Unexpected interference in cell surface staining by monoclonal antibodies to unrelated antigens. Issue 5 (20th October 2014)

• Record Type: Journal Article
• Authors: De Vita, Martina; Catzola, Valentina; Buzzonetti, Alexia; Fossati, Marco; Battaglia, Alessandra; Zamai, Loris; Fattorossi, Andrea
• Is Part Of: Cytometry. Volume 88:Issue 5(2015)
• Page Start: 352
• Page End: 354
• Publication Date: 2014-10-20
• Subjects: immunophenotyping -- steric hindrance -- quenching -- flow cytometry; Flow cytometry -- Diagnostic use -- Periodicals; Cytodiagnosis -- Periodicals; 616.07582
• DOI: 10.1002/cyto.b.21197
• Languages: English
• ISSNs: 1552-4949

Abstract

Abstract : Background: The possible occurrence of an erroneous immunophenotyping due to interference between monoclonal antibodies (MoAbs) is often overlooked when the epitopes are assumed to be not close to each other. This is particularly important when exploring immune cell populations whose identification is still investigational. The commonly held view is that myeloid derived suppressor cells can be identified as either HLA‐DR neg/dim cells or interleukin‐4 receptor‐α (CD124) + cells among peripheral blood monocytes. We made the serendipitous observation that the fluorescence signal provided by the PE‐CD124 MoAb was attenuated when the PE‐CF594‐HLA‐DR MoAb was added to the staining tube. Methods: Peripheral blood mononuclear cells from healthy donors were stained with the PE‐CD124 MoAb and, as control, PE ‐CD40, ‐CD4 and ‐CD14, and either the PE‐CF594‐HLA‐DR MoAb or its unlabeled form. B cells, which also express CD124, were analyzed for comparison. Results: The PE‐CF594‐HLA‐DR MoAb but not its unlabeled form reduced PE‐CD124 MoAb staining on monocytes and B cells. No other monocyte and B cell surface marker staining was affected by the PE‐CF594‐HLA‐DR MoAb. The PE‐CF594‐HLA‐DR MoAb interfered with the PE‐CD124 MoAb likely because of steric hindrance by bulky fluorochromes, although a quenching due to fluorescence resonance energy transfer might also cooperate to the PE‐CD124 MoAb staining attenuation. Conclusions: Present observations highlight the importance of interference between MoAbs as a source of error when analyzing multicolor flow cytometry data. © 2014 International Clinical Cytometry Society