Dreolini Lisa, Cullen Mark, Yung Eric, Laird Lawrence, Webb John R, Nelson Brad H, Hay Kevin A, Balasundaram Miruna, Kekre Natasha, Holt Robert A
Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, BC V5Z 1L3, Canada.
Trev and Joyce Deeley Research Centre, BC Cancer, Victoria, BC V8R 6V5, Canada.
Mol Ther Methods Clin Dev. 2020 Jan 30;17:393-399. doi: 10.1016/j.omtm.2020.01.009. eCollection 2020 Jun 12.
species (spp.) bacteria can infect cell cultures, posing a potential threat to recipients of cell therapy products. Conventional testing methods are highly sensitive but typically require a minimum of 28 days to produce results. This delay is problematic if rapid results are needed to inform treatment decisions. Nucleic acid amplification technique (NAT) methods have been gaining favor for testing due to their speed and specificity; however, they must first be qualified as meeting or exceeding the sensitivity of the compendial method. We present herein a NAT method for the detection of that circumvents the need for live spp. in the test procedure by instead being qualified using spp. genomic DNA. We have demonstrated a lower limit of detection that exceeds the regulatory requirements set by Health Canada. This assay is now being used to screen clinical cell therapy products manufactured at our center.
某些细菌物种(spp.)可感染细胞培养物,对细胞治疗产品的接受者构成潜在威胁。传统检测方法高度灵敏,但通常至少需要28天才能得出结果。如果需要快速结果来为治疗决策提供依据,这种延迟就会成为问题。核酸扩增技术(NAT)方法因其速度和特异性而在检测中越来越受青睐;然而,它们首先必须被证明符合或超过药典方法的灵敏度。我们在此介绍一种用于检测的NAT方法,该方法通过使用spp.基因组DNA进行鉴定,从而在测试过程中无需活的spp.。我们已经证明了检测下限超过了加拿大卫生部设定的监管要求。该检测方法目前正用于筛选我们中心生产的临床细胞治疗产品。