Department of Medical Biotechnology, School of Medicine, Fasa University of Medical Sciences, Fasa, Iran.
Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
Arch Microbiol. 2023 Jul 19;205(8):289. doi: 10.1007/s00203-023-03629-2.
Various infectious agents affect human health via the oral entrance. The majority of pathogens lack approved vaccines. Oral vaccination is a convenient, safe and cost-effective approach with the potential of provoking mucosal and systemic immunity and maintaining individual satisfaction. However, vaccines should overcome the intricate environment of the gastrointestinal tract (GIT). Oral protein-based antigen vaccines (OPAVs) are easier to administer than injectable vaccines and do not require trained healthcare professionals. Additionally, the risk of needle-related injuries, pain, and discomfort is eliminated. However, OPAVs stability at environmental and GIT conditions should be considered to enhance their stability and facilitate their transport and storage. These vaccines elicit the local immunity, protecting GIT, genital tract and respiratory epithelial surfaces, where numerous pathogens penetrate the body. OPAVs can also be manipulated (such as using specific incorporated ligand and receptors) to elicit targeted immune response. However, low bioavailability of OPAVs necessitates development of proper protein carriers and formulations to enhance their stability and efficacy. There are several strategies to improve their efficacy or protective effects, such as incorporation of adjuvants, enzyme inhibitors, mucoadhesive or penetrating devices and permeation enhancers. Hence, efficient delivery of OPAVs into GIT require proper delivery systems mainly including smart target systems, probiotics, muco-adhesive carriers, lipid- and plant-based delivery systems and nano- and microparticles.
各种感染性病原体通过口腔进入途径影响人类健康。大多数病原体缺乏已批准的疫苗。口服疫苗接种是一种方便、安全且具有成本效益的方法,具有激发黏膜和全身免疫以及保持个体满意度的潜力。然而,疫苗应该克服胃肠道(GIT)的复杂环境。口服蛋白型抗原疫苗(OPAVs)比注射疫苗更容易管理,并且不需要经过培训的医疗保健专业人员。此外,还消除了与针相关的伤害、疼痛和不适的风险。然而,应该考虑 OPAVs 在环境和 GIT 条件下的稳定性,以增强其稳定性并促进其运输和储存。这些疫苗引发局部免疫,保护胃肠道、生殖道和呼吸道上皮表面,其中许多病原体穿透身体。OPAVs 还可以被操纵(例如使用特定的结合配体和受体)以引发靶向免疫反应。然而,OPAVs 的生物利用度低,需要开发适当的蛋白质载体和制剂来增强其稳定性和功效。有几种策略可以提高它们的功效或保护作用,例如加入佐剂、酶抑制剂、黏膜黏附或穿透装置以及渗透增强剂。因此,将 OPAVs 有效递送到 GIT 需要适当的递送系统,主要包括智能靶向系统、益生菌、黏膜黏附载体、脂质和植物来源的递送系统以及纳米和微粒。