AUTHOR=Solà-Porta Eulàlia , Redondo-Pachón Dolores , Eguía-Núñez Jorge , Buxeda Anna , Caro José Luís , Gimeno Javier , Campuzano Luís , Burballa Carla , Chamoun Betty , Sanz-Ureña Sara , Federico-Vega Judith , Alari-Pahissa Elisenda , Pascual Julio , Pérez-Sáez María José , Crespo Marta 

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

JOURNAL=Frontiers in Immunology

VOLUME=Volume 16 - 2025

YEAR=2025

URL=https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2025.1614408

DOI=10.3389/fimmu.2025.1614408

ISSN=1664-3224

ABSTRACT=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.