Diabetes type 1A is an autoimmune condition characterized by lymphocytic in
filtration of islets and selective destruction of insulin-secreting beta-ce
lls. Numerous investigators have prevented diabetes in animal models with a
variety oi antigens and routes of administration. It is also now possible
to identify high-risk individuals even before the appearance of autoantibod
ies. These advances have created the opportunity to design and begin human
prevention trials. This review focuses on a variety of immunomodulatory app
roaches (including administration of adjuvants, autoantigens, T-cells, T-ce
ll receptors, and DNA) that ive have collectively termed immunologic "vacci
nation." In addition, we discuss the potential benefits and dangers of thes
e approaches and issues relating to the design of human trials.