Table 1.
Protocol Induction |
Maintenance | n | Reported adverse events | Reference | |
---|---|---|---|---|---|
ATG (basiliximab for 2nd Tx) + belatacept | Sirolimus ± MMF | 5 | (Both belatacept and efalizumab group) | Oral ulcer (many), nausea (3), diarrhea (4), neutropenia (3), thrombocytepenia (1),Rash or erythema (2) | 6, 7 |
ATG (basiliximab for 2nd Tx) + efalizumab | Sirolimus ± MMF | 5 | (Efalizuma b group) | Rash/Erythema (2), partial portal vein thrombosis (1) | |
ATG + etanercept | Cyclosporine + everolimus or MMF | 6 | Oral ulcer (6), leukopenia (6), transient elevations of liver enzymes (6), acute cholecystitis (2), increased serum creatinine (6), >25% decreased GFR (2), hypertension (1), hyperlipidemia (1) | 4 | |
ATG + daclizumab + etanercept | MMF + sirolimus ± low-dose tacrolimus | 8 | Lymphopenia (5), transient neutropenia (5), oral ulcer (8) | 61 | |
Alemtuzumab + etanercept | Sirolimus + tacrolimus/MMF | 3 | Leukopenia (3), lymphopenia (3), Skin rash (3) | 5 | |
Daclitumab ± infliximab, | Sirolimus + tacrolimus | 16 | Aspication pneumonia (1), parvovirus infection (1), HES (1), short-term memory loss 1), renal dysfunction (1), exzema (1) and insomnnia/depression (1), Leukopenia/neutropenia (9), serum creatinine elevation (2), macroalbuminuria (5), mild hypertension (1), hyperlipidemia (14), mouth ulcer, peripheral edema, insomnia, tremor, anxiety, headache, gynecological abnormalities, bone marrow suppression, electrolyte abnormalities, proteinuria | 62 | |
Daclitumab + etanercept + exenatide | Sirolimus + tacrolimus | 6 | Weight loss (6), nausea (6), vomitting (6), viral stomatitis (1), severe anemia (1), elevated creatinine (2), myonecrosis (1) | 63 | |
Daclitumab + Efalizumab | MMF + tacrolimus | 4 | Anemia (2), elevation of liver enzymes (2), | 8 |
The numbers in parentheses indicate number of patients with individual AE.