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采用局部胸部照射,随后用含胞壁酰三肽的脂质体进行全身巨噬细胞激活,来治疗实验性肺转移。

Treatment of experimental lung metastasis with local thoracic irradiation followed by systemic macrophage activation with liposomes containing muramyl tripeptide.

作者信息

Saiki I, Milas L, Hunter N, Fidler I J

出版信息

Cancer Res. 1986 Oct;46(10):4966-70.

PMID:3756858
Abstract

The purpose of these studies was to determine whether the combination of a low-dose local thoracic irradiation (LTI) followed by systemic activation of macrophages with liposomes containing muramyl tripeptide phosphatidylethanolamine (MTP-PE) would significantly decrease established experimental fibrosarcoma lung metastases. Male C3Hf/Kam mice were given i.v. injections of 1 X 10(5) fibrosarcoma cells. Five days later, groups of mice were treated with saline, with 8 Gy LTI, or with liposomes containing MTP-PE or first with 8 Gy LTI and followed by multiple i.v. injections of liposomes containing MTP-PE. Most of the mice in the groups treated with liposomes died by day 42 of the experiment. In contrast, 60% of the mice treated with the combination of LTI and liposomes containing MTP-PE were alive by day 140 of the study. These mice were killed and were found to be free of tumors. Control studies demonstrated that liposomes administered i.v. to mice given LTI were trapped in the capillary bed of the lungs and activated the tumoricidal properties of lung macrophages. We conclude that, in this combination, low-dose LTI, which can lead to both tumor cell death and inflammatory changes in the lung capillaries, could precede i.v. administration of liposomes containing MTP-PE. This combination of treatments can lead to destruction of tumor foci in the lung that cannot be achieved with either treatment alone.

摘要

这些研究的目的是确定低剂量局部胸部照射(LTI)后,再用含有胞壁酰三肽磷脂酰乙醇胺(MTP-PE)的脂质体进行巨噬细胞的全身激活,是否会显著减少已形成的实验性纤维肉瘤肺转移灶。给雄性C3Hf/Kam小鼠静脉注射1×10⁵个纤维肉瘤细胞。五天后,将小鼠分组,分别用生理盐水、8 Gy的LTI、含有MTP-PE的脂质体处理,或者先用8 Gy的LTI,随后多次静脉注射含有MTP-PE的脂质体。在实验的第42天,大多数接受脂质体处理的小鼠死亡。相比之下,在研究的第140天,60%接受LTI和含有MTP-PE脂质体联合处理的小鼠存活。这些小鼠被处死,发现没有肿瘤。对照研究表明,给接受LTI的小鼠静脉注射脂质体后,脂质体会被困在肺毛细血管床中,并激活肺巨噬细胞的杀肿瘤特性。我们得出结论,在这种联合治疗中,低剂量的LTI可导致肿瘤细胞死亡和肺毛细血管的炎症变化,可先于静脉注射含有MTP-PE的脂质体。这种联合治疗可导致肺内肿瘤病灶的破坏,而单独使用任何一种治疗方法都无法实现这一点。

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