Transplantation of insulin-secreting tissue represents a physiologic approa
ch to reverse diabetes mellitus. Pancreas transplants yield a remarkable en
hancement in quality of life and appear to modify the devastating neurovasc
ular complications of diabetes. A more attractive approach is transplantati
on of insulin-secreting cells,a procedure of low invasiveness with the exci
ting prospect of modulating graft immunogenicity be fore transplantation, s
o as to minimize requirements for toxic immunosuppressive drugs. The Surgic
al-Medical Research Institute at the University of Alberta in Edmonton, and
several others centres throughout the world, has demonstrated that islet c
ell transplants can reverse insulin dependence and induce remarkable glycem
ic stability for several years. However, widespread success has been denied
because of insufficient donor tissue, early failures to reverse insulin de
pendence and the loss of graft function with time. Promising new research a
pproaches to these problems are reviewed, including xenogeneic sources of c
ells, engineering islet cells with genes that induce expression of immunopr
otective molecules, and neogenesis factors that may sustain populations of
transplanted beta cells.