Publication

ABO-adjusted calculated panel reactive antibody (cPRA): A unified metric for immunologic compatibility in kidney transplantation

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Last modified
  • 06/25/2025
Type of Material
Authors
    Loren Gragert, Tulane UniversityMatthew Kadatz, Vancouver Coastal Health Research InstituteJames Alcorn, United Network for Organ Sharing, Richmond Virginia, USADarren Stewart, United Network for Organ Sharing, Richmond Virginia, USADoris Chang, Providence Hlth Res InstJagbir Gill, University of British ColumbiaRobert Liwski, Dalhousie UniversityHoward Gebel, Emory UniversityJohn Gill, University of British ColumbiaJames H Lan, Vancouver Coastal Health Research Institute
Language
  • English
Date
  • 2022-12-01
Publisher
  • WILEY
Publication Version
Copyright Statement
  • © 2022 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons.
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Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 22
Issue
  • 12
Start Page
  • 3093
End Page
  • 3100
Supplemental Material (URL)
Abstract
  • Implementation of the kidney allocation system in 2014 greatly reduced access disparity due to human leukocyte antigen (HLA) sensitization. To address persistent disparity related to candidate ABO blood groups, herein we propose a novel metric termed “ABO-adjusted cPRA,” which simultaneously considers the impact of candidate HLA and ABO sensitization on the same scale. An ethnic-weighted ABO-adjusted cPRA value was computed for 190 467 candidates on the kidney waitlist by combining candidate's conventional HLA cPRA with the remaining fraction of HLA-compatible donors that are ABO-incompatible. Consideration of ABO sensitization resulted in higher ABO-adjusted cPRA relative to conventional cPRA by HLA alone, except for AB candidates since they are not ABO-sensitized. Within cPRA Point Group = 99%, 43% of the candidates moved up to ABO-adjusted cPRA Point Group = 100%, though this proportion varied substantially by candidate blood group. Nearly all O and most B candidates would have elevated ABO-adjusted cPRA values above this policy threshold for allocation priority, but relatively few A candidates displayed this shift. Overall, ABO-adjusted cPRA more accurately measures the proportion of immune-compatible donors compared with conventional HLA cPRA, especially for highly sensitized candidates. Implementation of this novel metric could enable the development of allocation policies permitting more ABO-compatible transplants without compromising equity.
Author Notes
  • James H. Lan, Vancouver Coastal Health Research Institute, Vancouver, Canada. Email: james.lan@vch.ca
Keywords
Research Categories
  • Health Sciences, Pathology

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