Reversibility from delayed hyperacute rejection in ABO-incompatible renal transplantation: histopathological findings of renal allograft biopsy
- PMID: 15848507
- DOI: 10.1016/j.transproceed.2004.12.044
Reversibility from delayed hyperacute rejection in ABO-incompatible renal transplantation: histopathological findings of renal allograft biopsy
Abstract
ABO-incompatible renal transplantation (ABOIRTx) tend to lead to blood type antibody-mediated rejection, the so-called delayed hyperacute rejection (DHAR), which results in short-term graft loss. To clarify the accurate incidence and prognostic value of DHAR among ABOIRTx, we reviewed biopsy specimens obtained from ABOKTx allografts with abrupt dysfunction during the early period after transplantation. Among 74 ABOIRTx patients, 34 patients displayed allograft dysfunction within 14 days following transplantation. The biopsy specimens were classified based on the Banff schema. The pathological diagnosis of ABO blood type antibody-mediated humoral rejection (ABO-AMHR) was made by the following 3 findings: Specimens with all of above-mentioned findings were categorized as severe ABO-AMHR; those with at least one findings, were categorized as mild ABO-AMHR. All patients were treated with steroid pulse therapy and/or modification of other immunosuppressants. Group 1 consisted of severe ABO-AMHR (n = 6); group 2 consisted of mild ABO-AMHR (n = 5); group 3 consisted of acute cellular rejection (n = 3); group 4 consisted of recovery phase of ATN (n = 11); group 5 consisted of calcineurin inhibitor toxicity (n = 2); and group 6 consisted of normal histology (n = 5). One of 6 patients (16%) in group 1 lost the graft because of DHAR irreversible by antirejection and anticoagulation therapy. However, there has been no clear definition of histpathological criteria for DHAR after ABO-incompatible kidney transplantation. The definition must prognosticate whether the rejection process is reversible.
Similar articles
-
ABO-incompatible live donor renal transplantation using blood group A/B carbohydrate antigen immunoadsorption and anti-CD20 antibody treatment.Xenotransplantation. 2006 Mar;13(2):148-53. doi: 10.1111/j.1399-3089.2006.00280.x. Xenotransplantation. 2006. PMID: 16623810
-
Peritubular capillary deposition of C4d complement fragment in ABO-incompatible renal transplantation with humoral rejection.Clin Transplant. 1999;13 Suppl 1:33-7. Clin Transplant. 1999. PMID: 10751054
-
Acute humoral rejection and C4d immunostaining in ABO blood type-incompatible liver transplantation.Liver Transpl. 2006 Mar;12(3):457-64. doi: 10.1002/lt.20652. Liver Transpl. 2006. PMID: 16498648
-
Xenotransplantation and ABO incompatible transplantation: the similarities they share.Transfus Apher Sci. 2006 Aug;35(1):45-58. doi: 10.1016/j.transci.2006.05.007. Epub 2006 Aug 14. Transfus Apher Sci. 2006. PMID: 16905361 Review.
-
Current status of ABO-incompatible kidney transplantation in children.Pediatr Transplant. 2005 Apr;9(2):148-54. doi: 10.1111/j.1399-3046.2004.00234.x. Pediatr Transplant. 2005. PMID: 15787785 Review.
Cited by
-
Non-Invasive Biomarkers for Early Diagnosis of Kidney Allograft Dysfunction: Current and Future Applications in the Era of Precision Medicine.Medicina (Kaunas). 2025 Feb 4;61(2):262. doi: 10.3390/medicina61020262. Medicina (Kaunas). 2025. PMID: 40005378 Free PMC article. Review.
-
Protocol Biopsies in Kidney Transplant Recipients: Current Practice After Much Discussion.Biomedicines. 2025 Jul 7;13(7):1660. doi: 10.3390/biomedicines13071660. Biomedicines. 2025. PMID: 40722731 Free PMC article. Review.
-
Highly individual- and tissue-specific expression of glycoprotein group A and B blood antigens in the human kidney and liver.BMC Immunol. 2021 Oct 1;22(1):66. doi: 10.1186/s12865-021-00456-2. BMC Immunol. 2021. PMID: 34598667 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical