Clonality of isolated eosinophils in the hypereosinophilic syndrome

Blood

Volumn 93, Issue 5, 1999, Pages 1651-1657

  Chang, Hsiao Wen ^b   Leong, Kah Hoo ^b   Koh, Dow Rhoon ^b   Lee, Szu Hee ^a  

^a NATIONAL UNIVERSITY HOSPITAL   (Singapore)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR; CORTICOSTEROID; DNA; TRINUCLEOTIDE;

ADULT; AGED; ARTICLE; AUTOFLUORESCENCE; CHURG STRAUSS SYNDROME; EOSINOPHIL; FEMALE; FLOW CYTOMETRY; GENE; HUMAN; HUMAN CELL; HYPEREOSINOPHILIC SYNDROME; METHYLATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT; X CHROMOSOME INACTIVATION;

EID: 0033104707     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v93.5.1651     Document Type: Article

References (32)

1. Fauci AS Harley JB, Roberts WC, Ferrans VJ, Gralnick HR, Bjornson BH: NIH Conference. The idiopathic hypereosinophilic syndrome. Clinical, pathophysiologic, and therapeutic considerations. Ann Intern Med 97:78, 1987
2. Weller PF, Bubley GJ: The idiopathic hypereosinophilic syndrome. Blood 83:2759, 1994
3. Chusid MJ, Dale DC, West BC, Wolff SM: The hypereosinophilic syndrome: Analysis of fourteen cases with review of the literature. Medicine (Baltimore) 54:1, 1975
4. Lefebvre C, Bletry O, Degoulet P, Guillevin L, Bentata-Pesyre M, Le Thi HD, Godeau P: Facteurs pronostiques du syndrome hyperéosinophilique. Etude de 40 observations. Ann Med Interne (Paris) 140:253, 1989
5. Schooley RT, Flaum MA, Gralnick HR, Fauci AS: A clinicopathologic correlation of the idiopathic hypereosinophilic syndrome. II. Clinical manifestations. Blood 58:1021, 1981
6. Brito-Babapulle F: Clonal eosinophilic disorders and the hypereosinophilic syndrome. Blood Rev 11:129, 1997
7. Vogelstein B, Fearon ER, Hamilton SR, Preisinger AC, Willard HF, Michelson AM, Riggs AD, Orkin SH: Clonal analysis using recombinant DNA probes from the X-chromosome. Cancer Res 47: 4806, 1987
8. Boyd Y, Fraser NJ: Methylation patterns at the hypervariable X-chromosome locus DXS255 (M27β): Correlation with X-inactivation status. Genomics 7:182, 1990
9. Allen CR, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW: Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen receptor gene correlates with X-chromosome inactivation. Am J Hum Genet 51:1229, 1992
10. Gale RE, Wainscoat JS: Clonal analysis using X-linked DNA polymorphisms. Br J Haematol 85:2, 1993
11. Lyon MF: X-chromosome inactivation and developmental patterns in mammals. Biol Rev Camb Philos Soc 47:1, 1972
12. Riggs AD: X-inactivation, differentiation and DNA-methylation. Cytogenet Cell Genet 14:9, 1975
13. Martin GR, Epstein CJ, Travis B, Tucker G, Yatziv S, Martin DW Jr, Clift C, Cohen S: X-chromosome inactivation during differentiation of female teratocarcinoma stem cells in vitro. Nature 271:329, 1978
14. Lyon MF: X-chromosome inactivation and the location and expression of X-linked genes. Am J Hum Genet 42:8, 1988
15. Busque L, Gilliland G: Clonal evolution in acute myeloid leukemia. Blood 82:337, 1993
16. Luppi M, Marasca R, Morselli M, Barozzi P, Torelli G: Clonal nature of the hypereosinophilic syndrome. Blood 84:349, 1994
17. Gale RE, Mein CA, Linch DC: Quantification of X-chromosome inactivation patterns in haematological samples using the DNA PCR-based HUMARA assay. Leukemia 10:362, 1996
18. Weil GJ, Chused TM: Eosinophil autofluorescence and its use in isolation and analysis of human eosinophils using flow microfluorometry. Blood 57:1099, 1981
19. Mayeno AN, Hamann KJ, Gleich GJ: Granule-associated flavin adenine dinucleotide (FAD) is responsible for eosinophil autofluorescence. J Leukoc Biol 51:172, 1992
20. Maniatis T, Fritsch EF, Sambrook J: Molecular cloning: A Laboratory Manual. Cold Spring Harbor, NY, Cold Spring Harbor Laboratory, 1988
21. Anan K, Ito M, Misawa M, Ohe Y, Kai S, Kohsaki M: Clonal analysis of peripheral blood and haemopoietic colonies in patients with aplastic anaemia and refractory anaemia using polymorphic short tandem repeat on the HUMARA gene. Br J Haematol 89:839, 1995
22. Gilliland DG, Blanchard KL, Levy J, Perrin S, Bunn HF: Clonality in myeloproliferative disorders: Analysis by the polymerase chain reaction. Proc Natl Acad Sci USA 88:6848, 1991
23. Churg J, Strauss L: Allergic granulomatosis, allergic angiitis and periarteritis nodosa. Am J Pathol 27:277, 1951
24. Masi AT, Hunder GG, Lie JT, Michael BA, Bloch DA, Arend WP, Calabrese LH, Edworthy SM, Fauci AS, Leavitt RY, Lightfoot RWJ, McShane DJ, Mills JA, Stevens MB, Wallace SL, Zvaifler NJ: The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis). Arthritis Rheum 33:1094, 1990
25. Parillo JE, Lawley TJ, Frank MM, Kaplan AP, Fauci AS: Immunologic reactivity in the hypereosinophilic syndrome. J Allergy Clin Immunol 64:113, 1979
26. Parillo JE, Fauci AS, Wolff SM: Therapy of the hypereosinophilic syndrome. Ann Intern Med 89:167, 1978
27. Sanderson CJ: Interleukin 5, eosinophils and disease. Blood 79:3101, 1992
28. Cogan E, Schandené L, Crusiaux A, Cochaux P, Velu T, Goldman M: Clonal proliferation of type 2 helper T cells in a man with hypereosinophilic syndrome. N Engl J Med 330:535, 1994
29. Kitano K, Ichikawa N, Shimodaira S, Ito T, Ishida F, Kiyosawa K: Eosinophilia associated with clonal T-cell proliferation. Leuk Lymphoma 27:335, 1997
30. Spry CJF: Idiopathic hypereosinophilic syndrome, in Makino T, Fukuda S (eds): Eosinophils: Biological and Clinical Aspects. Boca Raton, FL, CRC, 1992, p 403
31. Weller PF, Goetze EJ: The regulatory and effector roles of eosinophils. Adv Immunol 27:339, 1979
32. Bain BJ: Eosinophilic leukaemias and the idiopathic hypereosinophilic syndrome. Br J Haematol 95:2, 1996