F reticulocytes assay: A method to evaluate fetal hemoglobin production

Hemoglobin

Volumn 22, Issue 5-6, 1998, Pages 419-425

  Maier Redelsperger, M ^a,b   Elion, J ^b   Girot, R ^a,b  

^a HÔPITAL TENON   (France)

^b HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCEIN ISOTHIOCYANATE; HEMOGLOBIN F; HYDROXYUREA; MONOCLONAL ANTIBODY;

BLOOD SMEAR; CELL SURVIVAL; CHILD; CLINICAL ARTICLE; CONFERENCE PAPER; CONTROLLED STUDY; HEMOGLOBIN SYNTHESIS; HEMOGLOBINOPATHY; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE MICROSCOPY; LABORATORY TEST; RETICULOCYTE COUNT; SICKLE CELL ANEMIA;

EID: 0032421280     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630269809071540     Document Type: Conference Paper

References (19)

1. Boyer, S.H., Belding, T.K., Margolet, L., and Noyes, A.N.: Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults. Science, 188:361-363, 1975.
2. Stamatoyannopoulos, G., Papayannopoulou, Th., Brice, M., Kurachi, S., Nakamoto, B., Lim, G., and Farquhar, M.: Cell biology of hemoglobin switching. The switch from fetal to adult hemoglobin formation during ontogeny. In Hemoglobins in Development and Differentiation, edited by G. Stamatoyannopoulos and A.W. Nienhuis, pages 287-305, Alan R. Liss, Inc., New York, NY, USA, 1981.
3. Wood, W.G.: Increased Hb F in adult life. In The Hemoglobinopathies, edited by D.R. Higgs and D.J. Weatherall, Vol. 6, pages 177-213, Bailliere's Clinical Haematology, W.B. Saunders Company, London, UK, 1993.
4. Dover, G.J., Boyer, S.H., Charache, S., and Heintzelman, K.: Individual variation in the production and survival of F cells in sickle cell disease. N. Engl. J. Med., 299: 1428-1435, 1978.
5. Maier-Redelsperger, M. and Girat, R.: Les aspects cellulaires de la distribution et de la production de l'hémoglobine fœtale. Hématologie, 5:437-442, 1996.
6. Beuzard, Y. and Rosa, J.: Mise en évidence des globules rouges contenant de l'hémoglobine fœtale: Test de Kleihauer, in Techniques en Hématologie, second edition, edited by C. Sultan, G. Priolet, Y. Beuzard, J. Rosa, and F. Josso, page 146, Flammarion/Medecine-Sciences, Paris, 1978.
7. Dover, G.J., Boyer, S.H., and Bell, W.R.: Microscopic method for assaying F cell production: illustrating changes during aplastic anemia. Blood, 52:664-672, 1978.
8. Wood, W.G., Stamatoyannopoulos, G., Lim, G., and Nute, P.E.: F cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F. Blood, 46:671-687, 1975.
9. Papayannopoulou, T., Vichinsky, E., and Stamatoyannopoulos, G.: Fetal Hb production during acute erythroid expansion. Br. J. Haematol, 44:535-546, 1980.
10. Maier-Redelsperger, M., Noguchi, C.T., de Montalembert, M., Rodgers, G.P., Schlechter, A.N., Gourbil, A., Blanchard, D., Jais, J.P., Ducrocq, R., Peltier, J.Y., Cottat, M.C., Lacaille, F., Belloy, M., Elion, J., Labie, D., and Girot, R.: Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in Sickle Cell Children in the first two years of life: Parisian prospective study on Sickle Cell Disease. Blood, 84:3182-3188, 1994.
11. Thorpe, S.J. and Huehns, E.R.: A new approach for the antenatal diagnosis of β-thalassaemia: a double labelling immunofluorescence microscopy technique. Br. J. Haematol., 53:103-112, 1983.
12. Thorpe, S.J., Thein, S.L., Sampietro, M., Craig, I.E., Mahon, B., and Huehns, R.: Immunochemical estimation of haemoglobin types in red blood cells by FACS analysis. Br. J. Haematol., 87: 125-132, 1994.
13. Dover, G.J. and Boyer, S.H.: Fetal hemoglobin containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma and beta globin gene expression in normal subjects and in those with high fetal hemoglobin production. Blood, 69:1109-1113, 1987.
14. Horiuchi, K., Osterhout, M.L., Kamma, H., Bekoe, N.A., and Hirokawa, K.J.: Estimation of fetal hemoglobin levels in individual red cells via fluorescence image cytometry. Cytometry, 20:261-267, 1995.
15. Franco, R.S., Barker-Gear, R., Miller, M.A., Williams, S., Joiner, C.H., and Rucknagel, D.L.: Fetal hemoglobin and potassium in isolated transferrin receptor-positive dense sickle reticulocytes. Blood, 84:2013-2020, 1994.
16. Osterhout, M.L., Ohene-Frempong, K., and Horiuchi, K.: Identification ofF reticulocytes by two-stage fluorescence image cytometry. Blood, 86:485a(Suppl. 1), 1995.
17. Horiuchi, K., Osterhout, M.L., and Ohene-Frempong, K.: Survival of F reticulocytes in Sickle Cell Disease. Blood, 86:136a(Suppl. 1), 1995.
18. Dover, G.J. and Boyer, S.H.: The cellular distribution of fetal hemoglobin: normal adults and hemoglobinopathies. In: Human Hemoglobins and Hemoglobinopathies; a Review to 1981, edited by R.G. Schneider, S. Charache, and W.A. Schroeder, Texas Reports on Biology and Medicine, Vol. 40, pages 43-54, The University of Texas Medical Branch, Galveston, TX, USA, 1981.
19. Maier-Redelsperger, M., de Montalembert, M., Flahault, A., Neonato, M.G., Ducrocq, R., Masson, M.P., Girot, R., and Elion, J.: Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients. Blood, 91:4472-4479, 1998.