The Most Common HLA Alleles and Anti-HLA Antibodies to Know for Virtual Cross-Match

dc.contributor.authorBasturk, Bilkay
dc.contributor.authorKantaroglu, Bircan
dc.contributor.authorKavuzlu, Miray
dc.contributor.authorKavuzlu, Miray
dc.contributor.authorSariturk, Cagla
dc.contributor.orcID0000-0002-8784-1974en_US
dc.contributor.orcID0000-0002-9288-942Xen_US
dc.contributor.orcID0000-0002-9288-942Xen_US
dc.contributor.orcID0000-0002-4130-1059en_US
dc.contributor.pubmedID27805512en_US
dc.contributor.researcherIDAAD-6918-2021en_US
dc.contributor.researcherIDAAE-2689-2021en_US
dc.contributor.researcherIDAAE-2689-2021en_US
dc.contributor.researcherIDAAS-7129-2021en_US
dc.date.accessioned2023-06-15T11:00:13Z
dc.date.available2023-06-15T11:00:13Z
dc.date.issued2016
dc.description.abstractObjectives: Human leukocyte antigens and HLA-specific antibodies are important before and after transplant treatment. The determination of the alloantibodies before transplant is useful for the estimation of risk for antibody-mediated rejection. Virtual crossmatch uses solid-phase assay to detect anti-HLA antibodies and allows exclusion of donors with unacceptable HLA antigens. The aim of our retrospective study was to investigate HLA class I and class II alleles and panel reactive antibody and Luminex Corporation (Austin, TX, USA) single-antigen bead assay positivity frequencies in the Southeastern region of Turkey Material and Methods: Tissue typing results for HLA class I (HLA-A, HLA-B, HLA-C) and class-II (DRB1and DQB1 haplotypes) in 1756 patients and 2951 donors who were at Baskent University Adana Research and Medical Center between 2010 and 2015 for transplant were studied using sequence-specific primers and/or sequence-specific oligonucleotides. Serum samples were analyzed by Luminex bead technology for antibody detection. Results: We found that, for class I, HLA-A*02, HLA-B*35, and HLA-A*24 and, for class II, DRB*11, DRB*01, and DRB*04 were the 4 most common antigens and HLA-A02, B49, A68, B7 were the 3 most common anti-HLA antibodies, with mean fluorescence intensity values >= 2000 in our population group. Human leukocyte antigen alleles and anti-HLA antibodies were compared with each other except HLA-A*02, A2, with no correlations between allele and panel reactive antibody frequencies identified. However, there was a weak correlation between panel reactive anti body-mean fluorescence intensity scores of 5000 and above with Luminex single-antigen bead assay. Conclusions: This study is the first to conduct such a mass screening of a Turkish population. Our study results show that there is no correlation between HLA frequencies and anti-HLA antibody frequencies. However, there was a weak correlation between panel reactive antibody mean fluorescence intensity scores of 5000 and above with Luminex single-antigen bead assay. Of note, this pattern is important to know for virtual cross-match.en_US
dc.identifier.endpage55en_US
dc.identifier.issn1304-0855en_US
dc.identifier.issueSupplement 3en_US
dc.identifier.scopus2-s2.0-85021848650en_US
dc.identifier.startpage53en_US
dc.identifier.urihttp://hdl.handle.net/11727/9620
dc.identifier.volume14en_US
dc.identifier.wos000398457600012en_US
dc.language.isoengen_US
dc.relation.isversionof10.6002/ect.tondtdtd2016.P5en_US
dc.relation.journalEXPERIMENTAL AND CLINICAL TRANSPLANTATIONen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPanel reactive antibodyen_US
dc.subjectSingle antigenen_US
dc.subjectRejectionen_US
dc.titleThe Most Common HLA Alleles and Anti-HLA Antibodies to Know for Virtual Cross-Matchen_US
dc.typearticleen_US

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