EXPRESSION OF HEMATOPOIETIC PROGENITOR-CELL ASSOCIATED ANTIGEN-CD34 IN CHRONIC MYELOID-LEUKEMIA

被引:17
作者
BANAVALI, S
SILVESTRI, F
HULETTE, B
HURTUBISE, P
SRIVASTAVA, A
CIVIN, CI
PREISLER, HD
机构
[1] UNIV CINCINNATI, MED CTR, BARRETT CANC CTR, 234 GOODMAN ST, CINCINNATI, OH 45267 USA
[2] UNIV CINCINNATI, DIV DIAGNOST IMMUNOL, CINCINNATI, OH 45221 USA
[3] UNIV CINCINNATI, DEPT PATHOL, CINCINNATI, OH 45221 USA
[4] JOHNS HOPKINS UNIV HOSP, CTR ONCOL, DIV PEDIAT ONCOL, BALTIMORE, MD 21205 USA
[5] UNIV UDINE POLICLIN, CATTEDRA EMATOL, UDINE, ITALY
关键词
CHRONIC MYELOID LEUKEMIA; HEMATOPOIETIC PROGENITOR CELLS; CD34; ANTIGEN; MONOCLONAL ANTIBODY; IMMUNOPHENOTYPE;
D O I
10.1016/0145-2126(91)90029-S
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The expression of progenitor cell associated antigen CD34 was investigated in cells from 28 patients with chronic myeloid leukemia (CML). The CD34 positivity varied from 0-26% in patients with chronic phases CML (n = 17); from 6-64% in patients with accelerated phase CML (n = 4); and from 27-97% in the patients with blastic crisis of CML (n = 8). The difference in CD34 positivity between chronic (mean 10.1 +/- 2.3%), accelerated (37.7 +/- 13.3%) and blastic (58.0 +/- 7.3%) phases of CML is statistically significant (p < 0.05), however, the number of patients studied, especially in accelerated and blastic phases is very small. There was no difference in the CD34 positivity of the cells in the peripheral blood and in the bone marrow. CD34 positivity was higher in patients with chronic phase CML at diagnosis (untreated patients) than in those who were studied during treatment. The possible importance of serially studying CD34 positivity in patients with CML is discussed in the paper.
引用
收藏
页码:603 / 608
页数:6
相关论文
共 23 条
[11]  
LEONG SS, 1979, CANCER RES, V39, P2704
[12]  
LU L, 1987, Journal of Immunology, V139, P1823
[13]   CHARACTERIZATION OF MYELOID LEUKEMIAS WITH MONOCLONAL ANTIBODIES-3C5 AND ANTIBODIES-MY9 [J].
MATUTES, E ;
RODRIGUEZ, B ;
POLLI, N ;
DECASTRO, JT ;
PARREIRA, A ;
ANDREWS, C ;
GRIFFIN, JD ;
TINDLE, RW ;
CATOVSKY, D .
HEMATOLOGICAL ONCOLOGY, 1985, 3 (03) :179-186
[14]  
RYAN D, 1986, BLOOD, V68, P417
[15]   ATTEMPTED PREVENTION OF BLAST CRISIS IN CHRONIC MYELOID-LEUKEMIA BY THE USE OF PULSED DOSES OF CYTOSINE-ARABINOSIDE AND CIS-CHLORONITROSUREA DURING THE COURSE OF BUSULFAN-MAINTAINED REMISSION [J].
SILVER, RT ;
MICK, R ;
DEGNAN, TJ ;
HOLLAND, JF ;
CAVELLI, F .
CANCER INVESTIGATION, 1988, 6 (03) :255-262
[16]   A SIMPLE RELIABLE PROCEDURE FOR OBTAINING METAPHASES FROM HUMAN-LEUKEMIC BONE-MARROW ASPIRATES SUITABLE FOR GIEMSA-BANDING [J].
SRIVASTAVA, AK ;
SMITH, RD .
IN VITRO-JOURNAL OF THE TISSUE CULTURE ASSOCIATION, 1980, 16 (02) :109-112
[17]  
STRAUSS LC, 1986, EXP HEMATOL, V14, P878
[18]  
STRAUSS LC, 1984, BLOOD, V64, pA117
[19]  
STRIFE A, 1988, SEMIN HEMATOL, V25, P1
[20]   A NOVEL MONOCLONAL-ANTIBODY BI-3C5 RECOGNIZES MYELOBLASTS AND NON-B NON-T LYMPHOBLASTS IN ACUTE LEUKEMIAS AND CGL BLAST CRISES, AND REACTS WITH IMMATURE CELLS IN NORMAL BONE-MARROW [J].
TINDLE, RW ;
NICHOLS, RAB ;
LI, C ;
CAMPANA, D ;
CATOVSKY, D ;
BIRNIE, GD .
LEUKEMIA RESEARCH, 1985, 9 (01) :1-9