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The effects of STI571 on antigen presentation of dendritic cells generated from patients with chronic myelogenous leukemia
被引:33
|作者:
Sato, N
Narita, M
Takahashi, M
Yagisawa, K
Liu, A
Abe, T
Nikkuni, K
Furukawa, T
Toba, K
Aizawa, Y
机构:
[1] Niigata Univ, Sch Med, Dept Internal Med 1, Niigata 9518520, Japan
[2] Niigata Univ, Sch Med, Sch Hlth Sci, Niigata 9518520, Japan
[3] Niigata Univ, Sch Med, Div Bone Marrow Transplantat, Niigata 9518520, Japan
关键词:
STI571;
dendritic cells;
chronic myelogenous leukemia;
surface phenotypes;
antigen presentation;
D O I:
10.1002/hon.705
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Chronic myelogenous leukemia is caused by the acquisition of the reciprocal (9;22)(q34;q11) chromosomal translocation in hematopoietic stem cells. The fusion protein showed higher and aberrant tyrosine kinase activity. The inhibition of the tyrosine kinase activity of the protein represents a specific therapeutic strategy for bcr/ablexpressing leukemias. STI571 is a compound of the 2-phenylaminopyrimidine class that selectively inhibits the tyrosine kinase activity of the AN protein tyrosine kinase. In this study. we evaluated the effects of ST1571 on antigen presentation of dendritic cells generated from the patients with CML. The data showed that by the addition of ST1571 the dendritic cells derived from CML clone showed an increased expression of CD1a, CD83, CD80 and CD86 by flow cytometry analysis and showed more intense abilities of allogeneic antigen presentation by mixed leukocyte culture, compared with the control cells without ST1571. Our results suggested that ST1571 not only has a direct cytotoxic effect on bcr-abl gene rearranged cells but also an indirect effect associated with increased anti-leukemic immunological function due to an intensified antigen presentation. Copyright (C) 2003 John Wiley Sons, Ltd.
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页码:67 / 75
页数:9
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