucosal vaccine would make immunization procedures easier and be better suited for mass administration. This review focuses on contemporary developments of mucosal vaccination approaches using different routes of administration.
黏膜表面是感染病原体的主要入口,因此黏膜免疫反应是第一道防线。大多数当前的免疫程序是通过注射给药获得的,只有少数疫苗通过黏膜途径给药,因为其效率低。然而,通过靶向黏膜隔室在黏膜部位和全身水平诱导保护性免疫是一个巨大的挑战。人们正在努力通过选择具有高免疫原性的合适抗原、设计新的黏膜给药途径和选择免疫刺激性佐剂分子来开发新的黏膜候选疫苗。黏膜疫苗的目的是通过在黏膜表面诱导特异性中和抗体和诱导细胞免疫来诱导广泛有效的保护性免疫。此外,有效的黏膜疫苗将使免疫程序更容易,并更适合大规模管理。本综述重点介绍了使用不同给药途径的黏膜疫苗接种方法的最新进展。