Specificity of HLA monoclonal antibodies and their use to determine HLA expression on lymphocytes and peripheral blood stem cells

Author:

Peton Benjamin1,Taniguchi Michiko2,Mangiola Massimo3,Al Malki Monzr M.4,Gendzekhadze Ketevan1

Affiliation:

1. HLA Laboratory, Department of Hematology and Hematopoietic Cell Transplantation City of Hope National Medical Center Duarte California USA

2. Department of Pathology and Laboratory Medicine, Lewis Katz School of Medicine Temple University Philadelphia Pennsylvania USA

3. Transplant Institute NYU Langone Medical Center New York New York USA

4. Department of Hematology and Hematopoietic Cell Transplantation City of Hope National Medical Center Duarte California USA

Abstract

HLA Class I and II expression are known to differ locus‐to‐locus, however, HLA expression on the cell‐surface is frequently reported as the total amount of HLA Class I or II antigens. This is despite evidence that indicates the differential expression of HLA can influence patient outcomes post‐transplantation. Although numerous commercially available HLA monoclonal antibodies (mAbs) exist to characterize HLA expression, there is currently a lack of detailed information regarding their reactivities to HLA specificities. The specificities of locus‐specific HLA mAbs (nine Class I and four Class II mAbs) were evaluated by two solid‐phase Luminex single antigen bead assays. The reactivity patterns of these mAbs were then confirmed by flow cytometry using lymphocytes and PBSCs (peripheral blood stem cells). Out of the 13 HLA mAbs tested, only four (one Class I and three Class II mAbs) displayed intra‐locus reactivity without also reacting to inter‐locus specificities. Epitope analysis revealed the presence of shared epitopes across numerous HLA loci, explaining much of the observed inter‐locus reactivity. The specificity of the HLA mAbs seen in solid‐phase assays was confirmed against PBSCs and lymphocytes by flow cytometry. Using this method, we observed differences in the cell surface expression of HLA‐C, HLA‐DR, HLA‐DQ, and HLA‐DP between PBSCs and lymphocytes. Our results emphasize the need to characterize the reactivity patterns of HLA mAbs using solid‐phase assays before their use on cells. Through understanding the reactivity of these HLA mAbs, the cellular expression of HLA can be more accurately assessed in downstream assays.

Publisher

Wiley

Subject

Genetics,Immunology,Immunology and Allergy

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