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Performance of the QuantiFERON-Cytomegalovirus (CMV) Assay for Detection and Estimation of the Magnitude and Functionality of the CMV-Specific Gamma Interferon-Producing CD8+ T-Cell Response in Allogeneic Stem Cell Transplant Recipients

机译:QuantiFERON巨细胞病毒(CMV)检测的性能和同种异体干细胞移植受者中CMV特异性γ干扰素产生CD8 + T细胞反应的幅度和功能的估计

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摘要

The performance of the QuantiFERON-cytomegalovirus (CMV) assay was compared to that of a flow cytometry intracellular cytokine staining (ICS) method for the detection of CMV-specific gamma interferon (IFN-γ)-producing CD8+ T-cell responses in allogeneic stem cell transplant (allo-SCT) recipients and for estimations of their magnitude and functionality. A total of 90 whole-blood specimens from 23 allo-SCT recipients was analyzed by both methods. Overall, the percentage of specimens that yielded concordant results by both methods was 68.8% (κ = 0.691; 95% confidence interval [CI], 0.548 to 0.835), and the sensitivity of the QuantiFERON-CMV assay for the detection of positive IFN-γ T-cell responses (>0.2 IU/ml), taking the ICS method as the reference, was 76.3%. The magnitude of IFN-γ-producing CD8+ T-cell responses to CMV-specific peptides measured with the QuantiFERON-CMV assay correlated significantly (σ = 0.695; P = <0.001) with that of the total IFN-γ-producing CD8+ T cells and dual-functional (IFN-γ/tumor necrosis factor alpha [TNF-α] [σ = 0.652; P = <0.001] and IFN-γ/CD107a [σ = 0.690; P = <0.001]) and trifunctional (IFN-γ/TNF-α/CD107a [σ = 0.679; P = >0.001]) CMV-specific CD8+ T-cell responses, as quantitated by ICS. In summary, the data indicated that the QuantiFERON-CMV assay is less sensitive than the ICS method for the detection of CMV-specific IFN-γ-producing CD8+ T-cell responses in the allo-SCT setting. Nevertheless, it allowed the estimation of the total and polyfunctional CMV-specific IFN-γ-producing CD8+ T-cell responses in specimens that tested positive by both methods.
机译:将QuantiFERON-巨细胞病毒(CMV)检测的性能与流式细胞仪细胞内细胞因子染色(ICS)方法的性能进行了比较,以检测产生CMV的γ-干扰素(IFN-γ)的CD8 + 同种异体干细胞移植(allo-SCT)受体中的T细胞反应,以及其大小和功能的估计。两种方法共分析了来自23个异源SCT受体的90个全血标本。总体而言,两种方法均能产生一致结果的标本百分比为68.8%(κ= 0.691; 95%置信区间[CI]为0.548至0.835),并且QuantiFERON-CMV检测对于检测阳性IFN-γ的敏感性以ICS方法为参考,γT细胞应答(> 0.2 IU / ml)为76.3%。用QuantiFERON-CMV分析测得的产生IFN-γ的CD8 + T细胞对CMV特异性肽的反应幅度与总的显着相关(σ= 0.695; P = <0.001)产生IFN-γ的CD8 + T细胞和双重功能(IFN-γ/肿瘤坏死因子α[TNF-α] [σ= 0.652; P = <0.001]和IFN-γ/ CD107a [σ= 0.690; P = <0.001])和三功能(IFN-γ/TNF-α/ CD107a [σ= 0.679; P => 0.001])CMV特异性CD8 + T细胞应答,由ICS定量。总之,数据表明,在同种SCT环境中,QuantiFERON-CMV检测方法不如ICS方法灵敏,可检测产生CMV特异性IFN-γ的CD8 + T细胞应答。尽管如此,它仍可以估算出两种方法均呈阳性的标本中总的和多官能的CMV特异性IFN-γ产生CD8 + T细胞反应。

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