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肿瘤学中的细胞因子基因治疗。

Cytokine gene therapy in oncology.

作者信息

Foa R, Cignetti A, Riera L, Gillio Tos A, Guarini A

机构信息

Dipartimento di Scienze Biomediche ed Oncologia Umana, Sezione Clinica, University of Torino.

出版信息

Folia Biol (Praha). 1994;40(1-2):37-48.

PMID:7958063
Abstract

Over the last few years the possibility of introducing foreign material into the genome of host cells has become technically feasible. This has opened a new era in the treatment of congenital disorders, but has also offered potential innovative avenues in the management of cancer patients. Here, we shall discuss how cytokine genes may be successfully transduced into the DNA of different experimental tumours and how through this approach the tumorigenicity of the neoplastic cells may be abrogated. Emphasis will be given on the demonstration that following cytokine gene transfer, namely with the interleukin 2 (IL-2) gene, two of the primary goals of an optimal immunotherapeutic approach, i.e. anti-tumour specificity and memory, may be achieved. Attention will be focused, in particular, on the results so far obtained, as well as on ongoing studies, with human tumour cells engineered to release different cytokine genes. The design and activation of the first clinical protocols aimed at treating advanced cancer patients with cytokine gene-transduced neoplastic cells will also be discussed, together with other strategies of genetic engineering currently under investigation.

摘要

在过去几年里,将外源物质导入宿主细胞基因组在技术上已变得可行。这开启了先天性疾病治疗的新纪元,同时也为癌症患者的管理提供了潜在的创新途径。在此,我们将讨论细胞因子基因如何能够成功转导至不同实验性肿瘤的DNA中,以及通过这种方法如何消除肿瘤细胞的致瘤性。重点将放在以下论证上:在细胞因子基因转移后,即通过白细胞介素2(IL-2)基因转移后,可实现最佳免疫治疗方法的两个主要目标,即抗肿瘤特异性和记忆性。尤其会关注到目前为止所取得的结果,以及针对经过基因工程改造以释放不同细胞因子基因的人类肿瘤细胞所开展的正在进行的研究。还将讨论旨在用细胞因子基因转导的肿瘤细胞治疗晚期癌症患者的首个临床方案的设计与启动,以及目前正在研究的其他基因工程策略。

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