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Patients receiving a graft from a MUD, MMUD or MFD received short course MTX and CsA.
Thus, patients receiving a graft from a cadaveric donor might be at a higher risk of TB.
Only patients receiving a graft from a donor staying <4 days in an intensive care unit and not having an alcohol-induced accident were included in the study.
The ability of T-cell to inhibit the growth of mycobacteria was impaired more in patients receiving a graft from a cadaveric donor than in patients receiving a graft from a living relative donor, because more immunosuppressive agents must be administrated against acute cellular rejection.
Recipients receiving a graft from a cadaveric donor and the preoperative evidence of latent TB were two major risk factors for developing TB in liver or kidney transplant recipients.
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Some patients, however, develop a positive crossmatch to donor lymphocytes and cannot receive a graft from that donor.
Kidney transplant recipients who received a graft from a dopamine treated donor had a significantly decreased need for dialysis after kidney transplantation compared to the untreated control group.
Thirty patients had received a graft from a deceased donor (42.3%).
Forty-two patients (22 female, 10 male, aged 11-47 years) received a graft from a living related donor and 10 from a deceased donor.
Patients with acute promyelocytic leukemia and those who received a graft from a syngeneic, cord blood or haploidentical donor were excluded.
A total of 162 patients received a human leukocyte antigen (HLA -matched sibling transplant, 101 received a matcHLA -matchedd donor (MUD) transiblingand 26 received a graftransplanton-HLA-matched related donor.
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