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用在人类肿瘤中表达的合成九肽进行疫苗接种可预防同基因大鼠的结直肠癌肝转移。

Vaccination with a synthetic nonapeptide expressed in human tumors prevents colorectal cancer liver metastases in syngeneic rats.

作者信息

Sinibaldi Vallebona Paola, Rasi Guido, Pierimarchi Pasquale, Bernard Paola, Guarino Enrico, Guadagni Fiorella, Garaci Enrico

机构信息

Department of Experimental Medicine and Biochemical Sciences, University of Rome Tor Vergata, Rome, Italy.

出版信息

Int J Cancer. 2004 May 20;110(1):70-5. doi: 10.1002/ijc.20063.

Abstract

In previous studies, the antigen CSH-275 (RTNKEASIC) was found expressed in tissue specimens from colorectal cancer but not in normal colonic mucosa. It was also naturally expressed in the DHD-K12 experimental colorectal cancer in BDIX rats. In this study, we describe the effect of vaccination with the synthetic nonapeptide CSH-275 in preventing tumor growth in a model closely mimicking the clinical situation of liver metastases, after surgical resection of primary colorectal cancer. A vaccination protocol using CSH-275, conjugated with complete or incomplete Freund's adjuvant, was carried out to determine the effect in preventing the progression of liver metastases induced by DHD-K12 cells injected in the splenic vein (preventive vaccine). An additional vaccination procedure was carried out to determine the effect on s.c. tumor growth (therapeutic vaccine). A significant improvement in survival along with the prevention of liver metastases formation and reduced growth of s.c. tumor were observed. CSH-275 vaccination resulted in a significant increase in CTL activity against autologous DHD-K12 cells in DHD-K12 tumor-bearing rats and the generation of a CTL response against DHD-K12 cells in DHD-K12 naive rats. Vaccination also induced massive infiltration of CD8(+) cells in tumor. These results demonstrate that CSH-275 is a new molecular target for colorectal cancer immunotherapy; it is also an excellent candidate for preclinical studies because it is naturally expressed on tumors in a fully competent syngeneic animal, which reproduces the clinical pattern of cancer progression.

摘要

在先前的研究中,发现抗原CSH-275(RTNKEASIC)在结直肠癌组织标本中表达,但在正常结肠黏膜中不表达。它也在BDIX大鼠的DHD-K12实验性结直肠癌中自然表达。在本研究中,我们描述了用合成九肽CSH-275进行疫苗接种在模拟原发性结直肠癌手术切除后肝转移临床情况的模型中预防肿瘤生长的效果。采用与完全或不完全弗氏佐剂偶联的CSH-275进行疫苗接种方案,以确定预防经脾静脉注射DHD-K12细胞诱导的肝转移进展的效果(预防性疫苗)。还进行了额外的疫苗接种程序以确定对皮下肿瘤生长的影响(治疗性疫苗)。观察到存活率显著提高,同时预防了肝转移的形成并减少了皮下肿瘤的生长。CSH-275疫苗接种导致DHD-K12荷瘤大鼠中针对自体DHD-K12细胞的CTL活性显著增加,并在DHD-K12未致敏大鼠中产生针对DHD-K12细胞的CTL反应。疫苗接种还诱导了肿瘤中CD8(+)细胞的大量浸润。这些结果表明,CSH-275是结直肠癌免疫治疗的新分子靶点;它也是临床前研究的优秀候选物,因为它在完全同源的动物的肿瘤上自然表达,再现了癌症进展的临床模式。

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