In healthy persons insulin secreting beta-cells of the pancreas regulate bl
ood glucose levels within a narrow physiological range. Since the detection
of insulin in 1922 by Banting and Best, subcutaneous insulin replacement h
as remained the sole treatment modality for insulin-dependent diabetes mell
itus (IDDM). However, even trained patients undergoing intensive insulin th
erapy fail to achieve normal function of the pancreatic beta-cells. one app
roach to solve this problem is pancreas and islet cell transplantation. Bec
ause of technical problems, limited number of transplantable organs and tox
icity of immunosuppressive therapy, both are still in an experimental state
. An alternative approach is the development of genetically modified insuli
n secreting cell lines for replacement of islet cells. So far, experiments
support the expectation to develop genetically manipulated cell lines who i
mitate the function of islet beta-cells and are protected from the immune r
esponse. The ultimate goal is the development of an engineered human beta-c
ell line and, after animal experiments, to use it for treatment of patients
with IDDM.