Drug Delivery Research Laboratory, Department of Pharmaceutical Sciences, Dr. Harisingh Gour Vishwavidyalaya, Sagar, Madhya Pradesh, 470003, India.
Curr Infect Dis Rep. 2011 Feb;13(1):4-12. doi: 10.1007/s11908-010-0152-x.
Hepatitis B is a necroinflammatory liver disease manifested with subacute to acute symptoms, liver cirrhosis, and mortality. Parenteral alum-adsorbed hepatitis B surface antigenic (HBsAg) vaccination, although available, poses serious concerns regarding inability to induce both cell-mediated and mucosal immune response. In this context, oral delivery may be a prospective solution to the issues associated with conventional vaccination. However, the strategy is detrimental to the antigenic substances, suffers various physical/chemical barriers, and impedes poor transcytosis via mucosal route. Therefore, surface-engineered novel carrier-based approaches are reportedly promising for effective HBsAg oral vaccine delivery. This review focuses on the efforts for developing oral mucosal vaccine against hepatitis B, with considerable attention on novel drug delivery systems for spatial distribution of antigenic substance to the immune effector cells and organs.
乙型肝炎是一种坏死性炎症性肝病,表现为亚急性至急性症状、肝硬化和死亡率。虽然可获得的铝吸附乙型肝炎表面抗原(HBsAg)的注射用疫苗存在无法同时诱导细胞介导和黏膜免疫应答的严重问题。在这种情况下,口服给药可能是解决与传统疫苗相关问题的一种有前途的方法。然而,该策略不利于抗原物质,遭受各种物理/化学障碍,并阻碍通过黏膜途径的不良转胞吞作用。因此,据报道,表面工程化的新型基于载体的方法对于有效的 HBsAg 口服疫苗递送是有希望的。本综述重点介绍了开发乙型肝炎口服黏膜疫苗的努力,特别关注新型药物递送系统,以便将抗原物质空间分布到免疫效应细胞和器官。