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应用最近邻核方法客观分析百日咳毒素诱导的聚类。

The nearest neighbor nuclei method to objectify analysis of pertussis toxin-induced clustering.

机构信息

Institute for Translational Vaccinology (Intravacc), Bilthoven, The Netherlands.

Department of Virology, Biomedical Primate Research Centre, Rijswijk, The Netherlands.

出版信息

ALTEX. 2022;39(1):140-148. doi: 10.14573/altex.2012171. Epub 2021 Oct 15.

Abstract

The in vivo histamine sensitization test (HIST) has historically been performed to guarantee the safety of acellular per­tussis vaccine batches. Non-compliance of batches is primarily associated with the presence of low levels of pertussis toxin (PTx). Because of ethical, standardization and scientific reasons, a variety of alternative in vitro approaches have been studied to replace the lethal HIST. A broadly applied and partially accepted method is the CHO cell clustering test, which is based on the clustered growth pattern of CHO cells when exposed to minute amounts of PTx. One of the major hurdles for global application of the CHO clustering test is the manual assessment of the clusters, which is associated with suboptimal reproducibility of test outcomes and is time-consuming. Here, various parameters of CHO cell nuclei were evaluated in search for a reliable, objective read-out parameter. We demonstrate that the distance between each nucleus and its nearest neighbor (3N method) is the most suitable parameter to assess clustered cell growth. This method detects 2.8 mIU PTx/mL and thereby complies with the requirement set for the sensitivity of the CHO clustering test based on visual reading. In commercial acellular pertussis vaccines spiked with PTx, the method detects 45 mIU/mL PTx, which is substantially lower than the 181-725 mIU/mL PTx detected by visual interpretation. The 3N method thus allows objective and sensitive assessment of CHO clustering and thereby encourages broad and global implementation of the in vitro test as an alternative to the HIST.

摘要

体内组氨酸致敏试验(HIST)历来用于保证无细胞百日咳疫苗批次的安全性。不合格批次主要与百日咳毒素(PTx)水平低有关。由于伦理、标准化和科学原因,已经研究了各种替代体外方法来替代致命的 HIST。一种广泛应用且部分被接受的方法是 CHO 细胞聚集试验,该试验基于 CHO 细胞在暴露于微量 PTx 时的聚集生长模式。CHO 细胞聚集试验在全球应用的主要障碍之一是对聚集的手动评估,这与测试结果的可重复性不理想且耗时有关。在这里,评估了 CHO 细胞核的各种参数,以寻找可靠的、客观的读出参数。我们证明,每个细胞核与其最近邻居之间的距离(3N 方法)是评估聚集细胞生长的最合适参数。该方法检测到 2.8 mIU PTx/mL,从而符合基于视觉读数的 CHO 聚集试验灵敏度的要求。在添加了 PTx 的商业无细胞百日咳疫苗中,该方法检测到 45 mIU/mL 的 PTx,大大低于视觉解释检测到的 181-725 mIU/mL 的 PTx。因此,3N 方法允许客观和敏感地评估 CHO 聚集,从而鼓励广泛和全球实施体外试验作为 HIST 的替代方法。

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