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从杂交瘤到T细胞表达的嵌合抗原受体制备

Chimeric antigen receptor preparation from hybridoma to T-cell expression.

作者信息

Köksal Hakan, Baken Elizabeth, Warren David John, Løset Geir Åge, Inderberg Else Marit, Wälchli Sébastien

机构信息

Department of Cellular Therapy, Department of Oncology, Oslo University Hospital-Radiumhospitalet, Oslo 0379, Norway.

Department of Medical Biochemistry, Oslo University Hospital-Radiumhospitalet, Oslo 0379, Norway.

出版信息

Antib Ther. 2019 May 31;2(2):56-63. doi: 10.1093/abt/tbz007. eCollection 2019 Apr.

Abstract

The successful use of chimeric antigen receptor (CAR) for hematological cancer treatment has influenced the direction taken in translational research toward an increasing focus on personalized targeted immunotherapy. Thus, a growing number of labs worldwide are now interested in testing their old antibody collections in this format to broaden the spectrum of utility and improve safety and efficacy. We herein present a straightforward protocol for the identification of an antibody from a hybridoma and the design of the single chain fragment that will be placed on the extracellular part of the CAR construct. We further show how to test the expression and the activity of the construct in primary T cells. We illustrate our demonstration with two new CARs targeted against the B cell receptor, more precisely the light chains κ and λ, that represent potential alternatives to the CD19 CAR used in the treatment of B-cell malignancies.

摘要

嵌合抗原受体(CAR)在血液系统癌症治疗中的成功应用影响了转化研究的方向,使其越来越关注个性化靶向免疫疗法。因此,全球越来越多的实验室现在有兴趣以这种形式测试他们原有的抗体库,以拓宽应用范围并提高安全性和有效性。我们在此提出一种直接的方案,用于从杂交瘤中鉴定抗体并设计将置于CAR构建体细胞外部分的单链片段。我们还展示了如何在原代T细胞中测试构建体的表达和活性。我们用两种针对B细胞受体(更确切地说是κ和λ轻链)的新型CAR进行演示,它们代表了用于治疗B细胞恶性肿瘤的CD19 CAR的潜在替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a933/7990154/9c098602feef/tbz007f1.jpg

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