| Literature DB >> 28371365 |
G E Karahan1, Y J H de Vaal1, J Krop1, C Wehmeier1, D L Roelen1, F H J Claas1, S Heidt1.
Abstract
Humoral responses against mismatched donor HLA are routinely measured as serum HLA antibodies, which are mainly produced by bone marrow-residing plasma cells. Individuals with a history of alloimmunization but lacking serum antibodies may harbor circulating dormant memory B cells, which may rapidly become plasma cells on antigen reencounter. Currently available methods to detect HLA-specific memory B cells are scarce and insufficient in quantifying the complete donor-specific memory B cell response due to their dependence on synthetic HLA molecules. We present a highly sensitive and specific tool for quantifying donor-specific memory B cells in peripheral blood of individuals using cell lysates covering the complete HLA class I and class II repertoire of an individual. Using this enzyme-linked immunospot (ELISpot) assay, we found a median frequency of 31 HLA class I and 89 HLA class II-specific memory B cells per million IgG-producing cells directed at paternal HLA in peripheral blood samples from women (n = 22) with a history of pregnancy, using cell lysates from spouses. The donor-specific memory B cell ELISpot can be used in HLA diagnostic laboratories as a cross-match assay to quantify donor-specific memory B cells in patients with a history of sensitizing events.Entities:
Keywords: alloantibody; basic (laboratory) research/science; clinical research/practice; histocompatibility; immunobiology; major histocompatibility complex (MHC); organ transplantation in general
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Year: 2017 PMID: 28371365 DOI: 10.1111/ajt.14293
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086