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用粒细胞巨噬细胞集落刺激因子配制的半同种异体癌症疫苗用于转移性胃肠道腺癌患者:一项I期试点研究。

Semiallogeneic cancer vaccines formulated with granulocyte-macrophage colony-stimulating factor for patients with metastatic gastrointestinal adenocarcinomas: a pilot phase I study.

作者信息

Newton D A, Acierno P M, Metts M C, Baron P L, Brescia F J, Gattoni-Celli S

机构信息

Department of Radiation Oncology, Hollings Cancer Center, Medical University of South Carolina, Charleston, USA.

出版信息

J Immunother. 2001 Jan-Feb;24(1):19-26. doi: 10.1097/00002371-200101000-00003.

Abstract

The authors report the results of a phase I clinical study using semiallogeneic cancer vaccines formulated with granulocyte-macrophage colony-stimulating factor (GM-CSF) to treat patients with metastatic adenocarcinomas of the gastrointestinal tract. A specially engineered cell line, FO1-12, was used to generate semiallogeneic hybrids by fusion with patient-derived tumor cells; the hybrids express HLA class I and II haplotypes derived from both parental cells. For treatment, the vaccine was mixed with GM-CSF, irradiated, and injected intradermally into patients at weekly or biweekly intervals. Vaccinations were associated with minimal or no toxicity and showed that semiallogeneic hybrids formulated with GM-CSF can induce a specific antitumor immune response in some patients, as measured by a delayed-type hypersensitivity response to autologous tumor cells. Because of the simplicity, feasibility, and flexibility of this immunotherapeutic approach, semiallogeneic hybrid vaccines have the potential to be used in the treatment of virtually any type of cancer.

摘要

作者报告了一项I期临床研究的结果,该研究使用与粒细胞巨噬细胞集落刺激因子(GM-CSF)配制的半同种异体癌症疫苗来治疗胃肠道转移性腺癌患者。一种经过特殊工程改造的细胞系FO1-12被用于通过与患者来源的肿瘤细胞融合来产生半同种异体杂种;这些杂种表达源自两个亲代细胞的HLA I类和II类单倍型。用于治疗时,将疫苗与GM-CSF混合、照射,然后以每周或每两周一次的间隔皮内注射到患者体内。疫苗接种的毒性极小或没有毒性,并且表明与GM-CSF配制的半同种异体杂种可以在一些患者中诱导特异性抗肿瘤免疫反应,这通过对自体肿瘤细胞的迟发型超敏反应来衡量。由于这种免疫治疗方法的简单性、可行性和灵活性,半同种异体杂种疫苗有可能用于治疗几乎任何类型的癌症。

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