{"title":"Antibody-Based CAR T Cells Produced by Lentiviral Transduction.","authors":"Sabrina Prommersberger, Michael Hudecek, Thomas Nerreter","doi":"10.1002/cpim.93","DOIUrl":null,"url":null,"abstract":"<p><p>One promising approach to treat hematologic malignancies is the usage of patient-derived CAR T cells. There are continuous efforts to improve the function of these cells, to optimize their receptor, and to use them for the treatment of additional types of cancer and especially solid tumors. In this protocol, an easy and reliable approach for CAR T cell generation is described. T cells are first isolated from peripheral blood (here: leukoreduction system chambers) and afterwards activated for one day with anti-CD3/CD28 Dynabeads. The gene transfer is performed by lentiviral transduction and gene transfer rate can be verified by flowcytometric analysis. Six days after transduction, the stimulatory Dynabeads are removed. T cells are cultured in interleukin-2 conditioned medium for several days for expansion. There is an option to expand CAR T cells further by co-incubation with irradiated, antigen-expressing feeder cell lines. The CAR T cells are ready to use after 10 (without feeder cell expansion) to 24 days (with feeder cell expansion). © 2020 The Authors. Basic Protocol: Generation of CAR T cells by lentiviral transduction.</p>","PeriodicalId":10733,"journal":{"name":"Current Protocols in Immunology","volume":"128 1","pages":"e93"},"PeriodicalIF":0.0000,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpim.93","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpim.93","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: 7
Abstract
One promising approach to treat hematologic malignancies is the usage of patient-derived CAR T cells. There are continuous efforts to improve the function of these cells, to optimize their receptor, and to use them for the treatment of additional types of cancer and especially solid tumors. In this protocol, an easy and reliable approach for CAR T cell generation is described. T cells are first isolated from peripheral blood (here: leukoreduction system chambers) and afterwards activated for one day with anti-CD3/CD28 Dynabeads. The gene transfer is performed by lentiviral transduction and gene transfer rate can be verified by flowcytometric analysis. Six days after transduction, the stimulatory Dynabeads are removed. T cells are cultured in interleukin-2 conditioned medium for several days for expansion. There is an option to expand CAR T cells further by co-incubation with irradiated, antigen-expressing feeder cell lines. The CAR T cells are ready to use after 10 (without feeder cell expansion) to 24 days (with feeder cell expansion). © 2020 The Authors. Basic Protocol: Generation of CAR T cells by lentiviral transduction.
慢病毒转导产生的基于抗体的CAR - T细胞
一种有希望的治疗血液恶性肿瘤的方法是使用患者来源的CAR - T细胞。人们一直在努力改善这些细胞的功能,优化它们的受体,并将它们用于治疗其他类型的癌症,特别是实体瘤。在本协议中,描述了一种简单可靠的CAR - T细胞生成方法。首先从外周血中分离T细胞(如图:白细胞诱导系统室),然后用抗cd3 /CD28 dynabheads激活一天。基因转移是通过慢病毒转导进行的,基因转移率可以通过流式细胞术分析来验证。转导6天后,移除刺激dynabheads。T细胞在白细胞介素-2条件培养基中培养数天进行扩增。通过与辐照过的表达抗原的饲养细胞系共孵育,可以进一步扩增CAR - T细胞。CAR - T细胞在10天(未扩增饲养细胞)至24天(扩增饲养细胞)后即可使用。©2020作者。基本方案:通过慢病毒转导产生CAR - T细胞。
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