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Cytotoxicity and antibody binding by flow cytometry: A single assay to simultaneously assess two parameters
Author(s) -
Saw Chee L.,
Bray Robert A.,
Gebel Howard M.
Publication year - 2008
Publication title -
cytometry part b: clinical cytometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.646
H-Index - 61
eISSN - 1552-4957
pISSN - 1552-4949
DOI - 10.1002/cyto.b.20424
Subject(s) - cytotoxicity , complement dependent cytotoxicity , flow cytometry , antibody , human leukocyte antigen , immunology , antibody dependent cell mediated cytotoxicity , cytotoxic t cell , transplantation , antigen , microbiology and biotechnology , chemistry , biology , medicine , monoclonal antibody , in vitro , biochemistry
Background: Cell death, as determined by complement‐dependent cytotoxicity or antibody binding, as assessed by flow cytometry, are the two main methods histocompatibility laboratories use to identify HLA antibodies. Conventional cytotoxicity assays, even anti‐human globulin (AHG) enhanced, are relatively insensitive, subjective and require complement fixation. In contrast, antibody binding assays (e.g.: flow cytometry crossmatch, FCXM) are sensitive, objective, and complement independent. When sera from potential transplant recipients test positive by both methods, most centers would not proceed to transplant unless patients undergo desensitization. However, when the CDC crossmatch is negative but the FCXM positive, how or whether to proceed is controversial. Frequently, both assays are performed. Methods: In this study, we developed a comprehensive procedure that determines cell death, and antibody binding in a single assay: the cytotoxic flow crossmatch (cFCXM). The assay was validated in parallel studies with two other conventional methodologies, namely AHG and FCXM. Results: Using a combination of eight cells and 15 sera, we have determined an optimal method for the simultaneous detection of HLA antibody binding and cytotoxicity using a single platform. Additionally, we have identified three distinct patterns of HLA antibody reactivity: (1) AHG pos /cFCXM pos /FCXM pos , (2) AHG neg /cFCXM neg /FCXM pos , and (3) a previously unrecognized category, namely, AHG neg /cFCXM pos /FCXM pos . Conclusions: These studies document that cytotoxicity and antibody binding can be simultaneously assessed and marks the first demonstration of complement‐dependent HLA antibodies undetectable by conventional cytotoxicity. Routine application of this assay may provide new insights regarding transplantation of patients presenting as AHG neg /FCXM pos by classifying them according to their cFCXM status. © 2008 Clinical Cytometry Society