An easy and sensitive method to profile the antibody specificities of HLA-specific memory b cells

Gonca E. Karahan*, Juliette Krop, Caroline Wehmeier, Yvonne J.H. De Vaal, Janneke Langerak-Langerak, Dave L. Roelen, Neubury M. Lardy, Frederike J. Bemelman, Ineke J.M. Ten Berge, Marlies E.J. Reinders, Cees Van Kooten, Frans H.J. Claas, Sebastiaan Heidt

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

24 Citations (Scopus)
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Background. Pretransplant immunological risk assessment is currently based on donor-specific HLA antibodies in serum. Despite being an excellent source for antibodies produced by bone marrow-residing plasma cells, serum analysis does not provide information on the memory B-cell compartment. Although B-cell culture supernatants can be used to detect memory B cell-derived HLA antibodies, low IgG concentrations can preclude detectability of HLA antibodies in luminex single-antigen bead (SAB) assays. Methods. Culture supernatants of polyclonally activated B cells from alloantigen exposed (n = 13) or nonexposed (n = 10) individuals were either concentrated 10-fold, or IgG was isolated by using a protein G affinity purification method to increase the IgG concentration. These processed culture supernatants, as well as paired serum samples were tested for the presence of HLA antibodies using luminex SAB analysis. Results. In immunized individuals, 64% were found to have HLA-specific B-cell memory in concentrated supernatants, whereas 82% showed HLA-specific B-cell memory when IgG isolated supernatants were used for HLA antibody detection. IgG-isolated supernatants showed higher mean fluorescence intensity values compared with concentrated supernatants without increased background. In some individuals, HLA-specific B-cell memory was detected in the absence of accompanying serum antibody specificities. Conclusions. We developed a novel, highly sensitive method to assess the HLA-specific memory B-cell compartment using luminex SAB technology. This assay allows direct comparison to the serum compartment and may therefore provide a more complete picture of the humoral alloimmune response in patients with a history of alloantigen exposure.

Original languageEnglish
Pages (from-to)716-723
Number of pages8
Issue number4
Publication statusPublished - Apr 2019
Externally publishedYes

Bibliographical note

Funding Information:
1Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands. 2Department of Immunogenetics, Sanquin Diagnostic Services, Amsterdam, The Netherlands. 3Renal Transplant Unit, Department of Nephrology, Academic Medical Center, Amsterdam, The Netherlands. 4Department of Internal Medicine (Nephrology), Leiden University Medical Center, Leiden, The Netherlands. The authors declare no conflicts of interest. National Reference Center for Histocompatibility Testing, the Netherlands and the Dutch Transplant Society Astellas Transplantation Research Award 2017. CW was funded by the Swiss National Science Foundation. G.E.K. designed the study, performed experiments, analyzed data, wrote article. J.K., Yd.V., J.L.L. performed experiments. C.W. performed the

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