Effects of a novel purine nucleoside phosphorylase inhibitor, BCX-34, on activation and proliferation of normal human lymphoid cells

被引:17
作者
Conry, RM
Bantia, S
Turner, HS
Barlow, DL
Allen, KO
LoBuglio, AF
Montgomery, JA
Walsh, GM
机构
[1] Univ Alabama Birmingham, Ctr Comprehens Canc, Birmingham, AL 35294 USA
[2] BioCryst Pharmaceut, Birmingham, AL 35244 USA
来源
IMMUNOPHARMACOLOGY | 1998年 / 40卷 / 01期
关键词
BCX-34; purine nucleoside phosphorylase; T-cell; IL-2; mixed lymphocyte reaction; OKT3; tetanus toroid;
D O I
10.1016/S0162-3109(98)00012-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The antiproliferative effect of BCX-34 was tested in normal human peripheral blood mononuclear cells (PBMCs) induced to proliferate with OKT3, tetanus toroid, the mixed lymphocyte reaction, or IL-2. In the case of OKT3, tetanus toroid, or the MLR the ICS(50)s ranged between 0.7 and 4 mu M. With IL-2, the IC50 was 14.6 mu M. In T-cells purified by resetting the IC50 with IL-2 was 0.62 mu M In CD4 or CD8 cells obtained by magnetic activated cell sorting the IC(50)s with IL-2 were 0.24 and 0.62 mu M, respectively. BCX-34 inhibition of proliferation in human PBMCs may not depend entirely upon the accumulation of intracellular dGTP because tetanus toroid-induced proliferation was inhibited in the absence of deoxyguanosine and was not reversed by deoxycytidine. BCX-34 did not inhibit IL-2 release from PBMCs and did not alter PBMC viability. The results of these studies show that BCX-34 is a potent inhibitor of normal human T-cell proliferation induced by antigenic or IL-2 stimulation. BCX-34 in normal human T-cells has a deoxyguanosine-independent mechanism to suppress in vitro proliferation. BCX-34 appears to have Little effect on T-cell viability. The data suggest that BCX-34 may be useful in the treatment of T-cell proliferative disorders. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
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页码:1 / 9
页数:9
相关论文
共 22 条
[1]   In vivo and in vitro pharmacologic activity of the purine nucleoside phosphorylase inhibitor BCX-34: The role of GTP and dGTP [J].
Bantia, S ;
Montgomery, JA ;
Johnson, HG ;
Walsh, GM .
IMMUNOPHARMACOLOGY, 1996, 35 (01) :53-63
[2]  
BENNETT LL, 1993, J PHARMACOL EXP THER, V266, P707
[3]   EVIDENCE FOR A PATHWAY INDEPENDENT FROM 2'-DEOXYGUANOSINE AND REVERSIBLE BY IL-2 BY WHICH PURINE NUCLEOSIDE PHOSPHORYLASE INHIBITORS BLOCK T-CELL PROLIFERATION [J].
BOEHNCKE, WH ;
GILBERTSEN, RB ;
HEMMER, J ;
STERRY, W .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1994, 39 (03) :327-332
[4]  
CATAPANO CV, 1995, MOL PHARMACOL, V47, P948
[5]   ALLOSTERIC REGULATION OF CALF THYMUS RIBONUCLEOSIDE DIPHOSPHATE REDUCTASE [J].
ERIKSSON, S ;
THELANDER, L ;
AKERMAN, M .
BIOCHEMISTRY, 1979, 18 (14) :2948-2952
[6]   COMPARATIVE INVITRO AND INVIVO ACTIVITIES OF 2 9-DEAZAGUANINE ANALOG INHIBITORS OF PURINE NUCLEOSIDE PHOSPHORYLASE, CI-972 AND PD-141955 [J].
GILBERTSEN, RB ;
JOSYULA, U ;
SIRCAR, JC ;
DONG, MK ;
WU, WS ;
WILBURN, DJ ;
CONROY, MC .
BIOCHEMICAL PHARMACOLOGY, 1992, 44 (05) :996-999
[7]   PRELIMINARY-REPORT ON 8-AMINO-9-(2-THIENYLMETHYL)GUANINE (PD 119,229), A NOVEL AND POTENT PURINE NUCLEOSIDE PHOSPHORYLASE INHIBITOR [J].
GILBERTSEN, RB ;
SCOTT, ME ;
DONG, MK ;
KOSSAREK, LM ;
BENNETT, MK ;
SCHRIER, DJ ;
SIRCAR, JC .
AGENTS AND ACTIONS, 1987, 21 (3-4) :272-274
[8]   ACTIVITIES OF 2 9-DEAZAGUANINE ANALOG INHIBITORS OF PURINE NUCLEOSIDE PHOSPHORYLASE, CI-972 AND PD-141955, IN-VITRO AND IN-VIVO [J].
GILBERTSEN, RB ;
DONG, MK ;
JOSYULA, U ;
SIRCAR, JC ;
WILBURN, DJ ;
CONROY, MC .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1993, 685 :248-251
[9]   LYMPHOCYTE-T ANTIGEN INTERACTIONS IN TRANSPLANT REJECTION [J].
KRENSKY, AM ;
WEISS, A ;
CRABTREE, G ;
DAVIS, MM ;
PARHAM, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (08) :510-517
[10]   THE T-CELL RECEPTOR REPERTOIRE AND AUTOIMMUNE-DISEASES [J].
KUMAR, V ;
KONO, DH ;
URBAN, JL ;
HOOD, L .
ANNUAL REVIEW OF IMMUNOLOGY, 1989, 7 :657-682