The chemokine CCL21 protects normal marrow progenitors from Ara-C cytotoxicity

被引:3
作者
Hromas, R [1 ]
Cooper, S [1 ]
Broxmeyer, HE [1 ]
机构
[1] Indiana Univ, Med Ctr, Walther Oncol Ctr, Indianapolis, IN 46202 USA
关键词
chemokine; Ara-C; myelosuppression; leukemia; myeloid progenitors;
D O I
10.1007/s00280-002-0486-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Chemokines are a family of small proteins that regulate leukocyte infiltration into inflamed tissue and play key roles in the pathogenesis of many diseases. Some chemokines can also reversibly inhibit the proliferation of hematopoietic progenitors. We have previously found that the chemokine CCL21 (Exodus-2/SLC/6Ckine/TCA4) is a potent inhibitor of the: proliferation of normal hematopoietic progenitors. In this study we sought to determine whether this inhibition of proliferation could be therapeutically exploited by protecting normal marrow progenitors from the cytotoxicity of the S phase-active chemotherapeutic agent Ara-C. Methods: Untreated and CCL21-pretreated mice were given doses of Ara-C that are toxic to marrow myeloid progenitors. The recovery of these myeloid progenitors was analyzed by colony formation assays. Results: It was found that pretreatment with small doses of CCL21 prevented the death of normal murine marrow progenitors from the toxic effects of Ara-C. Conclusions: The chemokine CCL21 may be able to prevent Ara-C myelosuppression during acute leukemia induction chemotherapy, and thereby decrease morbidity and mortality of such therapy, and shorten hospital stays.
引用
收藏
页码:163 / 166
页数:4
相关论文
共 21 条
[1]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[2]   CC-CHEMOKINES IN ALLERGIC INFLAMMATION [J].
BAGGIOLINI, M ;
DAHINDEN, CA .
IMMUNOLOGY TODAY, 1994, 15 (03) :127-133
[3]   Effects of CC, CXC, C, and CX3C chemokines on proliferation of myeloid progenitor cells, and insights into SDF-1-induced chemotaxis of progenitors [J].
Broxmeyer, HE ;
Kim, CH ;
Cooper, SH ;
Hangoc, G ;
Hromas, R ;
Pelus, LM .
HEMATOPOIETIC STEM CELLS: BIOLOGY AND TRANSPLANTATION, 1999, 872 :142-163
[4]   Myeloid progenitor cell proliferation and mobilization effects of BB10010, a genetically engineered variant of human macrophage inflammatory protein-1α, in a phase I clinical trial in patients with relapsed/refractory breast cancer [J].
Broxmeyer, HE ;
Orazi, A ;
Hague, NL ;
Sledge, GW ;
Rasmussen, H ;
Gordon, MS .
BLOOD CELLS MOLECULES AND DISEASES, 1998, 24 (02) :14-30
[5]  
BROXMEYER HE, 1995, ANN HEMATOL, V71, P235, DOI 10.1007/s002770050112
[6]  
BROXMEYER HE, 1993, J IMMUNOL, V150, P3448
[7]  
Broxmeyer HE, 1999, CONT CANC RES, P263
[8]  
BROXMEYER HE, 1993, COLLOQ INSE, V229, P141
[9]   HIV-1 entry into CD4(+) cells is mediated by the chemokine receptor CC-CKR-5 [J].
Dragic, T ;
Litwin, V ;
Allaway, GP ;
Martin, SR ;
Huang, YX ;
Nagashima, KA ;
Cayanan, C ;
Maddon, PJ ;
Koup, RA ;
Moore, JP ;
Paxton, WA .
NATURE, 1996, 381 (6584) :667-673
[10]  
DUNLOP DJ, 1992, BLOOD, V79, P2221