Risk assessment of antibody-mediated damage based on the detection of HLA and non-HLA antibodies toward extracellular antigens before kidney transplantation

Risk assessment of antibody-mediated damage based on the detection of HLA and non-HLA antibodies toward extracellular antigens before kidney transplantation

IntroductionDonor-specific human leukocyte antigens antibodies (HLA-DSA) contribute toantibody-mediated rejection (ABMR) after kidney transplantation (KT). Non-HLA antibodies may play a role in ABMR in the presence of HLA-DSA or the development of microvascular inflammation (MVI) in its absence. Con...

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Main Authors: Eulàlia Solà-Porta, Dolores Redondo-Pachón, Jorge Eguía-Núñez, Anna Buxeda, José Luís Caro, Javier Gimeno, Luís Campuzano, Carla Burballa, Betty Chamoun, Sara Sanz-Ureña, Judith Federico-Vega, Elisenda Alari-Pahissa, Julio Pascual, María José Pérez-Sáez, Marta Crespo
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Immunology
Subjects:
non-HLA antibodies
HLA
ABMR
antibody-mediated rejection
MVI
microvascular inflammation
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1614408/full
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Summary:IntroductionDonor-specific human leukocyte antigens antibodies (HLA-DSA) contribute toantibody-mediated rejection (ABMR) after kidney transplantation (KT). Non-HLA antibodies may play a role in ABMR in the presence of HLA-DSA or the development of microvascular inflammation (MVI) in its absence. Considering both types of antibodies in potential recipients could enhance ABMR/MVI risk assessment.MethodsWe present a case-control study of 121 KT recipients, 46 with ABMR/ MVI diagnosis, and 75 control cases with available sera before and after KT, follow-up HLA antibody monitoring, and biopsies. We determined 60 serum non-HLA antibodies using a multiplex test with an established cutoff. We evaluated their association with ABMR/MVI using a sample median fluorescence intensity (MFI) ratio sum.ResultsFollowing commercial cutoffs, non-HLA antibodies were detected in 87% of the patients before KT. We found that a high non-HLA antibody MFI ratio sum before KT and at biopsy were associated with an increased risk of ABMR/MVI, independently of HLA sensitization or HLA-DSA (OR = 1.039, p = 0.014 and OR = 1.036, p = 0.024). Antibodies against extracellular non-HLA antigens were associated with ABMR/MVI before KT (OR = 1.053, p = 0.040), but at diagnosis, only antibodies against intracellular non-HLA antigens were associated (OR = 1.062, p = 0.018).ConclusionThese findings suggest that non-HLA antibody assessment offers valuable complementary information, regardless of HLA sensitization, though appropriate cut-offs should be explored.
ISSN:1664-3224

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