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Updated: Mar 21, 2026

Mouse Kidney Transplantation: Models of Allograft Rejection
Published on: October 11, 2014
Borderline rejection in ABO-incompatible kidney transplantation.
Anna Sánchez-Escuredo1, Federico Oppenheimer1, Manel Solé2
1Nephrology and Renal Transplant Department, Hospital Clinic, Universitat de Barcelona, Barcelona, Spain.
Kidney transplant outcomes are similar for ABO-incompatible and ABO-compatible recipients. While ABO-incompatible transplants show more borderline rejection lesions on protocol biopsies, they do not have worse long-term histologic outcomes.
Area of Science:
- Nephrology
- Transplant Surgery
- Immunology
Background:
- Clinical outcomes for ABO-incompatible (ABOi) and ABO-compatible (ABOc) kidney transplantation (KT) are comparable.
- Protocol kidney biopsies (PKB) in ABOi KT recipients often show C4d positivity without overt antibody-mediated rejection (ABMR), but histologic progression remains unclear.
Purpose of the Study:
- To evaluate histologic parameters in PKB at 12 months post-transplant.
- To compare clinical outcomes at 1 year between ABOi and ABOc kidney transplant recipients.
- To investigate the histologic progression in ABOi kidney transplants.
Main Methods:
- A prospective observational study was conducted from 2009 to 2013.
- 146 ABOc and 30 ABOi living-donor KT recipients underwent PKB and indication biopsies.
- ABOi recipients received a desensitization protocol including rituximab, plasma exchange/immunoadsorption, and immunoglobulins.
Main Results:
- At 1 year, PKB revealed significantly more borderline rejection lesions in the ABOi group (23.3%) compared to the ABOc group (6.8%).
- C4d positivity was more frequent in the ABOi group (P=.001).
- No significant differences were observed in T-cell-mediated rejection, ABMR, interstitial fibrosis and tubular atrophy (IFTA), or transplant glomerulopathy between the groups at 1 year.
Conclusions:
- Protocol kidney biopsies at 1 year in ABOi kidney transplant recipients show an increased incidence of borderline lesions, irrespective of ABO titers, HLA incompatibility, or donor-specific antibodies.
- These borderline lesions do not correlate with increased rates of IFTA or transplant glomerulopathy.
- No significant clinical differences in outcomes were observed between ABOi and ABOc kidney transplant recipients at 1 year.
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