|Title||Effects of sample timing and treatment on gene expression in early acute renal allograft rejection.|
|Publication Type||Journal Article|
|Year of Publication||2011|
|Authors||Günther, OP, Lin, D, Balshaw, RF, Ng, RT, Hollander, Z, Wilson-McManus, J, W McMaster, R, McManus, BM, Keown, PA|
|Corporate Authors||Biomarkers in Transplantation Team|
|Date Published||2011 Feb 15|
|Keywords||Adult, Aged, Apoptosis, Biopsy, Case-Control Studies, Cell Cycle, DNA Damage, Female, Gene Expression Profiling, Graft Rejection, Humans, Immunosuppressive Agents, Kidney, Kidney Transplantation, Male, Middle Aged, Signal Transduction, Time Factors, Transplantation, Homologous|
BACKGROUND: We have shown that genomic biomarkers in peripheral blood provide evidence of early graft rejection and may offer an important option for posttransplant monitoring, and we are working to improve this signature to maximize assay performance.
METHODS: This clinical refinement study (n=79) used gene expression profiling in a case-control design to compare whole blood samples between normal subjects (n=20) and patients with (n=20) or without (n=39) biopsy-confirmed acute rejection (BCAR).
RESULTS: Gene expression in peripheral blood from subjects with BCAR before treatment differed significantly from that of normal subjects and transplant recipients without BCAR. Hierarchical clustering and principal component analysis showed that samples obtained 1 to 5 days after the start of treatment of BCAR were segregated across both groups before treatment or without BCAR and that this was closely related to the time lag between treatment and sampling. Genes differentially expressed during BCAR included FKSG49, LMAN2, NFYC, LIMK2, JUNB, NASP, MALAT1, ITGAX, HLA-J, FKBP1A, and RBMS1, and gene ontology analysis highlighted changes in networks related to cytoskeletal reorganization, apoptosis, and immune signaling, whereas after treatment change highlighted pathways of cellular metabolism, cell-cycle regulation, DNA damage, and apoptosis.
CONCLUSION: Gene expression in the peripheral blood is associated with BCAR, and the pattern of expression changes rapidly after treatment. This may offer a potential tool for diagnosis of rejection and immunologic monitoring of response to treatment, which is now being evaluated in a large multicenter international study.