DNA vaccines represent one of the most significant developments in vac
cine technology in recent years. Although, in general, studies have pr
imarily focused on the induction of protective immune responses agains
t infectious pathogens, the technology may prove useful for other immu
ne-related diseases, including autoimmunity. Autoimmune disease result
s from a breakdown in tolerance to self antigens; however, the same fu
ndamental immunological reactions that control immune responses to for
eign antigens are also likely to operate during the course of autoimmu
ne disease. These include the reciprocal regulation of Th cell subsets
, Th1 cells appear to be involved in many organ-specific autoimmune di
seases while suppression of disease is associated with cells of the Th
2 phenotype. It has been possible, therefore, to suppress many of the
pathological consequences of autoimmunity by manipulating the Th1/Th2
cell balance, The induction of Th2 responses by DNA immunization might
therefore be expected to have a profound effect on the course of auto
immune disease. Indeed, we have demonstrated that DNA immunization can
protect animals against the autoimmune central nervous system inflamm
atory disease, experimental autoimmune encephalomyelitis (EAE). As man
y other autoantigens have now been identified, the application of this
technology to other autoimmune diseases warrants investigation.