Ex vivo culture of malignant primary B cells

Morgane Canonne, Fabienne George, C. Graux
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Abstract

Mature B cell malignancies constitute a wide range of biologically and clinically heterogeneous hematological diseases. Despite an increasingly thorough understanding of the pathophysiology of these pathologies and significant improvements in therapies, a dismal outcome still affects a large number of patients. Therefore, further investigations into new treatment perspectives are highly needed and they depend entirely on the ex vivo culture of patient cells. Primary cells usually demand superior culture models, as they are notoriously difficult to cultivate. The literature is not devoid of approaches ranging from two- to three-dimensional systems for culturing mature malignant primary B cells. However, they display substantial protocol inter-variation. This imposes a high risk of failures, repeats, and inconsistent results, which are neither compatible with the rare value of primary cells nor the efficiency of the drug discovery process. In this review, we provide a thorough overview of the different approaches that have been implemented in the literature for the culture of mature malignant primary B cells, and we discuss associated considerations and limitations to assist researchers in determining a fit-for-purpose culture system, thereby attempting to reduce the number of trials and errors as well as associated biomaterial expenditure.
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恶性原代B细胞的体外培养
成熟B细胞恶性肿瘤构成了广泛的生物学和临床异质性血液病。尽管对这些病理的病理生理学的理解越来越透彻,治疗方法也有了显著的改进,但令人沮丧的结果仍然影响着大量患者。因此,迫切需要进一步研究新的治疗方法,而这些方法完全依赖于患者细胞的体外培养。原代细胞通常需要更好的培养模型,因为它们是出了名的难以培养。文献并非缺乏从二维到三维系统培养成熟恶性原代B细胞的方法。然而,它们表现出实质性的协议互变。这带来了失败、重复和结果不一致的高风险,既不符合原代细胞的罕见价值,也不符合药物发现过程的效率。在这篇综述中,我们全面概述了文献中用于培养成熟恶性原代B细胞的不同方法,并讨论了相关的注意事项和局限性,以帮助研究人员确定适合目的的培养系统,从而试图减少试验和错误的数量以及相关的生物材料消耗。
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