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Transpl Int. 2015 Oct;28(10):1205-15. doi: 10.1111/tri.12621. Epub 2015 Jul 6.

Difference in outcomes after antibody-mediated rejection between abo-incompatible and positive cross-match transplantations.

Author information

1
Department of Transplantation, Guy's and St Thomas' NHS Foundation Trust, London, UK.
2
Medical Research Council Centre for Transplantation, King's College London, London, UK.
3
Department of Histopathology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
4
Clinical Transplant Laboratory, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Abstract

Graft survival seems to be worse in positive cross-match (HLAi) than in ABO-incompatible (ABOi) transplantation. However, it is not entirely clear why these differences exist. Sixty-nine ABOi, 27 HLAi and 10 combined ABOi+HLAi patients were included in this retrospective study, to determine whether the frequency, severity and the outcome of active antibody-mediated rejection (AMR) were different. Five-year death-censored graft survival was better in ABOi than in HLAi and ABOi+HLAi patients (99%, 69% and 64%, respectively, P = 0.0002). Features of AMR were found in 38%, 95% and 100% of ABOi, HLAi and ABOi+HLAi patients that had a biopsy, respectively (P = 0.0001 and P = 0.001). After active AMR, a declining eGFR and graft loss were observed more frequently in HLAi and HLAi+ABOi than in ABOi patients. The poorer prognosis after AMR in HLAi and ABOi+HLAi transplantations was not explained by a higher severity of histological lesions or by a less aggressive treatment. In conclusion, ABOi transplantation offers better results than HLAi transplantation, partly because AMR occurs less frequently but also because outcome after AMR is distinctly better. HLAi and combined ABOi+HLAi transplantations appear to have the same outcome, suggesting there is no synergistic effect between anti-A/B and anti-HLA antibodies.

KEYWORDS:

ABO-incompatible; antibody-mediated rejection; donor-specific antibodies; kidney transplantation; positive cross-match

PMID:
26095452
DOI:
10.1111/tri.12621
[Indexed for MEDLINE]
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