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在大鼠结肠癌模型中使用双特异性单克隆抗体进行T细胞重定向:IV. 温氏试验中的肿瘤中和作用

T-cell retargeting using bispecific monoclonal antibodies in a rat colon carcinoma model: IV. Tumor neutralization in Winn type assays.

作者信息

Beun G D, van de Velde C J, Fleuren G J, Eggermont A M

机构信息

Department of Surgery, University of Leiden, The Netherlands.

出版信息

J Immunother Emphasis Tumor Immunol. 1993 Jul;14(1):11-5. doi: 10.1097/00002371-199307000-00002.

Abstract

We investigated the ability of bispecific anti-T-cell receptor x anti-tumor antibodies, destined for the study of T-cell retargeting in a rat colon carcinoma model, to enhance tumor neutralization by polyclonally activated CD8+ T lymphocytes in hepatic subcapsular Winn type assays against syngeneic CC531 colon carcinoma cells. Attempts to improve on initially unsatisfactory results were guided by a 3-day in vitro cocultivation assay, demonstrating that recombinant IL-2 (rIL-2) at concentrations as low as 1 U/ml would promote tumor neutralization by retargeted effector cells. Accordingly, we found that a nontoxic regimen of rIL-2 administration, 200,000 U subcutaneously every 8 h for 3 days, strongly enhanced natural killer-like as well as retargeted anti-tumor activity in Winn assays and enabled retargeted effector cells to prevent tumor growth in the majority of animals. These results back up and direct future attempts to treat established tumor lesions.

摘要

我们研究了双特异性抗T细胞受体x抗肿瘤抗体在大鼠结肠癌模型中重定向T细胞的能力,该抗体旨在通过肝包膜下Winn型试验中多克隆激活的CD8 + T淋巴细胞增强对同基因CC531结肠癌细胞的肿瘤中和作用。最初结果不尽人意,于是我们通过一项为期3天的体外共培养试验来指导改进工作,该试验表明浓度低至1 U/ml的重组白细胞介素-2(rIL-2)可促进重定向效应细胞的肿瘤中和作用。因此,我们发现一种无毒的rIL-2给药方案,即每8小时皮下注射200,000 U,持续3天,在Winn试验中可显著增强自然杀伤样以及重定向的抗肿瘤活性,并使重定向效应细胞在大多数动物中阻止肿瘤生长。这些结果为未来治疗已形成肿瘤病变的尝试提供了支持和指导。

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