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Profiling non-HLA antibody responses in antibody-mediated rejection following heart transplantation. | LitMetric

AI Article Synopsis

  • * In a study of 64 heart transplant recipients, the AMR group showed a higher presence of reactivity to non-HLA autoantigens compared to those without AMR and healthy controls, suggesting a link between these autoantibodies and graft rejection.
  • * Specific antigens, including vimentin and beta-tubulin, exhibited significantly different reactivity levels between AMR and non-AMR patients, with higher reactivity potentially correlating with graft failure, though the exact mechanisms remain unclear

Article Abstract

Antibody-mediated rejection (AMR) driven by the development of donor-specific antibodies (DSA) directed against mismatched donor human leukocyte antigen (HLA) is a major risk factor for graft loss in cardiac transplantation. Recently, the relevance of non-HLA antibodies has become more prominent as AMR can be diagnosed in the absence of circulating DSA. Here, we assessed a single-center cohort of 64 orthotopic heart transplant recipients transplanted between 1994 and 2014. Serum collected from patients with ≥ pAMR1 (n = 43) and non-AMR (n = 21) were tested for reactivity against a panel of 44 non-HLA autoantigens. The AMR group had a significantly greater percentage of patients with elevated reactivity to autoantigens compared to non-AMR (P = .002) and healthy controls (n = 94, P < .0001). DSA-positive AMR patients exhibited greater reactivity to autoantigens compared to DSA-negative (P < .0001) and AMR patients with DSA and PRA > 10% were identified as the subgroup with significantly elevated responses. Reactivity to 4 antigens, vimentin, beta-tubulin, lamin A/C, and apolipoprotein L2, was significantly different between AMR and non-AMR patients. Moreover, increased reactivity to these antigens was associated with graft failure. These results suggest that antibodies to non-HLA are associated with DSA-positive AMR although their specific role in mediating allograft injury is not yet understood.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117249PMC
http://dx.doi.org/10.1111/ajt.15871DOI Listing

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