{"title":"A Real-Time Cytotoxicity Assay as an Alternative to the Standard Chromium-51 Release Assay for Measurement of Human NK and T Cell Cytotoxic Activity","authors":"Julien Fassy, Kyriaki Tsalkitzi, Maria Goncalves-Maia, Véronique M. Braud","doi":"10.1002/cpim.28","DOIUrl":null,"url":null,"abstract":"<p>This unit describes the monitoring and quantification of cellular cytotoxicity using a non-radioactive and real-time cytotoxic assay. The extent of target-cell lysis is monitored over time by imaging and quantifying live fluorescent target cells using a cell-imaging multimode reader. This assay is performed in a 96 well plate in optimized culture conditions at 37°C in the presence of 5% CO<sub>2</sub>. The basic protocol describes natural killer cell-mediated cytotoxic assay that can be adapted to include antibodies blocking inhibitory NK receptors or triggering antibody-dependent cell-mediated cytotoxicity (ADCC). The assay is also suitable for antigen specific T-cell cytotoxic assays. Until now, the standard chromium 51 (<sup>51</sup>Cr)-release assay has remained the sole sensitive assay but its major drawbacks include cost and hazard of handling radioactivity. The real-time cytotoxic assay is therefore an effective alternative providing a robust and sensitive assay that accurately monitors lysis of target cells over time. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":10733,"journal":{"name":"Current Protocols in Immunology","volume":"118 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpim.28","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Immunology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpim.28","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 11
Abstract
This unit describes the monitoring and quantification of cellular cytotoxicity using a non-radioactive and real-time cytotoxic assay. The extent of target-cell lysis is monitored over time by imaging and quantifying live fluorescent target cells using a cell-imaging multimode reader. This assay is performed in a 96 well plate in optimized culture conditions at 37°C in the presence of 5% CO2. The basic protocol describes natural killer cell-mediated cytotoxic assay that can be adapted to include antibodies blocking inhibitory NK receptors or triggering antibody-dependent cell-mediated cytotoxicity (ADCC). The assay is also suitable for antigen specific T-cell cytotoxic assays. Until now, the standard chromium 51 (51Cr)-release assay has remained the sole sensitive assay but its major drawbacks include cost and hazard of handling radioactivity. The real-time cytotoxic assay is therefore an effective alternative providing a robust and sensitive assay that accurately monitors lysis of target cells over time. © 2017 by John Wiley & Sons, Inc.
实时细胞毒性试验替代标准铬-51释放法测定人NK细胞和T细胞的细胞毒性活性
本单元描述了使用非放射性和实时细胞毒性测定法监测和定量细胞毒性。靶细胞裂解的程度是监测随着时间的推移成像和定量荧光靶细胞使用细胞成像多模式阅读器。本实验在96孔板中进行,最佳培养条件为37°C, 5% CO2存在。基本方案描述了自然杀伤细胞介导的细胞毒性测定,可以适应包括抗体阻断抑制性NK受体或触发抗体依赖性细胞介导的细胞毒性(ADCC)。该试验也适用于抗原特异性t细胞毒性试验。到目前为止,标准的51Cr释放法仍然是唯一灵敏的测定方法,但其主要缺点是成本高和处理放射性危险。因此,实时细胞毒性测定是一种有效的替代方法,提供了一种可靠而敏感的测定方法,可以随着时间的推移准确地监测靶细胞的裂解。©2017 by John Wiley &儿子,Inc。
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