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[使用源自肿瘤排斥抗原的肽进行癌症疫苗治疗]

[Cancer vaccine therapy using peptides derived from tumor-rejection antigens].

作者信息

Akiyoshi T

机构信息

Dept. of Surgery, Kyushu University, Beppu, Japan.

出版信息

Gan To Kagaku Ryoho. 1997 Mar;24(5):511-9.

PMID:9087280
Abstract

A number of genes coding tumor antigens have recently been isolated from human melanoma cell lines. The antigens encoded by these genes are recognized by autologous cytotoxic T lymphocytes (CTL) in the context of HLA class I molecules, and the antigenic peptides have been identified. These tumor-rejection antigens include tumor-specific shared antigens, differentiation antigens, or antigens specific for individual tumors. Tumor-specific CTLs have been generated from peripheral blood mononuclear cells (PBMC) of healthy donors or patients with malignant tumors by in vitro stimulation with peptide epitopes derived from tumor-rejection antigens. Furthermore, induction of peptide-specific CTL in PBMC has been observed in patients following the immunization with the antigenic peptides in vivo. Based on these findings, clinical vaccine trials using these antigenic peptides have recently begun in patients with melanoma as well as other tumors that express these antigens, and some tumor responses have been seen in a limited number of patients. Therefore, in order to evaluate the efficacy of the vaccine therapy against various malignant tumors, further clinical studies are now under way.

摘要

最近已从人黑色素瘤细胞系中分离出许多编码肿瘤抗原的基因。这些基因编码的抗原在HLA I类分子的背景下被自体细胞毒性T淋巴细胞(CTL)识别,并且已经鉴定出抗原肽。这些肿瘤排斥抗原包括肿瘤特异性共享抗原、分化抗原或个别肿瘤特有的抗原。通过用源自肿瘤排斥抗原的肽表位进行体外刺激,已从健康供体或患有恶性肿瘤的患者的外周血单核细胞(PBMC)中产生肿瘤特异性CTL。此外,在患者体内用抗原肽免疫后,在PBMC中观察到了肽特异性CTL的诱导。基于这些发现,最近已开始在黑色素瘤患者以及表达这些抗原的其他肿瘤患者中使用这些抗原肽进行临床疫苗试验,并且在少数患者中观察到了一些肿瘤反应。因此,为了评估疫苗疗法对各种恶性肿瘤的疗效,目前正在进行进一步的临床研究。

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