Significance of the intraindividual variability of HLA IgG antibodies in renal disease patients observed with different beadsets monitored with two different secondary antibodies on a Luminex platform
Autor: | Edward J. Filippone, Susan L. Saidman, Carly Callender, Mepur H. Ravindranath, Grace K. Mahowald, Adarsh Babu, Soldano Ferrone |
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Rok vydání: | 2018 |
Předmět: |
Allergy
Immunology Human leukocyte antigen IgHPolyFab: MFI: mean fluorescent intensity (MFI) 030230 surgery Antibodies 03 medical and health sciences 0302 clinical medicine Calculated panel reactive antibody (cPRA) Antigen Heavy chain HLA Antigens Isoantibodies medicine Humans Single antigen bead assays (SAB) Renal Insufficiency Chronic Sensitization β2-microglobulin Observer Variation biology business.industry Beta-2 microglobulin Panel reactive antibody FcMonoIgG medicine.disease Kidney Transplantation Primary and secondary antibodies Denatured antigen medicine.anatomical_structure Histocompatibility Immunoglobulin G biology.protein Original Article Antibody business Epitope Mapping 030215 immunology |
Zdroj: | Immunologic Research |
ISSN: | 1559-0755 0257-277X |
DOI: | 10.1007/s12026-018-9027-2 |
Popis: | The accurate measurement of anti-HLA alloantibodies in transplant candidates is required for determining the degree of sensitization and for the listing of unacceptable antigens for organ allocation. Both the configuration of the HLA molecules coated on the beads and the nature of detection antibodies may impede assessment of the presence and strength of anti-HLA IgG- with the Luminex single-antigen-bead assay. Sera antibodies of the end-stage renal disease patients were compared using LIFECODES (LC) and LABScreen (LS) beadsets monitored with polyclonal-Fab (IgHPolyFab) and monoclonal-IgG (FcMonoIgG) second antibodies. Positive results at mean fluorescence intensity (MFI) > 500 (at serum dilution 1/10) were used to calculate panel reactive antibody (cPRA) levels. LS-beadsets are coated with monomeric variants in addition to intact HLA antigens with or without peptides, while LC-beadsets are devoid of monomeric variants and with lesser levels of peptide-free heterodimers. Consequently, IgG antibodies against both classes of HLA were reactive to more antigens with LS than with LC-beadsets. For both classes, MFIs were also frequently higher with LS than with LC. For HLA-I, MFIs were higher with IgHPolyFab than with FcMonoIgG with the exception of sera with MFIs > 5000 where they were comparable. For HLA-II, the reverse occurred, with significantly higher levels with FcMonoIgG regardless of the beadsets. The intraindividual variability observed between beadsets with two detection antibodies elucidates that antigens found as acceptable with one beadset may end up unacceptable with the other beadsets, with the possibility of denying potentially compatible transplants to candidates. |
Databáze: | OpenAIRE |
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