What is the significance of having O- blood type with antigens C-, c+, Co(a)+, Co(b)-, Cw-, Di(a)-, Di(b)+, Do(a)+, Do(b)+, E-, e+, Fy(a)+, Fy(b)+, Hr(b), Hr(s)+, Hy+, Jk(a)+, Jk(b)+, Jo(a)+, Js(a)-, Js(b)+, K-, k+, Kp(a)-, Kp(b)+, Lu(a)-, Lu(b)+, M-, Mi(a)-, N+, S-, s+, U+, V-, Vs-, Yt(a)+, Yt(b)- in the context of living kidney donation?

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Blood Type O- with Multiple Antigens in Living Kidney Donation: Compatibility Assessment

For a living kidney donor with O- blood type and the specified antigen profile, comprehensive HLA typing and crossmatching are essential to determine compatibility with the intended recipient and minimize rejection risk.

ABO Blood Type Significance

The O- blood type is particularly valuable in living kidney donation because:

  • Type O donors are universal donors for ABO compatibility, able to donate to recipients with any blood type (O, A, B, or AB) 1
  • The negative Rh factor (O-) further increases compatibility options
  • ABO compatibility is the first critical step in determining donor-recipient matching 1

HLA Antigen Significance

The extensive antigen profile provided indicates a detailed HLA typing that includes:

  • Class I antigens: A, B, C (including C-, c+)
  • Class II antigens: DP, DQ, DR (including E-, e+)
  • Minor blood group antigens: Duffy (Fy), Kidd (Jk), Kell (K, k), etc.

Key Compatibility Considerations:

  1. HLA Matching Priority:

    • HLA-DR and HLA-DQ matching are particularly important for graft survival 1
    • Mismatches in HLA-DQ antigens correlate with higher risk of donor-specific antibody (DSA) development and rejection 1
  2. Crossmatching Requirements:

    • Flow cytometry or anti-human globulin enhanced complement-dependent cytotoxicity (AHG-CDC) crossmatching is mandatory 1
    • Both T-cell and B-cell crossmatches must be negative to proceed with transplantation 1
    • Historical, current, and pretransplant sera must all be tested against donor cells 1
  3. Antibody Assessment:

    • The recipient must be tested for preformed antibodies against the donor's HLA antigens 1
    • Panel reactive antibody (PRA) testing helps determine the degree of sensitization 1

Clinical Implications

  1. Rejection Risk Assessment:

    • The extensive antigen profile allows for precise matching with potential recipients
    • Eplet mismatches (specific amino acid sequences within HLA molecules) may better predict rejection risk than broad antigen matching 2
    • Recipients with ≥20 eplet mismatches have 2.16 times higher risk of acute rejection 2
  2. Paired Donation Consideration:

    • If direct donation is not possible due to incompatibility, kidney paired donation should be considered 1
    • O- donors are particularly valuable in paired donation chains due to their universal donor status
  3. Post-Transplant Management:

    • Blood transfusions post-transplant must consider both donor and recipient blood types 3
    • For ABO-incompatible transplants, special immunosuppression protocols are required 1

Practical Approach to Compatibility Assessment

  1. Initial Screening:

    • Confirm ABO compatibility between donor and recipient
    • Perform HLA typing for Class I (A, B, C) and Class II (DP, DQ, DR) 1
  2. Detailed Compatibility Testing:

    • Perform crossmatching using both flow cytometry and AHG-CDC methods 1
    • Test for donor-specific antibodies in the recipient 1
    • Calculate eplet mismatch load for more precise immunological risk assessment 2
  3. Risk Stratification:

    • Low risk: 0-2 HLA mismatches, negative crossmatch, no DSA
    • Moderate risk: 3-4 HLA mismatches, negative crossmatch, no DSA
    • High risk: 5-6 HLA mismatches, history of sensitization, or presence of DSA 4

Pitfalls to Avoid

  • Don't rely solely on broad antigen matching: Eplet mismatches may better predict rejection risk, especially in recipients considered low immunological risk (0-2 broad antigen mismatches) 2
  • Don't ignore historical sensitization: Previous pregnancies, transfusions, or transplants can increase rejection risk 5
  • Don't overlook the importance of HLA-DQ matching: Recent evidence suggests HLA-DQ matching significantly impacts long-term outcomes 1

By thoroughly evaluating this detailed antigen profile, transplant teams can optimize donor-recipient matching, minimize rejection risk, and maximize graft survival in living kidney donation.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Blood Transfusion Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Alloimmune Risk Stratification for Kidney Transplant Rejection.

Transplant international : official journal of the European Society for Organ Transplantation, 2022

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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