Connie MacKinnon , Ryan McLean , Antonia L. Pritchard
{"title":"Lymphoblastoid cell lines do not recapitulate physiological circulating B cell subtypes","authors":"Connie MacKinnon , Ryan McLean , Antonia L. Pritchard","doi":"10.1016/j.crimmu.2024.100079","DOIUrl":null,"url":null,"abstract":"<div><p>Lymphoblastoid cell lines (LCLs) are immortalised peripheral B lymphocytes, transformed via infection with Epstein Barr virus (EBV). The use of LCLs to study B cell function remains controversial and core markers to define physiological B cell populations are not consistent between studies of physiological B cells and LCLs. A consensus on the nature of these commonly used cell lines has not been reached. Recently, a core set of markers to subtype peripheral B cells was proposed, addressing the lack of agreed markers for B cell characterisation. In this present study, the consensus panel was applied to describe the B cell subtypes in LCLs. We found that LCLs were generally not physiologically representative of B cells, with most cells harbouring marker combinations absent on peripheral B cells. Some B cell subtyping markers were fundamentally altered during EBV transformation to LCLs (e.g. CD19, CD21). Notably, most LCLs secreted IgG but the associated marker combinations were predominantly only present <em>in vitro</em> following EBV transformation. This study therefore informs interpretation of past investigations, and planning of future studies using LCLs, as these cells are unlikely to behave like their pre-transformed B cell subtype.</p></div>","PeriodicalId":72750,"journal":{"name":"Current research in immunology","volume":"5 ","pages":"Article 100079"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590255524000039/pdfft?md5=3e72ca03bcf11cf8a3b7ad431366c3fc&pid=1-s2.0-S2590255524000039-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current research in immunology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590255524000039","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 0
Abstract
Lymphoblastoid cell lines (LCLs) are immortalised peripheral B lymphocytes, transformed via infection with Epstein Barr virus (EBV). The use of LCLs to study B cell function remains controversial and core markers to define physiological B cell populations are not consistent between studies of physiological B cells and LCLs. A consensus on the nature of these commonly used cell lines has not been reached. Recently, a core set of markers to subtype peripheral B cells was proposed, addressing the lack of agreed markers for B cell characterisation. In this present study, the consensus panel was applied to describe the B cell subtypes in LCLs. We found that LCLs were generally not physiologically representative of B cells, with most cells harbouring marker combinations absent on peripheral B cells. Some B cell subtyping markers were fundamentally altered during EBV transformation to LCLs (e.g. CD19, CD21). Notably, most LCLs secreted IgG but the associated marker combinations were predominantly only present in vitro following EBV transformation. This study therefore informs interpretation of past investigations, and planning of future studies using LCLs, as these cells are unlikely to behave like their pre-transformed B cell subtype.
淋巴母细胞系(LCL)是通过感染爱泼斯坦巴氏病毒(EBV)转化而来的永生外周 B 淋巴细胞。使用淋巴母细胞系研究 B 细胞功能仍存在争议,生理 B 细胞和淋巴母细胞系研究中用于定义生理 B 细胞群的核心标志物并不一致。人们尚未就这些常用细胞系的性质达成共识。最近,有人提出了一套用于外周 B 细胞亚型的核心标志物,以解决 B 细胞特征描述缺乏一致标志物的问题。在本研究中,该共识小组被用于描述 LCL 中的 B 细胞亚型。我们发现,LCL 在生理上通常并不代表 B 细胞,大多数细胞都带有外周 B 细胞所没有的标记物组合。在 EBV 向 LCLs 转化的过程中,一些 B 细胞亚型标记发生了根本性改变(如 CD19、CD21)。值得注意的是,大多数 LCLs 会分泌 IgG,但相关的标志物组合主要只存在于 EBV 转化后的体外。因此,这项研究为解释过去的研究和规划未来使用 LCLs 进行的研究提供了信息,因为这些细胞的行为不太可能像其转化前的 B 细胞亚型。