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1
[Study of immunosuppressive mechanism of deoxymethylspergualin in vitro].
Nihon Hinyokika Gakkai Zasshi. 1993 Jul;84(7):1301-7. doi: 10.5980/jpnjurol1989.84.1301.
2
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3
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4
In vitro immunosuppressive effect: a comparative study between deoxymethylspergualin and cyclosporin A, on human lymphocyte responses.体外免疫抑制作用:去氧甲基司帕沙星与环孢素A对人淋巴细胞反应的比较研究。
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5
The in vitro immunosuppressive effect of deoxymethylspergualin in man as compared with FK506 and cyclosporine.
Transplantation. 1992 Apr;53(4):914-8. doi: 10.1097/00007890-199204000-00037.
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Mechanism of action of 15-deoxyspergualin. I. Suppressive effect on the induction of alloreactive secondary cytotoxic T lymphocytes in vivo and in vitro.15-脱氧精胍菌素的作用机制。I. 对体内和体外同种异体反应性继发性细胞毒性T淋巴细胞诱导的抑制作用。
Immunology. 1989 Sep;68(1):66-71.
7
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J Antibiot (Tokyo). 1995 Mar;48(3):243-7. doi: 10.7164/antibiotics.48.243.
8
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9
A comparison of the sensitivity of pig and human peripheral blood mononuclear cells to the antiproliferative effects of traditional and newer immunosuppressive agents.猪和人外周血单个核细胞对传统及新型免疫抑制剂抗增殖作用的敏感性比较。
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10
Immunosuppressant deoxyspergualin induces apoptotic cell death in dividing cells.免疫抑制剂脱氧精胍菌素可诱导分裂细胞发生凋亡性细胞死亡。
Immunology. 1998 Nov;95(3):370-6. doi: 10.1046/j.1365-2567.1998.00606.x.

[Study of immunosuppressive mechanism of deoxymethylspergualin in vitro].

作者信息

Uemura T

机构信息

Department of Urology, Kinki University School of Medicine.

出版信息

Nihon Hinyokika Gakkai Zasshi. 1993 Jul;84(7):1301-7. doi: 10.5980/jpnjurol1989.84.1301.

DOI:10.5980/jpnjurol1989.84.1301
PMID:8355445
Abstract

Mechanism of action of Deoxyspergualin (DSG) in vitro has not been clarified, because it is unstable in solution. I studied its mechanism in vitro using Deoxymethylspergulin (MeDSG) that is stable in solution. Action of MeDSG was studied using human lymphocyte and a human T cell clone which was established in our laboratory. MeDSG showed dose dependent inhibition of blastogenesis in MLR. MeDSG inhibited the response by about 50% at the concentration of 10 micrograms/ml. It is a very interesting point that MeDSG added at 3 days later suppressed MLR. But MeDSG did not suppress MLR added at 4 days later or 2nd MLR. MeDSG did not have effects on the production of IL-1, IL-2 and the expression of IL-2 receptor on stimulated lymphocyte by mitogen. But MeDSG suppressed IFN-gamma production induced stimulation of alloantigen at only concentration of 1 microgram/ml. MeDSG did not suppress proliferation of helper T cell clone. On the other hand, CsA suppressed IL-2 receptor expression and proliferation of helper T cell clone. These results showed MeDSG act on relatively late phase of immunoreaction. From in vitro results, when we use DSG for clinical acute rejection, it is more appropriate to use DSG and Methylprednisolone at the same time to get early recovery.

摘要