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基于阻抗的细胞毒性检测法,用于实时、无标记评估 T 细胞介导的贴壁细胞杀伤作用。

An impedance-based cytotoxicity assay for real-time and label-free assessment of T-cell-mediated killing of adherent cells.

机构信息

Department of Immunology, Institute of Cell Biology, University of Tübingen, and German Cancer Consortium, DKFZ Partner site Tübingen, Tübingen, Germany.

Department of Immunology, Institute of Cell Biology, University of Tübingen, and German Cancer Consortium, DKFZ Partner site Tübingen, Tübingen, Germany; Department of General, Visceral and Transplant Surgery, University Hospital of Tübingen, Tübingen, Germany.

出版信息

J Immunol Methods. 2014 Mar;405:192-8. doi: 10.1016/j.jim.2014.01.012. Epub 2014 Jan 29.

Abstract

The in vitro assessment of T-cell-mediated cytotoxicity plays an important and increasingly relevant role both in preclinical target evaluation and during immunomonitoring to accompany clinical trials employing targeted immunotherapies. For a long time, the gold standard for this purpose has been the chromium release assay (CRA). This end point assay, however, shows several disadvantages including the inevitable use of radioactivity. Based on electrical impedance measurements (using the xCELLigence system), we have established a label-free assay, facilitating the real-time monitoring of T-cell-mediated cytotoxicity. The coculture of peptide-specific T-cell lines with peptide-loaded target cells reproducibly led to a decrease in impedance due to induced apoptosis and detachment of target cells. Comparing our results to the standard CRA assay, we could demonstrate that impedance-based measurements show comparable results after short incubation periods (6h) but outperform the CRA both in reproducibility and sensitivity after prolonged incubation (24h), enabling the detection of target cell lysis with an effector to target ratio as low as 0.05:1. The impedance-based assay represents a valuable and highly sensitive tool for label-free real-time high throughput analysis of T-cell-mediated cytotoxicity.

摘要

体外 T 细胞介导的细胞毒性评估在临床前靶标评估和免疫监测中都起着重要作用,以伴随使用靶向免疫疗法的临床试验。长期以来,该目的的金标准一直是铬释放测定(CRA)。然而,这种终点测定显示出几个缺点,包括不可避免地使用放射性。基于电阻抗测量(使用 xCELLigence 系统),我们建立了一种无标记测定法,方便实时监测 T 细胞介导的细胞毒性。肽特异性 T 细胞系与负载肽的靶细胞共培养可重现地导致阻抗降低,这是由于诱导的细胞凋亡和靶细胞的脱落所致。将我们的结果与标准 CRA 测定进行比较,我们可以证明,在短孵育期(6 小时)后,基于阻抗的测量显示出可比的结果,但在延长孵育期(24 小时)后,其重复性和灵敏度均优于 CRA,能够以效靶比低至 0.05:1 的方式检测到靶细胞裂解。基于阻抗的测定是一种有价值的、高度敏感的工具,用于无标记实时高通量分析 T 细胞介导的细胞毒性。

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