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Frequency and Perturbations of Various Peripheral Blood Cell Populations Before and After Eculizumab Treatment in Paroxysmal Nocturnal Hemoglobinuria

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Specialty Hematology
Date 2020 Dec 20
PMID 33341510
Citations 6
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Abstract

While red blood cells (RBCs) and granulocytes have been more studied, platelets and reticulocytes are not commonly used in paroxysmal nocturnal hemoglobinuria (PNH) flow-cytometry and less is known about susceptibility to complement-mediated destruction and effects of anti-complement therapy on these populations. We performed flow-cytometry of RBCs and granulocytes in 90 PNH patients and of platelets and reticulocytes in a subgroup (N = 36), to unveil perturbations of these populations during PNH disease course before and after anti-complement treatment. We found that platelets and reticulocytes were less sensitive to complement-mediated lysis than RBCs but not as resistant as granulocytes, as shown by mean sensitive fraction (difference in a given PNH population vs. PNH granulocyte clone size). In treated patients, reticulocytes, platelets, RBCs (with differences between type II and III) and granulocytes significantly increased post-treatment, confirming the role of PNH hematopoiesis within the context of anti-complement therapy. Moreover, we found that PNH platelet clone size reflects PNH granulocyte clone size. Finally, we established correlations between sensitive fraction of PNH cell-types and thrombosis. In sum, we applied a flow-cytometry panel for investigation of PNH peripheral blood populations' perturbations before and after eculizumab treatment to explore complement-sensitivity and kinetics of these cells during the disease course.

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References
1.
Iwamoto N, Kawaguchi T, Nagakura S, Hidaka M, Horikawa K, Kagimoto T . Markedly high population of affected reticulocytes negative for decay-accelerating factor and CD59 in paroxysmal nocturnal hemoglobinuria. Blood. 1995; 85(8):2228-32. View

2.
DeZern A, Dorr D, Brodsky R . Predictors of hemoglobin response to eculizumab therapy in paroxysmal nocturnal hemoglobinuria. Eur J Haematol. 2012; 90(1):16-24. PMC: 3673783. DOI: 10.1111/ejh.12021. View

3.
Hillmen P, Young N, Schubert J, Brodsky R, Socie G, Muus P . The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria. N Engl J Med. 2006; 355(12):1233-43. DOI: 10.1056/NEJMoa061648. View

4.
Borowitz M, Craig F, DiGiuseppe J, Illingworth A, Rosse W, Sutherland D . Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry. Cytometry B Clin Cytom. 2010; 78(4):211-30. DOI: 10.1002/cyto.b.20525. View

5.
Takeda J, Miyata T, Kawagoe K, Iida Y, Endo Y, Fujita T . Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell. 1993; 73(4):703-11. DOI: 10.1016/0092-8674(93)90250-t. View