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耐受性对小鼠肿瘤坏死因子抗肿瘤疗效的影响。

Impact of tolerance on antitumor efficacy of tumor necrosis factor in mice.

作者信息

Fraker D L, Sheppard B C, Norton J A

机构信息

Surgical Metabolism Section, National Cancer Institute, NIH, Bethesda, Maryland 20892.

出版信息

Cancer Res. 1990 Apr 15;50(8):2261-7.

PMID:2317813
Abstract

Repetitive sublethal doses of tumor necrosis factor (TNF) can induce tolerance or tachyphylaxis to the toxic effects of TNF. Because tumor-bearing (TB) mice are more sensitive to the toxic effects of TNF, this study investigates whether similar tolerance occurs in TB mice and whether it affects the antitumor response of TNF. Nontumor-bearing C3H/Hen mice were treated with twice daily i.p. sublethal escalating doses of human recombinant TNF (2, 2, 3, 3, 4, and 4 micrograms i.p. every 12 h for 6 days) and were challenged 2 days later with a lethal i.v. dose (40 micrograms) of TNF. TNF-pretreated mice had 100% survival as compared to 0% survival in control mice previously treated with saline (P less than 0.01). Tumor-bearing C57BL/6 mice bearing an MCA-106 or MCA-102 sarcoma were treated with an identical TNF-tolerizing regimen (2, 2, 3, 3, 4, and 4 micrograms i.p. every 12 h for 6 days) beginning 3 days following tumor inoculation and were similarly more resistant to a subsequent 100% lethal i.v. treatment dose of TNF than control TB mice. A significantly greater percentage of TNF-pretreated mice bearing the MCA-106 sarcoma survived treatment doses of 8, 12, and 16 micrograms of TNF i.v. than control TB mice. Similarly, a significantly greater percentage of TNF-pretreated mice bearing the MCA-102 sarcoma survived treatment doses of 6 and 9 micrograms of TNF i.v. than control TB mice. However, the ability to administer higher doses of TNF i.v. to TNF-pretreated TB mice did not improve therapeutic efficacy. In mice bearing the MCA-106 tumor the most efficacious treatment responses were seen in animals that were previously naive to TNF, and treatment toxicity (lethality) correlated directly with antitumor efficacy such that larger treatment doses of TNF in tolerant mice resulted in similar antitumor effects as smaller treatment doses in control TB mice. In mice bearing the MCA-102 tumor, equitoxic treatment doses of TNF produced similar antitumor effects in both control and tolerant TB mice. There were no differences in cure rate for TNF-tolerant or control TB mice bearing either tumor. The results suggest that TNF tolerance occurs in TB mice and reduces the toxicity as well as the therapeutic efficacy of TNF.

摘要

重复给予亚致死剂量的肿瘤坏死因子(TNF)可诱导对TNF毒性作用的耐受性或快速耐受。由于荷瘤(TB)小鼠对TNF的毒性作用更敏感,本研究调查了TB小鼠是否会出现类似的耐受性,以及这种耐受性是否会影响TNF的抗肿瘤反应。对无瘤的C3H/Hen小鼠每天腹腔注射两次亚致死递增剂量的人重组TNF(每12小时腹腔注射2、2、3、3、4和4微克,共6天),并在2天后静脉注射致死剂量(40微克)的TNF进行攻击。与先前用生理盐水处理的对照小鼠0%的存活率相比,经TNF预处理的小鼠存活率为100%(P<0.01)。接种肿瘤3天后,对携带MCA - 106或MCA - 102肉瘤的荷瘤C57BL/6小鼠采用相同的TNF耐受方案(每12小时腹腔注射2、2、3、3、4和4微克,共6天)进行处理,与对照TB小鼠相比,它们对随后100%致死剂量的静脉注射TNF同样更具抗性。携带MCA - 106肉瘤的经TNF预处理的小鼠在静脉注射8、12和16微克TNF治疗剂量后的存活百分比显著高于对照TB小鼠。同样,携带MCA - 102肉瘤的经TNF预处理的小鼠在静脉注射6和9微克TNF治疗剂量后的存活百分比显著高于对照TB小鼠。然而,对经TNF预处理的TB小鼠给予更高剂量静脉注射TNF的能力并未提高治疗效果。在携带MCA - 106肿瘤的小鼠中,对TNF既往未接触过的动物治疗反应最为有效,治疗毒性(致死率)与抗肿瘤疗效直接相关,因此耐受小鼠中较大剂量的TNF治疗产生的抗肿瘤效果与对照TB小鼠中较小剂量的治疗效果相似。在携带MCA - 102肿瘤的小鼠中,同等毒性剂量的TNF在对照和耐受的TB小鼠中产生相似的抗肿瘤效果。携带这两种肿瘤的TNF耐受或对照TB小鼠的治愈率没有差异。结果表明,TB小鼠中会出现TNF耐受性,这会降低TNF的毒性以及治疗效果。

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