CC BY-NC-ND 4.0 · Ibnosina Journal of Medicine and Biomedical Sciences 2009; 01(01): 7-15
DOI: 10.4103/1947-489X.211051
Original Article

Even a single, remotely positive post-transplant alloantibody test correlates with increased chronic allograft nephropathy and graft loss after kidney transplantation

Ronald Pelletier
1,2,3,4,6   Comprehensive Transplant Center, The Ohio State University Medical Centers, Columbus, Ohio
,
Gregg Hadley
1,2,3,4,6   Comprehensive Transplant Center, The Ohio State University Medical Centers, Columbus, Ohio
,
Patrick Adams
1,2,3,4,6   Comprehensive Transplant Center, The Ohio State University Medical Centers, Columbus, Ohio
,
Mitchell Henry
1,2,3,4,6   Comprehensive Transplant Center, The Ohio State University Medical Centers, Columbus, Ohio
,
Zhangsheng Yu
5   Division of Biostatistics, The Ohio State University College of Public Health, Columbus, Ohio
,
Ronald Ferguson
1,2,3,4,6   Comprehensive Transplant Center, The Ohio State University Medical Centers, Columbus, Ohio
› Author Affiliations

Abstract

Background: Chronic renal allograft loss is considered as immunologically mediated when donor-specific alloantibodies are detected. However, remotely detected alloantibodies with lack of detection more proximate to graft loss occurrence may obscure the humoral association with graft damage.

Methods: We retrospectively reviewed 609 patients multiply tested post-transplant for detectable alloantibodies and correlated their results with clinical outcomes.

Results: Most patients had no detectable post-transplant alloantibodies (Group 1, n = 393), some converted from nondetectable to detectable alloantibodies (Group 2, n = 97), some always had detectable post-transplant alloantibodies (Group 3, n = 69), and some demonstrated alloantibodies that subsequently became undetectable (Group 4, n = 50). The incidence of death-censored graft survival for Group 4 patients was similar to Group 2 and 3 patients, and greater than Group 1 patients. Further, interstitial fibrosis/tubularatrophy (IF/TA) free survival was significantly worse (p=0.018) for Group 4 versus Group 1 recipients. Also, Group 4 versus Group 1 IF/TA-free survival was worse when recipients were regrouped based solely on anti-HLA class II (p=0.006), but not anti-HLA class I (p=ns) antibodies.

Conclusions: Detectable anti-HLA antibodies, even remotely, post-transplant identifies recipients at greater risk for IF/TA associated graft loss when compared to patients without detectable alloantibodies.



Publication History

Received: 15 May 2009

Accepted: 10 July 2009

Article published online:
23 May 2022

© 2009. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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