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通过展示单链可变片段抗体的逆转录病毒将基因递送至产生癌胚抗原的癌细胞的靶向策略。

Targeting strategy for gene delivery to carcinoembryonic antigen-producing cancer cells by retrovirus displaying a single-chain variable fragment antibody.

作者信息

Konishi H, Ochiya T, Chester K A, Begent R H, Muto T, Sugimura T, Terada M

机构信息

First Department of Surgery, National Cancer Center Research Institute, University of Tokyo, Japan.

出版信息

Hum Gene Ther. 1998 Jan 20;9(2):235-48. doi: 10.1089/hum.1998.9.2-235.

Abstract

Cancer-specific antigens are promising targets for the specific delivery of certain drugs or genes to cancer cells in cancer therapy. Carcinoembryonic antigen (CEA) is one of the cancer-associated antigens predominantly detected in the gastrointestinal cancer of the colon and stomach. Targeting strategies for CEA-producing cancer cells have been thoroughly developed mainly by the production of monoclonal antibodies to CEA and further single-chain variable fragment (scFv) antibodies. Here, we have generated Moloney murine leukemia virus-derived retroviral vectors co-displaying an anti-CEA scFv-envelope chimeric protein and an unmodified envelope protein to deliver a gene for herpes simplex virus thymidine kinase (HSV-tk) or Escherichia coli beta-galactosidase. The harvested viruses successfully incorporated the chimeric envelope protein as well as the unmodified envelope into the viral particles, and specifically bound to and infected human CEA-producing cancer cells via recognition of CEA, depending on the CEA-producing phenotype of the target cells. These results may have significant implications for the use of scFv directed against tumor-specific antigens for targeting specific antigen-producing cancer cells, a potential step toward in vivo cancer therapy.

摘要

癌症特异性抗原是癌症治疗中某些药物或基因特异性递送至癌细胞的有前景的靶点。癌胚抗原(CEA)是主要在结肠癌和胃癌等胃肠道癌症中检测到的癌症相关抗原之一。主要通过产生抗CEA单克隆抗体以及进一步的单链可变片段(scFv)抗体,已经充分开发了针对产生CEA的癌细胞的靶向策略。在此,我们构建了莫洛尼鼠白血病病毒衍生的逆转录病毒载体,其共展示抗CEA scFv-包膜嵌合蛋白和未修饰的包膜蛋白,以递送单纯疱疹病毒胸苷激酶(HSV-tk)或大肠杆菌β-半乳糖苷酶的基因。收获的病毒成功地将嵌合包膜蛋白以及未修饰的包膜整合到病毒颗粒中,并根据靶细胞产生CEA的表型,通过识别CEA特异性结合并感染产生人类CEA的癌细胞。这些结果对于使用针对肿瘤特异性抗原的scFv靶向产生特异性抗原的癌细胞可能具有重要意义,这是迈向体内癌症治疗的潜在一步。

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