The aim of this study is to evaluate whether anti-HLA donor-specific antibodies monitoring can be used as an effective tool for stratification of immunological risk in Polish kidney transplant recipients.
Monitoring of immune response is one of the most important goals in the management of the patients after kidney transplantation. Researchers and clinicians are trying to extend the survival of the renal graft. Currently, it is believed that the main cause of late transplant loss is antibody-mediated rejection (ABMR). Anti-HLA donor-specific antibodies (DSA) are a proven risk factor for the development of humoral rejection and transplant loss. Antibodies in sensitized recipients occur before transplantation (preformed) or may develop de novo (in 13% -30% of patients). DSA damage the graft in various mechanisms (complement activation, direct influence on endothelial cells, antibody-dependent cytotoxicity) leading to different clinical-morphological phenotypes. The pathogenicity of DSA is determined by number of their additional characteristics, such as: class, specificity, strength, C1q complement binding, IgG subclass . Monitoring the presence of DSA in the kidney recipient serum with the determination of their characteristics may improve the stratification of the risk of immunological loss of the renal allograft. There is no effective treatment for ABMR, hence DSA monitoring allows for early intervention such as biopsy or modification of immunosuppressive therapy at an early stage of rejection.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
100
Monitoring anti-HLA donor-specific antibodies in the patients serum at the time of kidney transplantation and 3, 12 and 24 months after the procedure. Blood samples from patients will be collected.
Department of Transplantation Medicine, Nephrology and Internal Medicine
Warsaw, Poland
Presence of anti-HLA donor-specific antibodies.
Binary variable (positive/negative).
Time frame: 24 months
Mean fluorescence intensity (MFI) of anti-HLA DSA.
Assessed when anti-HLA DSA positive. Mean fluorescence intensity (MFI) of anti-HLA DSA. \[units\]
Time frame: 24 months
Presence of C1q complement binding anti-HLA DSA.
Assessed when anti-HLA DSA positive. Binary variable (positive/negative).
Time frame: 24 months
Presence of IgG1 subclass of anti-HLA DSA.
Assessed when anti-HLA DSA positive. Binary variable (positive/negative).
Time frame: 24 months
Presence of IgG2 subclass of anti-HLA DSA.
Assessed when anti-HLA DSA positive. Binary variable (positive/negative).
Time frame: 24 months
Presence of IgG3 subclass of anti-HLA DSA.
Assessed when anti-HLA DSA positive. Binary variable (positive/negative).
Time frame: 24 months
Presence of IgG4 subclass of anti-HLA DSA.
Assessed when anti-HLA DSA positive. Binary variable (positive/negative).
Time frame: 24 months
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