Lee A
School of Microbiology and Immunology, University of New South Wales, Sydney, Australia.
J Gastroenterol. 1996 Nov;31 Suppl 9:69-74.
The initial steps have been taken towards the development of a vaccine against the human gastroduodenal pathogen, Helicobacter pylori. Proof of principle was achieved when mice were protected against challenge with living Helicobacter felis, a close relative of the human pathogen, following oral immunization with H. felis sonicate and the mucosal adjuvant, cholera toxin. Similar results with H. pylori antigen have allowed development of possible human vaccines. Recombinant urease protein has been proposed as a major vaccine candidate, together with the heat-labile toxin of Escherichia coli as the adjuvant. Probably the most significant finding in the early vaccine studies was that immunization of already infected mice resulted in a cure of Helicobacter infection. The possibility of a therapeutic vaccine makes commercial development more attractive, as large populations could be immunized without the potential for development of drug-resistant strains that currently restricts widespread antibiotic use. For advanced societies with powerful economies yet a high prevalence of H. pylori, such as Japan, vaccine development should become a high national health priority.
针对人类胃十二指肠病原体幽门螺杆菌的疫苗研发已迈出了初步步伐。在用猫幽门螺杆菌超声裂解物和黏膜佐剂霍乱毒素进行口服免疫后,小鼠受到了对其近亲——活的猫幽门螺杆菌攻击的保护,从而实现了原理验证。幽门螺杆菌抗原的类似结果使得可能的人类疫苗得以研发。重组脲酶蛋白已被提议作为主要的疫苗候选物,同时大肠杆菌不耐热毒素作为佐剂。早期疫苗研究中可能最重要的发现是,对已感染小鼠进行免疫会导致幽门螺杆菌感染的治愈。治疗性疫苗的可能性使商业开发更具吸引力,因为可以对大量人群进行免疫,而不会出现目前限制广泛使用抗生素的耐药菌株产生的可能性。对于像日本这样经济强大但幽门螺杆菌感染率很高的发达社会,疫苗研发应成为国家高度重视的卫生优先事项。