DNA vaccines, with which the antigen is synthesized in vivo after direct in
troduction of its encoding sequences, offer a unique method of immunization
that may overcome many of the deficits of traditional antigen-based vaccin
es. By virtue of the sustained in vive antigen synthesis and the comprised
stimulatory CpG motifs, plasmid DNA vaccines appear to induce strong and lo
nglasting humoral (antibodies) and cell-mediated (T-help, other cytokine fu
nctions and cytotoxic T cells) immune responses without the risk of infecti
on and without boost. Other advantages over traditional antigen-containing
vaccines are their low cost, the relative ease with which they are manufact
ured, their heat stability, the possibility of obtaining multivalent vaccin
es and the rapid development of new vaccines in response to new strains of
pathogens. The antigen-encoding DNA may be in different forms and formulati
ons, and may be introduced into cells of the body by numerous methods. To d
ate, animal models have shown the possibility of producing effective prophy
lactic DNA vaccines against numerous viruses as well as other infectious pa
thogens. The strong cellular responses also open up the possibility of effe
ctive therapeutic DNA vaccines to treat chronic viral infections. (C) Elsev
ier, Paris.