Expression of glycosyl-phosphatidylinositol-linked glycoproteins in blood cells from paroxysmal nocturnal haemoglobinuria patients. A flow cytometry study using CD55, CD58 and CD59 monoclonal antibodies

Leukemia and Lymphoma

Volumn 21, Issue 1-2, 1996, Pages 143-151

  Navenot, J M ^a   Bernard, D ^a   Harousseau, J L ^b   Muller, J Y ^a   Blanchard, D ^a  

^a Centre Regional de Transfusion Sanguine   (France)

^b NANTES UNIVERSITY HOSPITAL   (France)

Author keywords

CD59; DAF; Flow cytometry; LFA 3; Paroxysmal nocturnal haemoglobinuria

Indexed keywords

CD59 ANTIGEN; DECAY ACCELERATING FACTOR; GLYCOPROTEIN; GLYCOSYLPHOSPHATIDYLINOSITOL; LYMPHOCYTE FUNCTION ASSOCIATED ANTIGEN 3; MEMBRANE PROTEIN; MONOCLONAL ANTIBODY;

ADOLESCENT; ADULT; AGED; APLASTIC ANEMIA; ARTICLE; BLOOD CELL; BLOOD TRANSFUSION; CLINICAL ARTICLE; CONTROLLED STUDY; ERYTHROCYTE; FEMALE; FLOW CYTOMETRY; GRANULOCYTE; HUMAN; LYMPHOCYTE; MALE; MONOCYTE; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PRIORITY JOURNAL; PROTEIN DEFICIENCY; THROMBOCYTE;

ADULT; AGED; AGED, 80 AND OVER; ANEMIA, APLASTIC; ANTIBODIES, MONOCLONAL; ANTIGENS, CD; ANTIGENS, CD55; ANTIGENS, CD58; ANTIGENS, CD59; ERYTHROCYTES; FEMALE; FLOW CYTOMETRY; GLYCOPROTEINS; GLYCOSYLPHOSPHATIDYLINOSITOLS; HEMOGLOBINURIA, PAROXYSMAL; HUMANS; MALE; MIDDLE AGED;

EID: 0030047751     PISSN: 10428194     EISSN: None     Source Type: Journal    
DOI: 10.3109/10428199609067592     Document Type: Article

References (34)

1. Rotoli, B. and Luzzatto, L. (1989) Paroxysmal nocturnal haemoglobinuria. Baillière's Clinical Haematology, 2, 113-138.
2. Miyata, T., Takeda, J., Iida, Y., Yamada, N., Inoue, N., Takahashi, M., Maeda, K., Kitani, T. and Kinoshita, T. (1993) The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science, 259, 1318-1320.
3. Takeda, J., Miyata, T., Kawagoe, K., Iida, Y., Endo, Y., Fujita, T., Takahashi, M., Kitani, T. and Kinoshita, T. (1993) Deficiency of the GPI anchor caused by somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell, 73, 703-711.
4. Rosse, W. F. (1990) Phosphatidylinositol-linked proteins and paroxysmal nocturnal haemoglobinuria. Blood, 75, 1595-1601.
5. Yomtovian, R., Prince, G. M. and Medof, M. E. (1993) The molecular basis for paroxysmal nocturnal haemoglobinuria. Transfusion, 33, 852-873.
6. Nicholson-Weller, A., Burge, S., Fearon, D. T., Weller, P. F. and Austen, K. F. (1982) Isolation of a human erythrocyte membrane glycoprotein with decay accelerating activity for C3 convertase of the complement system. Journal Immunology, 129, 184-9.
7. Holguin, M. H., Wilcox, L. A., Bernshaw, N. J., Rosse, W. F. and Parker, C. J. (1989) Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuria. Journal of Clinical Investigations, 84, 1387-1394.
8. Holguin, M. H., Martin, C. B., Bernshaw, N. J. and Parker, C. J. (1992) Analysis of the effects of activation of the alternative pathway of complement on erythrocytes with an isolated deficiency of decay accelerating factor. Journal of Immunology, 148, 498-502.
9. Telen, M. J. and Green, A. M. (1989) The Inab phenotype: Characterization of the membrane protein and complement regulatory defect. Blood, 74, 437-441.
10. Yamashina, M., Ueda, E., Kinoshita, T., Takami, T., Ojima, A., Ono, H., Tanaka, H., Kondo, N., Orii, T., Okada, N., Okada, H., Inoue, K. and Kitani, T. (1990) Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. New England Journal of Medicine, 323, 1184-9.
11. Navenot, J. M., Bernard, D., Petit-Frioux, Y. Loirat, M. J., Guimbretiere, J., Muller, J. Y. and Blanchard, D. (1993) Diagnostic rapide des hémoglobinuries nocturnes paroxystiques par agglutination en gel. Revue Française de Transfusion et d'Hémobiologie, 36, 135-147.
12. van der School, C. E.. Huizinga, T. W. J., van't Veer-Korthof, E. T., Wijmans, R., Pinkster, J. and von dem Borne, A. E. G.Kr. (1990) Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, description of a new diagnostic cytofluorometric assay. Blood, 76, 1853-9.
13. Schubert, J., Alvarado, M., Uciechowski, P., Zielinska-Skowronek, M., Freund, M., Vogt, H. and Schmidt, R. E. (1991) Diagnosis of paroxysmal nocturnal haemoglobinuria using immunophenotyping of peripheral blood cells. British Journal of Haematology, 79, 487-492.
14. Bessler, M. and Fehr, J. (1991) Fc III receptors (FcRIII) on granulocytes: A specific and sensitive diagnostic test for paroxysmal nocturnal hemoglobinuria (PNH). European Journal of Haematology, 47, 179-184.
15. Shichishima, T., Terasawa, T., Saitoh, Y., Hashimoto, C., Ohto, H. and Maruyama, Y. (1993) Diagnosis of paroxysmal nocturnal haemoglobinuria by phenotypic analysis of erythrocytes using two-colour flow cytometry with monoclonal antibodies to DAF and CD59/MACIF. British Journal of Haematology, 85, 378-386.
16. Sims, P. J., Faioni, E. M., Wiedmer, T. and Shattil, S. J. (1988) Complement proteins C5b-9 cause release of membrane vesicles from the platelet surface that are enriched in the membrane receptor for coagulation factor Va and express prothrombinase activity. Journal of Biological Chemistry, 263, 18205-18212.
17. Wiedmer, T., Hall, S. E., Ortel, T. L., Kane, W. H., Rosse, W. F. and Sims, P. J. (1993) Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuria. Blood, 82, 1192-6.
18. Selvaraj, P., Dustin, M. L., Silber, R., Low, M. G. and Springer, T. A. (1987) Deficiency of lymphocyte function-associated antigen 3 (LFA-3) in paroxysmal nocturnal hemoglobinuria. Functional correlates and evidence for a phosphatidylinositol membrane anchor. Journal of Experimental Medicine. 166, 1011-1025.
19. Dustin, M. L., Selvaraj, P., Mattaliano, R. J. and Springer, T. A. (1987) Anchoring mechanisms for LFA-3 cell adhesion glycoprotein at membrane surface. Nature, 329, 846-8.
20. Campbell, A. M. (1984) Monoclonal antibody technology. In Laboratory Techniques in Biochemistry and Molecular Biology, edited by R. H. Burdon and P. H. van Knippenberg, vol 13, Amsterdam: Elsevier Publisher.
21. Loirat, M. J., Dahr, W., Muller, J. Y. and Blanchard, D. (1994) Characterization of new murine monoclonal antibodies directed against glycophorins C and D. Transfusion Medicine, 4, 147-155.
22. AI plaquettaire par immunoblotting. Immunoanalyse Biologique Spécialisée, 34, 31-6.
23. Nicholson-Weller. A., March, J. P., Rosen, C. E., Spicer, D. B. and Austen, K. F. (1985) Surface membrane expression by human blood leukocytes and platelets of decay-accelerating factor, a regulatory protein of the complement system. Blood, 65, 1237-1244.
24. Terstappen, L. W. M. M., Nguyen, M., Lazarus, H. M. and Medof, M. E. (1992) Expression of the DAF (CD55) and CD59 antigens during normal hemalopoietic cell differentiation. Journal of Leukocyte Biology, 52, 652-660.
25. Oni, S. B., Osunkoya, B. O. and Luzzatlo, L. (1970) Paroxysmal nocturnal hemoglobinuria: Evidence for monoclonal origin of abnormal red cells. Blood, 36, 145-152.
26. Rosse, W. F. (1991) Editorial: Dr Ham's test revisited. Blood, 78, 547-550.
27. Schmidt, R. E. and Perussia, B. (1989) Cluster report: CD16. In Leukocyte typing IV, edited by W. Knapp, B. Dörken, W. R. Gilks, E. P. Rieber, R. E. Schmidt, H. Stein and A. E. G. Kr von dem Borne, pp. 574-8. Oxford University Press.
28. Rotoli, B., Bessler, M., Alfinito, F. and del Vecchio, L. (1993) Membrane proteins in paroxysmal nocturnal haemoglobinuria. Blood reviews, 7, 75-86.
29. Morgan, B. P. (1989) Complement membrane attack on nucleated cells: resistance, recovery and non-lethal effects. Biochemical Journal, 264, 1-14.
30. Miyata, T., Yamada, N., Iida, Y., Nishimura, J., Takeda, J., Kitani, T. and Kinoshita, T. (1994) Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria. New England Journal of Medicine, 330, 249-255.
31. Bessler, M., Mason, P. J., Hillmen, P., Miyata, T., Yamada, N., Takeda, J., Luzzatto, L. and Kinoshita, T. (1994) Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO Journal, 13, 110-7.
32. Ware, R. E., Rosse, W. F. and Howard, T. A. (1994) Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria. Blood, 83, 2418-2422.
33. Bessler, M., Mason, P., Hillmen, P. and Luzratto, L. (1994) Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet, 343, 951-3.
34. Rotoli, B. and Luzzatto, L. (1989) Paroxysmal nocturnal hemoglobinuria. Seminars in hematology, 26, 201-7.