| Literature DB >> 32190967 |
Sarah B See1, Benjamin S Mantell1,2, Kevin J Clerkin3, Bryan Ray4, E Rodica Vasilescu5, Charles C Marboe5, Yoshifumi Naka6, Susan Restaino3, Paolo C Colombo2, Linda J Addonizio2, Maryjane A Farr3, Emmanuel Zorn1.
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.Entities:
Keywords: B cell biology; alloantibody; autoantibody; autoantigen; basic (laboratory) research/science; heart transplantation/cardiology; immunobiology; rejection: antibody-mediated (ABMR)
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Year: 2020 PMID: 32190967 PMCID: PMC8117249 DOI: 10.1111/ajt.15871
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086