Objective: Anti-thymocyte globulin-Fresenius is used for induction treatment in kidney transplantation. The antibody of rabbit originated against human leukocyte antigen A3 were demonstrated in the serum of patients who used antithymocyte globulin-Fresenius. We investigated whether anti-human leukocyte antigen A3 antibodies detected due to anti-thymocyte globulin administration had any efect on patient and allograf survival in short- and long-term follow-up.
Methods: Fify-one patients who underwent kidney transplantation between 2004 and 2014 were included in the study. Twenty-nine patients who underwent transplantation from deceased donors received an induction therapy consisting of anti-thymocyte globulin-Fresenius. Antibodies against the human leukocyte antigen were identified using the LABScreen panel reactive antibody class I/II kits with the Luminex method. The graf function and loss, patient survival, and the presence of acute/chronic rejection were investigated.
Results: Anti-human leukocyte antigen A3 antibody was detected in 41.3% of the patients receiving anti-thymocyte globulin induction (P = .001). This antibody disappeared at 234.4 days posttransplant. No diference was found regarding pretransplant and posttransplant sensitization of the patients who had posttransplant anti-human leukocyte antigen A3 positivity. The anti-thymocyte globulin dose and administration period were similar for anti-human leukocyte antigen A3 antibodypositive and -negative patients (P >.05). There was no significant diference between groups in short-term, first year, and long-term results of serum creatinine, estimated glomerular filtration rate, and proteinuria values (P >.05).
Conclusion: We demonstrated that xenogeneic anti-human leukocyte antigen A3 antibody could be detected in posttransplant serum of patients receiving anti-thymocyte globulin induction independent of the dose and duration. The development of this antibody was independent of the exposure of the patient to pre- and posttransplant sensitizing event or the presence of human leukocyte antigen A3 in the allograf. While this study did not demonstrate the efect of xenogeneic anti-human leukocyte antigen A3 antibody on graf and patient survival, retrospective multicenter cohort studies are needed on this issue.
Cite this article as: Usta Akgul S, Temurhan S, Kekik Cınar C, et al. Do xenogeneic anti-HLA-A3 antibody cause antibody-mediated rejection in kidney transplant? Turk J Nephrol. 2024;33(1):102-109.