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Background: Acute rejection occurs at any time following renal transplantation. The study aims to find the incidence, risk factors, and outcome of acute rejection in kidney transplantation. Materials and Methods: Retrospective cohort study conducted from January 2015 to April 2023, included patients with biopsy-proven acute graft rejection. Data were collected from electronic medical records. Rejection and no rejection groups were compared for the variables. Results: Out of 371 patients, acute rejection occurred in 36 (9.7%) patients at 1 year of transplantation. Thirty (8%) were early acute rejections (EARs) and 22 (6%) were late acute rejections (LARs). Higher human leukocyte antigen (HLA) mismatches, historical positive crossmatch, and history of blood transfusions were risk factors for acute rejection (P < 0.05). Incidence of LAR beyond 1 year was 11/23 (48%) in those who had received induction therapy at transplantation versus 5/29 (17.2%) in those who did not (P = 0.045). One out of five patients (3.4%) who received antithymocyte globulin (ATG) experienced EAR, in contrast to 8/18 (5.2%) patients who received basiliximab (P = 0.037). A complete response to treatment was observed in 22/30 (73.3%) patients with EAR and 2/22 (9.09%) with LAR (P < 0.001). At 23.77 ± 24.6 months of follow-up, graft survival was 12/12 (100%) in those with early T-cell-mediated rejection (TCMR) compared to 5/9 (55.6%) with late acute TCMR (P = 0.01). Conclusion: The incidence of acute rejection was highest within the first posttransplant year. Higher HLA mismatches, historical positive crossmatch, and history of blood transfusion were risk factors for acute rejection. ATG was effective in preventing EAR. LAR occurring beyond the first posttransplant year was independent of induction therapy at time of transplantation. Treatment response was better with EAR compared to LAR. Graft survival was better with early acute TCMR compared to late acute TCMR.

Background: Acute rejection occurs at any time following renal transplantation. The study aims to find the incidence, risk factors, and outcome of acute rejection in kidney transplantation. Materials and Methods: Retrospective cohort study conducted from January 2015 to April 2023, included patients with biopsy-proven acute graft rejection. Data were collected from electronic medical records. Rejection and no rejection groups were compared for the variables. Results: Out of 371 patients, acute rejection occurred in 36 (9.7%) patients at 1 year of transplantation. Thirty (8%) were early acute rejections (EARs) and 22 (6%) were late acute rejections (LARs). Higher human leukocyte antigen (HLA) mismatches, historical positive crossmatch, and history of blood transfusions were risk factors for acute rejection (P < 0.05). Incidence of LAR beyond 1 year was 11/23 (48%) in those who had received induction therapy at transplantation versus 5/29 (17.2%) in those who did not (P = 0.045). One out of five patients (3.4%) who received antithymocyte globulin (ATG) experienced EAR, in contrast to 8/18 (5.2%) patients who received basiliximab (P = 0.037). A complete response to treatment was observed in 22/30 (73.3%) patients with EAR and 2/22 (9.09%) with LAR (P < 0.001). At 23.77 ± 24.6 months of follow-up, graft survival was 12/12 (100%) in those with early T-cell-mediated rejection (TCMR) compared to 5/9 (55.6%) with late acute TCMR (P = 0.01). Conclusion: The incidence of acute rejection was highest within the first posttransplant year. Higher HLA mismatches, historical positive crossmatch, and history of blood transfusion were risk factors for acute rejection. ATG was effective in preventing EAR. LAR occurring beyond the first posttransplant year was independent of induction therapy at time of transplantation. Treatment response was better with EAR compared to LAR. Graft survival was better with early acute TCMR compared to late acute TCMR. [ABSTRACT FROM AUTHOR]

Background: Liver biopsy plays a crucial role in evaluating allograft dysfunction. Comprehensive analysis of the histological spectrum of complications, particularly rejection, in different time zones is lacking. Aim: To evaluate the histological spectrum of rejection, in four time zones, in a large Living donor liver transplant series. Patients and Methods: Retrospective analysis of 313 biopsies for the last 10 years of living donor liver transplantation (LDLT) recipients. 123 of which had rejection as diagnosis, were redistributed in four time zones [1-early ( 12) months] and were assessed for sixteen histological parameters. Results: Biopsies in time zone 1 (26.5%), 2 (20.7%), 3 (24.6%), and 4 (28.1%)] were nearly equal. Multiple coexistent complications existed in 12% of the cases. Rejection diagnosed in time zone groups: 1 = 22 (17.9%), 2 = 27 (22%), 3 = 36 (29.3%), and 4 = 38 (30.9%). Portal inflammation mixed type (P < 0.000), portal vein (P = 0.001) and hepatic vein endothelialitis (P < 0.000), portal eosinophils (P = 0.001), and lymphocytic bile duct damage (P = 0.01) were most pronounced in group 1. Perivenulitis without hepatic vein endothelialitis was observed (P = 0.03) in groups 3, whereas bile duct atypia (P = 0.01) and duct loss (P < 0.000) were observed in group 4. Multiple episodes of rejection displayed significant association with central perivenulitis (P = 0.002) and bile duct loss (P < 0.001). Conclusions: Histological analysis in large series of LDLT recipients highlights the spectrum of complications in different time zones. Late acute and chronic rejection occurred as early as 3 months posttransplant. Central perivenulitis and bile duct atrophy were associated with repeated episodes of rejection and deterioration.