A2/A2B to B kidney transplantation outcomes: A single center 7‐year experience

Author:

El Chediak Alissar1ORCID,Shawar Saed2ORCID,Fallahzadeh Mohammad K.3ORCID,Forbes Rachel4ORCID,Schaefer Heidi M.2ORCID,Feurer Irene D.5ORCID,Rega Scott6ORCID,Triozzi Jefferson L.2ORCID,Shaffer David4ORCID

Affiliation:

1. Department of Internal Medicine Division of Nephrology University of Texas Southwestern Medical Center Dallas Texas USA

2. Department of Medicine Division of Kidney and Pancreas Transplant Vanderbilt University Medical Center Nashville Tennessee USA

3. Division of Nephrology Emory Transplant Center Emory University School of Medicine Atlanta Georgia USA

4. Department of Surgery Division of Kidney and Pancreas Transplant Vanderbilt University Medical Center Nashville Tennessee USA

5. Department of Surgery Department of Biostatistics Vanderbilt University Medical Center Nashville Tennessee USA

6. Vanderbilt Transplant Center Nashville Tennessee USA

Abstract

AbstractIntroductionData on long‐term outcomes following A2/A2B to B kidney transplants since the 2014 kidney allocation system (KAS) changes are few. The primary aim of this study is to report our 7‐year experience with A2/A2B to B kidney transplants and to compare post‐transplant outcomes of A2/A2B to a concurrent group of B to B kidney transplants. Additionally, the study evaluates the impact of pre‐transplant anti‐A1 titers on survival outcomes in A2/A2B transplants.MethodsThis retrospective, single‐center analysis included all adults who received A2/A2B to B deceased donor kidney transplants from December 2014 to June 2021 compared to B to B recipients. The effects of pre‐transplant IgM/IgG titers, stratified as ≤1:8 and ≥1:16, on death‐censored, rejection‐free, and overall graft survival were tested.ResultsFifty‐three A2/A2B and 114 B to B adults were included with a median follow‐up time of 32 months. Overall graft survival, patient survival, and rejection‐free graft survival did not differ between the two groups. There were no differences between the groups’ overall kidney function values (p > .80) or their temporal trajectories (time by group interaction p > .11). Unadjusted death‐censored graft survival was lower in A2/A2B to B compared to B recipients (p = .03), but the effect was not significant (p = .195) after adjusting for any readmissions (p = .96), rejection episodes (p < .001) or BK infection (p = .76). We did not detect an effect of pre‐transplant titer group on death‐censored (p = .59), rejection‐free (p = .61), or overall graft survival (p = .26)ConclusionsA2/A2B to B kidney transplants have comparable overall patient and graft survival, rejection‐free graft survival, and longitudinal renal function compared to B to B transplants at our center. Allograft survival outcomes were not significantly different between patients with low and high pre‐transplant anti‐A1 IgM/IgG titers.

Funder

National Center for Advancing Translational Sciences

National Institutes of Health

Publisher

Wiley

Reference27 articles.

1. OPTN/SRTR 2015 Annual Data Report: Kidney

2. Blood group ABO‐incompatible kidney transplantation biochemical and immunochemical studies of blood group A glycolipid antigens in human kidney and characterization of the antibody response (antigen specificity and antibody class) in O recipients receiving A2 grafts;Breimer ME;Transplant Proc,1987

3. Blood Group A and B Antigen Expression in Human Kidneys Correlated to A1/A2/B, Lewis, and Secretor Status

4. Improving Access to Kidney Transplantation without Decreasing Graft Survival: Long-Term Outcomes of Blood Group A2/A2B Deceased Donor Kidneys in B Recipients

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