In animals, oral immunization can prevent or cure Helicobacter pylori infec
tion, and prevent reinfection. Several antigens of the pathogen have been i
dentified as protective antigens, and some appear to be well suited for use
in an human vaccine. Initial clinical studies have shown that urease is sa
fe in humans, and immunogenic in Helicobacter pylori-infected volunteers. T
he design of a protective vaccine in humans will probably depend upon the c
ombination of two or more antigens, the identification of the optimal route
of immunization, and the use of appropriate vaccine delivery systems. Beca
use a vaccine against Helicobacter pylori is likely to be effective regardl
ess of the mode of transmission of the infection, it represents a potential
alternative to current therapies, with the added advantage of having a dir
ect impact on the reservoir of the infection.