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Fit-for-purpose quantitative liquid biopsy based droplet digital PCR assay development for detection of programmed cell death ligand-1 (PD-L1) RNA expression in PAXgene blood samples

机译:基于型定量液检的液体活检基于液滴数字PCR测定的检测,用于检测Paxgene血液样品中的细胞死亡配体-1(PD-L1)RNA表达的检测

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摘要

Development of a clinically applicable liquid biopsy-based test for PD-L1 mRNA expression would be beneficial in providing complementary evidence to current immunohistochemistry assays. Hence, we report the development of a fit-for-purpose assay for detection of blood PD-L1 mRNA expression using droplet digital polymerase chain reaction (ddPCR). TaqMan® assays were selected based on coverage of the PD-L1 gene and were tested for linearity and efficiency using real-time quantitative PCR. Four reference genes were analyzed in positive control cell line (A549 treated with interferon gamma, [IFN γ]) genomic DNA. The PD-L1 primer/probe sets were also evaluated in ddPCR for limit of blank, limit of detection, and precision. Finally, thirty-five healthy volunteer samples were evaluated to establish a baseline level of PD-L1 expression. In ddPCR, the limit of blank was determined to be 0 copies and the limit of detection was determined to be less than or equal to 19 copies of PD-L1. The average intra-run coefficient of variation in the ddPCR assay was 7.44% and average inter-run CV was 7.70%. Treatment of A549 cells with IFN γ resulted in a 6.7-fold increase in PD-L1 expression (21,580 copies in untreated cDNA versus 145,000 copies in treated cDNA). Analysis of healthy human samples yielded a median value of 1659 PD-L1 copies/μL with a range of 768-7510 copies/μL. The assay was transferred to an external service provider and results from our in-house experiments and those conducted externally shows a correlation of 0.994. In conclusion, a fit-for-purpose liquid biopsy-based, purely quantitative ddPCR assay for the detection of PD-L1 mRNA expression was developed and validated using PAXgene RNA blood samples. Linearity, reproducibility, limit of blank and limit of detection were measured and deemed suitable for clinical application. This ultra-sensitive liquid biopsy ddPCR assay has promising clinical potential in screening, longitudinal monitoring and disease progression detection.
机译:开发PD-L1 mRNA表达的临床应用基于液检的试验将有利于为目前的免疫组织化学测定提供互补证据。因此,我们报告了使用液滴数字聚合酶链反应(DDPCR)检测血液PD-L1 mRNA表达的适当试验的开发。基于PD-L1基因的覆盖率选择Taqman®测定,并使用实时定量PCR测试线性度和效率。在阳性对照细胞系中分析四种参考基因(用干扰素γ,[IFNγ])基因组DNA处理A549。在DDPCR中也评估PD-L1引物/探针组,以限制空白,检测极限和精度。最后,评估了三十五个健康的志愿者样品,以建立PD-L1表达的基线水平。在DDPCR中,确定坯料的极限为0份,测定检测限为小于或等于PD-L1的19份。 DDPCR测定中的平均变异变异系数为7.44%,平均运行间Cv为7.70%。用IFNγ处理A549细胞导致PD-L1表达的增加6.7倍(未处理的cDNA中的21,580份,与治疗的cDNA中的145,000份)。健康人样品的分析产生1659pd-L1拷贝/μl的中值值,范围为768-7510拷贝/μl。该试验被转移到外部服务提供者,并由我们内部实验结果,外部进行的结果显示为0.994的相关性。总之,用于检测PD-L1 mRNA表达的适合液检,纯定量DDPCR测定并使用Paxgene RNA血液样品进行验证。测量和检测空白的线性,再现性,空白极限,适用于临床应用。这种超敏液体活检DDPCR测定具有临床潜力,筛选,纵向监测和疾病进展检测。

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