Literature DB >> 32647428

FLAER Based Assay According to Newer Guidelines Increases Sensitivity of PNH Clone Detection.

Prabhu Manivannan1, Seema Tyagi2, Hara Prasad Pati2, Renu Saxena2.   

Abstract

Flow cytometry has become 'gold standard' for detecting abnormal clones in paroxysmal nocturnal hemoglobinuria (PNH), aplastic anemia (AA) and myelodysplastic syndrome (MDS). This pilot study was conducted in 2015 with a primary aim to evaluate the utility of single tube fluorescent aerolysin (FLAER) based testing and its comparison with two tubes non-FLAER based testing (CD55, CD59, CD24 and CD66b) in detecting abnormal PNH clones in these newly diagnosed cases. The secondary aim was an attempt to distinguish PNH from AA/MDS cases associated with PNH clones based on clinical, laboratory features and clone size at diagnosis. In this study, the abnormal PNH clones were detected using a single tube FLAER based testing and two tubes non-FLAER based testing in all cases of PNH (n = 12), healthy subjects (n = 18) and AA/MDS with PNH clone (n = 9) and compared with clinical and laboratory features at diagnosis. The receiver operator curve (ROC) analysis defined the optimal cut-offs for FLAER in granulocytes (> 0.7%) and monocytes (> 0.9%). There was significant positive correlation between FLAER and non-FLAER based testing in these cells (r > 0.3 and p < 0.05). FLAER based testing helped us in picking up smaller clones which were missed by latter technique in four patients thereby increasing its sensitivity and also technically proved to be cost-effective (Rs. 1800 vs. Rs. 2100). Even in PNH patients, the clone size was slightly higher by using FLAER when compared to non-FLAER based antibodies panel. The clone size of monocytes was always higher than granulocytes in both PNH and AA/MDS groups. Bone marrow cellularity and mean size of granulocytes and monocytes clone at diagnosis showed a striking statistically significant 'p' value of < 0.0001 between these groups. In this pilot study, a single tube FLAER based PNH testing had improved clone detection in all cases of PNH, AA/MDS with PNH clones. The clone size was > 30% in majority of PNH cases whereas in AA/MDS, it was usually < 10% at diagnosis. Hence this newer technique not only increased the sensitivity of PNH clone detection but also proved to be cost-effective. © Indian Society of Hematology and Blood Transfusion 2019.

Entities:  

Keywords:  Aplastic anemia; FLAER; Myelodysplastic syndrome; Paroxysmal nocturnal hemoglobinuria

Year:  2019        PMID: 32647428      PMCID: PMC7326856          DOI: 10.1007/s12288-019-01220-8

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN: 0971-4502            Impact factor:   0.900


  20 in total

1.  Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry.

Authors:  Michael J Borowitz; Fiona E Craig; Joseph A Digiuseppe; Andrea J Illingworth; Wendell Rosse; D Robert Sutherland; Carl T Wittwer; Stephen J Richards
Journal:  Cytometry B Clin Cytom       Date:  2010-07       Impact factor: 3.058

2.  Investigation of the survival of paroxysmal nocturnal hemoglobinuria red cells through the immunophenotyping of reticulocytes.

Authors:  J M Navenot; J Y Muller; D Blanchard
Journal:  Transfusion       Date:  1998-04       Impact factor: 3.157

3.  ICCS/ESCCA consensus guidelines to detect GPI-deficient cells in paroxysmal nocturnal hemoglobinuria (PNH) and related disorders part 3 - data analysis, reporting and case studies.

Authors:  Andrea Illingworth; Iuri Marinov; D Robert Sutherland; Orianne Wagner-Ballon; Luigi DelVecchio
Journal:  Cytometry B Clin Cytom       Date:  2018-01       Impact factor: 3.058

4.  PIG-A mutations in normal hematopoiesis.

Authors:  Rong Hu; Galina L Mukhina; Steven Piantadosi; Jamie P Barber; Richard J Jones; Robert A Brodsky
Journal:  Blood       Date:  2005-02-01       Impact factor: 22.113

5.  Practical guidelines for the high-sensitivity detection and monitoring of paroxysmal nocturnal hemoglobinuria clones by flow cytometry.

Authors:  D Robert Sutherland; Michael Keeney; Andrea Illingworth
Journal:  Cytometry B Clin Cytom       Date:  2012-04-25       Impact factor: 3.058

6.  Natural history of paroxysmal nocturnal haemoglobinuria using modern diagnostic assays.

Authors:  Victor M Moyo; Galina L Mukhina; Elizabeth S Garrett; Robert A Brodsky
Journal:  Br J Haematol       Date:  2004-07       Impact factor: 6.998

7.  Diagnosing PNH with FLAER and multiparameter flow cytometry.

Authors:  D Robert Sutherland; Nancy Kuek; Jeff Davidson; David Barth; Hong Chang; Erik Yeo; Sylvia Bamford; Ian Chin-Yee; Michael Keeney
Journal:  Cytometry B Clin Cytom       Date:  2007-05       Impact factor: 3.058

8.  Incidence of aplastic anemia: the relevance of diagnostic criteria. By the International Agranulocytosis and Aplastic Anemia Study.

Authors: 
Journal:  Blood       Date:  1987-12       Impact factor: 22.113

9.  Paroxysmal nocturnal hemoglobinuria: natural history of disease subcategories.

Authors:  Régis Peffault de Latour; Jean Yves Mary; Célia Salanoubat; Louis Terriou; Gabriel Etienne; Mohamad Mohty; Sophie Roth; Sophie de Guibert; Sebastien Maury; Jean Yves Cahn; Gerard Socié
Journal:  Blood       Date:  2008-06-05       Impact factor: 22.113

Review 10.  Recent advances in the diagnosis, monitoring, and management of patients with paroxysmal nocturnal hemoglobinuria.

Authors:  Stephen J Richards; Anita Hill; Peter Hillmen
Journal:  Cytometry B Clin Cytom       Date:  2007-09       Impact factor: 3.058

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  1 in total

1.  CD157 Can Replace CD24 and CD14 in a Single-Tube Flow-Cytometric Assay to Detect Paroxysmal Nocturnal Hemoglobinuria (PNH) Clones on Both Neutrophils and Monocytes: A Prospective Study From North India.

Authors:  Roopam Deka; Hara P Pati; Dinesh Chandra; Prabhu Manivannan; Richa Chauhan; Seema Tyagi; Renu Saxena
Journal:  Cureus       Date:  2022-04-08
  1 in total

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