Functional and phenotypic profiles of HLA-specific antibodies in relation to antibody-mediated kidney transplant rejection
- PMID: 39889319
- PMCID: PMC11922655
- DOI: 10.1016/j.humimm.2025.111247
Functional and phenotypic profiles of HLA-specific antibodies in relation to antibody-mediated kidney transplant rejection
Abstract
Donor Specific Antibodies (DSAs) are associated with a higher risk of Antibody Mediated Rejection (AMR). However, not all DSAs are pathogenic, and patients that raise DSAs have a wide spectrum of outcomes ranging from the complete absence of graft injury to severe AMR. Hence, characterization of both the qualitative features and titer of DSAs has the potential to predict AMR risk and treatment outcome for sensitized patients. Here, using HLA-A2+ cell-based assays, we investigate the qualitative features of immunoglobulin G (IgG) alloantibodies including Fc receptor binding properties and Fc-mediated effector function over time. Compared to seronegative controls, reactive antibodies in seropositive participants were predominantly IgG1, and exhibited elevated levels of binding to the receptors involved in Antibody Dependent Cellular Phagocytosis (ADCP) and Antibody Dependent Cellular Cytotoxicity (ADCC) activity. Further analysis of seropositive individuals revealed that these activities were predictive ofAMR status. Collectively, these results suggest a role for phagocytic and cytotoxic antibody effector functions of DSA in contributing to graft injury.
Keywords: Donor specific antibodies; Effector function; Kidney transplant; NK cells; Phagocytosis.
Copyright © 2025 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: P.B., S.S., A.L.M., A.M., and M.E.A. has patent pending to Dartmouth College. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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