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根据免疫状态评估小鼠白血病化疗的疗效:重新审视化疗、肿瘤细胞杀伤与生存时间之间的相关性

Effectiveness of murine leukemia chemotherapy according to the immune state: reconsideration of correlations between chemotherapy, tumour cell killing, and survival time.

作者信息

Mathé G, Halle-Pannenko O, Bourut C

出版信息

Recent Results Cancer Res. 1977(62):9-12. doi: 10.1007/978-3-642-81174-6_3.

DOI:10.1007/978-3-642-81174-6_3
PMID:304590
Abstract

Cyclophosphamide (CPM) chemotherapy (134 mg/kg) of L1210 leukemia is less efficient in mice previously immunodepressed by antithymocyte serum (ATS) than in non-ATS pretreated mice. On the other hand, administration of a higher dose of CPM (403 mg/kg), which kills a greater number of leukemic cells but induces an immunodepression, according to the skin graft test, results in a shorter survival time than does the administration of a lower dose of CPM (134 mg/kg), capable of killing fewer leukemic cells but not inducing such an immunodepression. Thus, it appears that: (1) the antileukemic effect of the same dose of a chemotherapeutic drug is less efficient in immunodepressed than in nonimmunodepressed hosts, and (2) calculation of the number of neoplastic cells killed by a given chemotherapy by extrapolation from the survival time may lead to erroneous conclusions.

摘要

环磷酰胺(CPM)对L1210白血病的化疗(134毫克/千克),在先前用抗胸腺细胞血清(ATS)免疫抑制的小鼠中,其效率低于未用ATS预处理的小鼠。另一方面,根据皮肤移植试验,给予更高剂量的CPM(403毫克/千克),虽然能杀死更多的白血病细胞,但会诱导免疫抑制,与给予较低剂量的CPM(134毫克/千克)相比,其存活时间更短。较低剂量的CPM能杀死较少的白血病细胞,但不会诱导这种免疫抑制。因此,似乎:(1)相同剂量的化疗药物的抗白血病作用在免疫抑制宿主中比在非免疫抑制宿主中效率更低;(2)通过从存活时间外推来计算给定化疗杀死的肿瘤细胞数量可能会得出错误的结论。

相似文献

1
Effectiveness of murine leukemia chemotherapy according to the immune state: reconsideration of correlations between chemotherapy, tumour cell killing, and survival time.根据免疫状态评估小鼠白血病化疗的疗效:重新审视化疗、肿瘤细胞杀伤与生存时间之间的相关性
Recent Results Cancer Res. 1977(62):9-12. doi: 10.1007/978-3-642-81174-6_3.
2
[Immune manipulation of BCG administered before or after cyclophosphamide for chemo-immunotherapy of L1210 leukemia].[环磷酰胺治疗L1210白血病的化学免疫疗法中,卡介苗在其之前或之后给药的免疫调控]
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Active immunotherapy in spontaneous leukemia of AkR mice.对AkR小鼠自发性白血病的主动免疫疗法。
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Combined antitumor effect of cyclophosphamide and bromodeoxyuridine in BDF1 mice bearing L1210 ascites tumors.环磷酰胺与溴脱氧尿苷对BDF1小鼠L1210腹水瘤的联合抗肿瘤作用。
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Predictive values of the in vivo diffusion chamber for cyclophosphamide treatment of L1210 murine leukemia.体内扩散室对环磷酰胺治疗L1210小鼠白血病的预测价值。
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引用本文的文献

1
Effect of cisplatin upon expression of in vivo immune tumor resistance.顺铂对体内免疫肿瘤抗性表达的影响。
Cancer Immunol Immunother. 1993;36(1):18-24. doi: 10.1007/BF01789126.
2
Transforming growth factor-beta-mediated down-regulation of antitumor cytotoxicity of spleen cells from MOPC-315 tumor-bearing mice engaged in tumor eradication following low-dose melphalan therapy.转化生长因子-β介导荷MOPC-315肿瘤小鼠脾细胞抗肿瘤细胞毒性的下调,这些脾细胞在小剂量美法仑治疗后参与肿瘤清除。
Cancer Immunol Immunother. 1994 Apr;38(4):215-24. doi: 10.1007/BF01533512.
3
Interference of anti-tumor and immunosuppressive effects of cyclophosphamide in tumor-bearing rats. Analysis of factors determining resistance or susceptibility to a subsequent tumor challenge.
环磷酰胺对荷瘤大鼠抗肿瘤及免疫抑制作用的干扰。对决定对后续肿瘤攻击产生抗性或易感性的因素的分析。
Cancer Immunol Immunother. 1982;14(1):36-40. doi: 10.1007/BF00199430.
4
Increase in the effectiveness of melphalan therapy with progression of MOPC-315 plasmacytoma tumor growth.随着MOPC - 315浆细胞瘤肿瘤生长进展,美法仑治疗效果增强。
Cancer Immunol Immunother. 1983;15(2):101-7. doi: 10.1007/BF00199699.
5
Melphalan-induced enhancement of tumor cell immunostimulatory capacity as a mechanism for the appearance of potent antitumor immunity in the spleen of mice bearing a large metastatic MOPC-315 tumor.美法仑诱导肿瘤细胞免疫刺激能力增强,作为荷大转移灶MOPC - 315肿瘤小鼠脾脏中出现强效抗肿瘤免疫的一种机制。
Cancer Immunol Immunother. 1985;20(1):61-8. doi: 10.1007/BF00199775.
6
Some characteristics of the in vivo antitumor immunity exhibited by mice cured of a large MOPC-315 tumor by a low dose of melphalan.低剂量美法仑治愈大型MOPC - 315肿瘤的小鼠所表现出的体内抗肿瘤免疫的一些特征。
Cancer Immunol Immunother. 1987;25(3):215-24. doi: 10.1007/BF00199150.
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Cytocidal and toxic effect of various cytostatic drugs on three ascites tumors of the mouse.多种细胞抑制剂对小鼠三种腹水瘤的杀细胞及毒性作用。
J Cancer Res Clin Oncol. 1987;113(3):216-22. doi: 10.1007/BF00396376.
8
Specificity of the generation and expression of enhanced anti-plasmacytoma immunity by spleen cells from melphalan-treated MOPC-315 tumor bearers.美法仑处理的MOPC - 315荷瘤小鼠脾脏细胞产生和表达增强的抗浆细胞瘤免疫的特异性
Cancer Immunol Immunother. 1986;23(1):11-9. doi: 10.1007/BF00205549.
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In vivo resistance of secondary antitumor immune response to cyclophosphamide: effects on T cell subsets.环磷酰胺对继发性抗肿瘤免疫反应的体内抗性:对T细胞亚群的影响
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10
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