How to cite this article: Battiwalla M, Hepgur M, Pan D, McCarthy PL, Ahluwalia MS, Camacho SH, Starostik P, Wallace PK. Multiparameter flow cytometry for the diagnosis and monitoring of small GPI-deficient cellular populations. Cytometry Part B 2010; 78B: 348–356.
Multiparameter flow cytometry for the diagnosis and monitoring of small GPI-deficient cellular populations†
Article first published online: 7 JUN 2010
Copyright © 2010 International Clinical Cytometry Society
Cytometry Part B: Clinical Cytometry
Volume 78B, Issue 5, pages 348–356, September 2010
How to Cite
Battiwalla, M., Hepgur, M., Pan, D., McCarthy, P. L., Ahluwalia, M. S., Camacho, S. H., Starostik, P. and Wallace, P. K. (2010), Multiparameter flow cytometry for the diagnosis and monitoring of small GPI-deficient cellular populations. Cytometry, 78B: 348–356. doi: 10.1002/cyto.b.20519
- Issue published online: 25 AUG 2010
- Article first published online: 7 JUN 2010
- Manuscript Accepted: 22 FEB 2010
- Manuscript Received: 31 AUG 2009
- NIH Shared Instrument Program
- Core Grant from the National Cancer Institute to the Roswell Park Cancer Institute. Grant Number: 5 P30 CA016056-29
- flow cytometry;
Glycosyl-phosphatidylinositol (GPI)-negative blood cells are diagnostic for Paroxysmal Nocturnal Hemoglobinuria (PNH). Marrow failure states are often associated with GPI-negative cell populations. Quantification of small clonal populations of GPI-negative cells influences clinical decisions to administer immunosuppressive therapy in marrow failure states (aplastic anemia or myelodysplastic syndrome) and to monitor minimal residual disease after allogeneic blood or marrow transplantation (BMT). We studied the reliability of high-resolution flow cytometry markers operating at the limits of detection.
We performed serial quantification of the PNH clone size in 38 samples using multiparameter flow cytometry. Granulocytes, monocytes, and RBCs were gated using forward and side scatter as well as lineage-specific markers. The GPI-linked markers fluorescent aerolysin (FLAER), CD55, and CD59 were comparatively evaluated. We also evaluated CD16 on granulocytes and CD14 on monocytes. The sensitivity of detection by each marker was further defined by serial dilution experiments on a flow-sorted sample. Two patients had quantification of their GPI-negative clones before and after allogeneic BMT.
FLAER was the most discriminant marker and allowed identification of 0.1% of GPI-negative cells despite other markers having superior signal-to-noise characteristics. CD14 and CD16 were inferior to CD55 at lower concentrations and in clinical application.
Multiparameter flow cytometry permits quantification of small GPI-negative clones with a sensitivity limit of about 0.1%. The single most reliable marker to monitor small granulocyte or monocyte PNH clones is FLAER, especially in conditions such as myelodysplastic syndromes or BMT, when traditional GPI-linked surface marker expression can be significantly altered. © 2010 International Clinical Cytometry Society