ArticleFrontiers in immunology2026
Non-HLA antibody trajectories may predict kidney transplant outcomes.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Understanding the role of non-HLA antibodies in kidney transplantation: a literature review.Frontiers in immunology · 2026Review
- Beyond HLA: an exploratory pilot study of non-HLA antibodies, HLA sensitization, and GSTT1 genotype in platelet transfusion refractoriness.Frontiers in immunology · 2026Article
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Donor-specific HLA antibodies (DSAs) are well-established mediators of antibody-mediated rejection (AMR), but growing evidence suggests that non-HLA antibodies may also contribute to kidney allograft dysfunction. However, the clinical utility of non-HLA antibody testing remains limited due to assay variability and undefined pathogenic thresholds. Methods: In this longitudinal study, we evaluated 167 deceased-donor kidney transplant recipients at UCSF using a multiplex Luminex assay to quantify IgG reactivity against 88 non-HLA antigens in paired pre- and post-transplant serum samples (n = 334). Patients were stratified by HLA-DSA status and graft outcome. The non-HLA panel reactive antibody (PRA) percentage was defined as the proportion of positive beads among the 88 tested antigens. Results: Global non-HLA PRA declined significantly from pre- to post-transplant (9% to 6%; Discussion: These findings suggest that longitudinal trajectories of non-HLA PRA, rather than staticmeasurements or DSA status alone, may influence graft loss. The dynamic nature of non-HLA antibody responses and supports integration of non-HLA antibody profiling into longitudinal immune monitoring frameworks. Larger multicenter studies are needed to define clinically meaningful threshold and estabilish the utility of non-HLA PRA testing across diverse transplant populations.
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