What is a safe antibody titre for an ABO (Abo blood group) incompatible kidney transplant?

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Last updated: May 13, 2025View editorial policy

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From the Guidelines

For ABO-incompatible (ABOI) kidney transplantation, a pre-transplant anti-blood group antibody titre of 1:8 or lower is generally considered safe for proceeding with transplantation. This threshold is based on clinical experience showing significantly higher rates of antibody-mediated rejection when transplants proceed with titres above 1:8 1. The desensitization protocol typically aims to reduce titres to this level or below before surgery.

Key Considerations

  • The protocol usually includes rituximab (375 mg/m² given 2-4 weeks pre-transplant), plasmapheresis or immunoadsorption sessions (typically 2-6 sessions depending on initial titre levels), and intravenous immunoglobulin (IVIG, often 0.1 g/kg after each plasmapheresis) 1.
  • Maintenance immunosuppression typically consists of tacrolimus, mycophenolate mofetil, and steroids, started 1-2 weeks before transplantation.
  • Post-transplant monitoring of antibody titres is essential, particularly in the first two weeks, with additional plasmapheresis performed if titres rise above 1:8.

Rationale

  • Some centers with extensive experience may accept titres up to 1:16 or 1:32, but this carries higher risk and requires more aggressive immunosuppression 1.
  • The presence and quantity of antibodies to HLA antigens can fluctuate with time, and patients may display an anamnestic (memory) immune response leading to accelerated rejection despite a negative pretransplant crossmatch with current or pretransplant sera 1.

Important Factors

  • Methods used to test for the presence of alloantibodies should be sensitive and identify clinically relevant IgG antibodies to HLA antigens 1.
  • Newer assays, such as enzyme-linked immunosorbent assay (ELISA) and Flow Bead, have been introduced to identify antibodies specific to HLA antigens 1.

From the Research

Safe Titre for ABOI Kidney Transplant

  • A decrease in the isoagglutinin titer <1:8 is usually required for ABO-incompatible (ABOi) transplantation 2
  • The presence of high predesensitization titers may condition future transplantation 2
  • Baseline isoagglutinin titer does not influence the prognosis of ABOi patients after desensitization 2
  • A higher number of apheresis sessions was observed in patients with titer >128, but this does not influence the number of days of hospital admission 2

Desensitization Protocols

  • Desensitization protocols for ABO-incompatible kidney transplantation often include plasmapheresis, rituximab, and immunosuppressive drugs 3, 4, 5
  • A low-dose rituximab regimen for ABOI KTX is acceptable for preventing acute antibody-mediated rejection with a low incidence of delayed adverse events 3
  • Antigen-specific immunoadsorption, rituximab, and a conventional triple-drug immunosuppressive protocol can be used without splenectomy 4
  • A preconditioning protocol consisting of rituximab infusions, splenectomy, plasmapheresis, and pharmacologic immunosuppression enabled ABO-incompatible renal transplantation in patients with high (> 1:512) anti-A/B antibody titer 5

Outcomes of ABO-Incompatible Kidney Transplantation

  • Recent reports document outcomes for ABO-incompatible kidney transplantation similar to the outcomes of standard transplantation 6
  • Desensitization of the recipient to remove the antibodies and to prevent their rebound after transplantation is a key strategy for overcoming ABO incompatibility 6
  • A tailored desensitization approach can be the most efficient strategy, avoiding excess immunosuppression and related side effects 6

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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