PHARMACOLOGICAL PURGING OF MALIGNANT T-CELLS FROM HUMAN BONE-MARROW USING 9-BETA-D-ARABINOFURANOSYLGUANINE

被引:22
作者
HEBERT, ME
GREENBERG, ML
CHAFFEE, S
GRAVATT, L
HERSHFIELD, MS
ELION, GB
KURTZBERG, J
机构
[1] DUKE UNIV,MED CTR,DEPT PEDIAT,DIV HEMATOL & ONCOL,BOX 2916,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT MED,DIV RHEUMATOL & IMMUNOL,DURHAM,NC 27710
关键词
D O I
10.1097/00007890-199110000-00011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Arabinosylguanine (araG) is a nucleoside analog that is rapidly converted by cells of the T lymphoid lineage to its corresponding arabinosylguanine nucleotide triphosphate, resulting in inhibition of DNA synthesis and selective in vitro toxicity to T lymphoblastoid cell lines as well as to freshly isolated leukemia cells from patients with T cell acute lymphoblastic leukemia. In this report, we demonstrate that araG is an effective agent to use for chemoseparation of malignant T lymphoblasts from human bone marrow. When freshly isolated human T leukemia cells or T lymphoblastoid cells were treated with 100-mu-M araG for 18 hr, up to 6 logs of clonogenic T cells could be eliminated without appreciable toxicity to the normal myeloid, erythroid, and megakaryocytoid clonal progenitor cells. We discuss the use of this agent in ex vivo elimination of residual malignant T cells from marrow of patients requiring myeloablative chemotherapy with autologous bone marrow rescue.
引用
收藏
页码:634 / 640
页数:7
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