Quality of IL-3 and G-CSF-mobilized peripheral blood stem cells in patients with early chronic phase CML

被引:15
作者
Heinzinger, M
Waller, CF
Rosenstiel, A
Scheid, S
Burger, KJ
Lange, W
机构
[1] Univ Freiburg, Med Ctr, Dept Hematol Oncol, D-79106 Freiburg, Germany
[2] Firma Sandoz, Nurnberg, Germany
[3] Univ Freiburg, Dept Biol, D-79106 Freiburg, Germany
关键词
CML; bcr/abl; autologous transplantation; PBPC; rhIL-3; rhG-CSF;
D O I
10.1038/sj.leu.2400960
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Coexistence of Philadelphia chromosome (Ph)-negative, primitive hematopoietic progenitor cells with their malignant counterparts in chronic myelogenous leukemia (CML) has been reported. As most of the Ph-negative progenitor cells do not express the HLA-DR antigen, selection of them might be possible. Peripheral blood progenitor cells (PBPC) from eight early chronic phase (CML) patients were mobilized by ICE chemotherapy followed by simultaneous administration of recombinant human granulocyte colony-stimulating factor (rhG-CSF) and recombinant human interleukin 3 (rhlL-3). PBPCs were collected by leukapheresis in the early phase of hematopoietic recovery after chemotherapy, CD34 selected and cultured in vitro. The content of Ph chromosome-positive cells in leukapheresis products as well as after CD34 enrichment and after in vitro culture was analyzed by interphase fluorescence in situ hybridization (FISH) and RT-PCR. The percentage of Ph chromosome-positive PBPC was reduced after each purification step in almost all samples. A substantial number of PBPC samples were negative for the bcr/abl mRNA rearrangement as analyzed by RT-PCR. The present study demonstrates the feasibility of mobilizing Ph-negative PBPC during the early phase of hematopoietic recovery after ICE chemotherapy and simultaneous administration of rhlL-3 and rhG-CSF.
引用
收藏
页码:333 / 339
页数:7
相关论文
共 28 条
[1]  
BARNETT MJ, 1994, BLOOD, V84, P724
[2]  
BEDI A, 1993, BLOOD, V81, P2898
[3]   AUTOGRAFTING FOR PATIENTS WITH CHRONIC MYELOID-LEUKEMIA IN CHRONIC PHASE - PERIPHERAL-BLOOD STEM-CELLS MAY HAVE A FINITE-CAPACITY FOR MAINTAINING HEMATOPOIESIS [J].
BRITOBABAPULLE, F ;
BOWCOCK, SJ ;
MARCUS, RE ;
APPERLEY, J ;
THNG, KH ;
DOWDING, C ;
RASSOOL, F ;
GUO, AP ;
CATOVSKY, D ;
GALTON, DAG ;
MCCARTHY, D ;
GOLDMAN, JM .
BRITISH JOURNAL OF HAEMATOLOGY, 1989, 73 (01) :76-81
[4]   PERIPHERAL-BLOOD PROGENITOR CELLS MOBILIZED BY CHEMOTHERAPY PLUS GRANULOCYTE-COLONY-STIMULATING FACTOR ACCELERATE BOTH NEUTROPHIL AND PLATELET RECOVERY AFTER HIGH-DOSE VP16, IFOSFAMIDE AND CISPLATIN [J].
BRUGGER, W ;
BIRKEN, R ;
BERTZ, H ;
HECHT, T ;
PRESSLER, K ;
FRISCH, J ;
SCHULZ, G ;
MERTELSMANN, R ;
KANZ, L .
BRITISH JOURNAL OF HAEMATOLOGY, 1993, 84 (03) :402-407
[5]  
CARELLA AM, 1993, BONE MARROW TRANSPL, V12, P267
[6]   Mobilization and transplantation of Philadelphia-negative peripheral-blood progenitor cells early in chronic myelogenous leukemia [J].
Carella, AM ;
Cunningham, I ;
Lerma, E ;
Dejana, A ;
Benvenuto, F ;
Podesta, M ;
Celesti, L ;
Chimirri, F ;
Abate, M ;
Vassallo, F ;
Figari, O ;
Parodi, C ;
Sessarego, M ;
Valbonesi, M ;
Carlier, P ;
Prencipe, E ;
Gatti, AM ;
VanDenBerg, D ;
Hoffman, R ;
Frassoni, F .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (04) :1575-1582
[7]   INDUCTION OF CHRONIC MYELOGENOUS LEUKEMIA IN MICE BY THE P210BCR/ABL GENE OF THE PHILADELPHIA-CHROMOSOME [J].
DALEY, GQ ;
VANETTEN, RA ;
BALTIMORE, D .
SCIENCE, 1990, 247 (4944) :824-830
[8]   THE EFFICACY OF DIRECT, 24-HOUR CULTURE, AND MITOTIC SYNCHRONIZATION METHODS FOR CYTOGENETIC ANALYSIS OF BONE-MARROW IN NEOPLASTIC HEMATOLOGIC DISORDERS [J].
DEWALD, GW ;
BRODERICK, DJ ;
TOM, WW ;
HAGSTROM, JE ;
PIERRE, RV .
CANCER GENETICS AND CYTOGENETICS, 1985, 18 (01) :1-10
[9]  
EAVES C, 1991, THERAPECTIC STRATEGI, P27
[10]   LOCALIZATION OF THE C-ABL ONCOGENE ADJACENT TO A TRANSLOCATION BREAK POINT IN CHRONIC MYELOCYTIC-LEUKEMIA [J].
HEISTERKAMP, N ;
STEPHENSON, JR ;
GROFFEN, J ;
HANSEN, PF ;
DEKLEIN, A ;
BARTRAM, CR ;
GROSVELD, G .
NATURE, 1983, 306 (5940) :239-242