Mestecky Jiri, Nguyen Huan, Czerkinsky Cecil, Kiyono Hiroshi
Department of Microbiology and Medicine, The University of Alabama at Birmingham, AL 35294-2170, USA.
Curr Opin Gastroenterol. 2008 Nov;24(6):713-9. doi: 10.1097/MOG.0b013e32830d58be.
Oral immunization with vaccines against intestinal infectious diseases has been extensively explored for several decades. Despite the immunologic and economic rationale behind oral immunization, only a few mucosal vaccines are available for the prevention of mucosal infections. Here, we summarize the current status of such vaccines, with a focus on intestinal infectious diseases, describe alternative approaches, and analyze advantages and difficulties encountered with a broad implementation of these vaccines.
Due to the limited absorption from the intestinal tract and sensitivity to degradation, oral vaccines composed of killed bacteria and viruses or antigens isolated from infectious agents have not been successful. New, live-attenuated bacterial and viral or edible plant-derived vaccines, however, have been recently introduced for this purpose. Furthermore, systemic immunization with vaccines composed of bacterial polysaccharides chemically coupled to suitable protein carriers induces high levels of IgG antibodies, which may provide immunity toward Salmonella typhi, Shigella, and Escherichia coli.
Further improvements in antigen-delivery systems, the development of adjuvants that are safe for mucosal application in humans, use of live-attenuated vaccines and microbial vectors, and production of certain vaccines in plant expression systems are likely to contribute to the broader use of oral vaccines in the future.
几十年来,人们一直在广泛探索通过口服疫苗来预防肠道传染病。尽管口服免疫背后有免疫学和经济学依据,但目前仅有少数黏膜疫苗可用于预防黏膜感染。在此,我们总结此类疫苗的现状,重点关注肠道传染病,描述替代方法,并分析广泛应用这些疫苗所遇到的优势和困难。
由于从肠道的吸收有限以及对降解敏感,由灭活细菌、病毒或从感染因子中分离的抗原组成的口服疫苗并未取得成功。然而,最近为此目的引入了新型的减毒活细菌和病毒疫苗或可食用植物源疫苗。此外,用化学偶联到合适蛋白质载体上的细菌多糖组成的疫苗进行全身免疫可诱导高水平的IgG抗体,这可能对伤寒沙门菌、志贺菌和大肠杆菌提供免疫力。
抗原递送系统的进一步改进、开发对人体黏膜应用安全的佐剂、使用减毒活疫苗和微生物载体以及在植物表达系统中生产某些疫苗,可能有助于未来更广泛地使用口服疫苗。