Islet transplants after kidney transplants: a step toward insulin freedom?

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Type 1 diabetes mellitus. Documentation of negative basal and stimulated C-peptide (a basal level of \</= 0.2 ng/ml before IV administration of 1 mg of glucagon, and a glucagon stimulated C-peptide \</= 0.8 ng/ml) and diagnosis of diabetes for at least 5 years. * Recipient of renal transplant with good function (serum creatinine \</= 1.6 mg/dl, creatinine clearance \>/=60 ml/min and albumin excretion \</= 300 mg/24 hr) for \>3 months. * Stable immunosuppression consisting of any combination of sirolimus, tacrolimus, MMF or \</= 5 mg/day of corticosteroids for at least 3 months, without major complications. * No history of acute rejection episodes related to renal graft in last 12 months and low risk for developing acute rejection (first renal transplant, PRA \<25%, negative kidney crossmatch by B, T, flow cytometry) * Under the continuing care of a renal transplant nephrologist/surgeon. * No evidence of liver disease (liver enzymes \< twice the upper limit of normal for each of ALT and AST, bilirubin \< 2 mg/dl, albumin \> 3.5 g/dl, and PT and PTT \</= 1.1 x the upper limit of normal). * Ability to comply with post-transplant regimen, including immunosuppression, insulin pump therapy and metabolic testing. Patients will be required to perform self-monitoring of blood glucose a minimum of four times daily, and provide complete records of blood glucose levels and insulin doses. * Ability to give informed consent. * Age greater than or equal to 18 years or less than or equal to 65 years. * Subjects that have always been managed on a sirolimus/tacrolimus/MMF/low-dose corticosteroid (\</=5mg) immunosuppressive regimen and never required conversion must provide a signed letter from their transplant nephrologist /surgeon documenting this. * Subjects converted to a sirolimus/tacrolimus/MMF/low-dose corticosteroid immunosuppressive regimen, must provide proof of informed consent regarding immunosuppressive conversion in one of the following formats. * Subjects that converted to sirolimus/tacrolimus/MMF/low-dose corticosteroids (\</=5mg) due to best patient care (not to qualify for islet transplantation) must provide a signed letter from their transplant nephrologists/surgeon indicating the medical reason(s) for immunosuppression conversion (with the date indicated). * Subjects that converted to a sirolimus/tacrolimus/MMF/low-dose corticosteroid (\</=5mg) immunosuppressive regimen for the purpose of qualifying for islet transplantation must provide a signed immunosuppression conversion consent form. Exclusion Criteria: * Poor renal allograft function (serum creatinine \> 1.6 mg/dl, creatinine clearance \< 60ml/min, albumin excretion \>300 mg/24hr) * History of acute rejection related to renal graft in last 12 months or "high risk" for acute rejection (more than one previous renal transplant, PRA \>25%, positive kidney crossmatch by B, T, flow cytometry) * Current immunosuppression therapy with corticosteroids \>5mg/day. * Significant liver disease (including elevation of liver enzymes \> twice the upper limit of normal for each of ALT and AST, bilirubin \> 2 mg/dl, albumin \< 3.5 g/dl, liver masses including portal vein thrombosis, evidence of portal hypertension, or significant, untreated gallbladder disease (i.e., gallstones). * Significant cardiovascular disease, including non-correctable coronary artery disease with ejection fraction \< 50% and/or recent myocardial infarction (within last 12 months); extensive peripheral vascular disease not correctable by surgery or untreated proliferative retinopathy. * Recent unresolved acute infection, or chronic infection, including tuberculosis, HIV, HBV, HCV, CMV or positive skin test for TB. * Any history of malignancy, except squamous or basal skin cancer or in situ cancer of the cervix. * Recent history of non-compliance, or inability to demonstrate capacity to comply with strict blood glycemic control and insulin pump therapy. * Psychiatric illness that is untreated, or likely to interfere significantly with transplantation despite treatment. * Presence of preformed antibodies on panel reactive antibody screening \> 25%. * Body mass index (BMI) greater than 30. * Age less than 18 years or greater than 65 years. * Presence of a chronic disease that must be chronically treated with one or more of the following medications: glucocorticoids, diazoxide, bumetanide, haloperidol, chlorpromazine, desipramine, doxepin, imipramine, levodopa, morphine, L-asparaginase, cyclophosphamide, isoniazid, heparin, nalidixic acid, or any other agents that may adversely influence glycemic control and which may confound the interpretation of Graft Success post-transplant. * Pregnant women, women intending future pregnancy, women of reproductive potential who are unable or unwilling to follow effective contraceptive measures for the duration of immunosuppressive therapy, and women presently breast feeding are ineligible due to the unknown effects of these drugs on the fetus and nursing infant. * Active alcohol or substance abuse, including cigarette smoking (must be abstinent for \> 3 months). * Hyperlipidemia (total cholesterol \> 260 mg/dl, LDL \> 130 mg/dl, and/or triglycerides \> 300 mg/dl) despite appropriate treatment. * Anemia (Hgb \< 12 g/dl) or other hematologic disorders that require medical attention. * Increased risk of bleeding (platelet count \< 80,000; INR \> 1.5), other chronic hemostasis disorders, or treatment with chronic anticoagulant therapy (i.e., heparin or warfarin).