The aim of this randomized prospective study in renal transplant recipients is to investigate immunological short and long-term effects of an IVIG induction therapy. Furthermore clinical endpoints (patient and graft survival, incidence of acute and chronic rejection, infectious diseases and graft function) up to three years posttransplant will be analyzed.
Intravenous immunoglobulin (IVIG) preparations are known to be effective in the treatment of various autoimmune and inflammatory disorders due to their immunomodulatory and antiinflammatory properties. It has been demonstrated that IVIG is effective in the treatment of acute vascular rejection and steroid resistant cellular rejection. Furthermore, IVIG has been used to inhibit production of lymphocytotoxic antibodies in highly sensitized patients so that successful cadaveric or living renal transplantation could be performed. The aim of this randomized prospective study in renal transplant recipients is to investigate immunological short and long-term effects of an IVIG induction therapy on Th1, Th2 and B-cell/monocyte responses, expression of adhesion molecules, costimulatory factors and cytokine receptors and on secretion of immunoregulatory autoantibodies (anti-F(ab)-, anti-F(ab')2G-, anti-hinge autoantibodies). These autoantibodies have been shown to significantly affect the risk of chronic rejection and graft loss. Furthermore, clinical endpoints (patient and gaft survival, incidence of acute and chronic rejection, infectious diseases and graft function) up to 3 years will be analyzed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Department of Internal Medicine, University of Giessen
Giessen, Germany
patient survival
Time frame: 1 year / 3 years / 5 years posttransplant
graft survival
Time frame: 1 year / 3 years / 5 years posttransplant
acute rejection
Time frame: 1 year
chronic allograft nephropathy
Time frame: 3 years / 5 years posttransplant
graft function
Time frame: 1 year / 3 years / 5 years
infectious complications
Time frame: 1 year
immunoglobulin levels
Time frame: 1 year
regulatory autoantibody levels
Time frame: 1 year / 3 years / 5 years
Th1 and Th2 responses
Time frame: 1 year / 3 years
B-cell/monocyte responses
Time frame: 1 year / 3 years
Expression of adhesion molecules, costimulatory molecules and cytokine receptors
Time frame: 1 year / 3 years
proteinuria (quantitative assessment)
Time frame: 1 year / 3 years
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