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采用多重检测法评估干血斑以检测近期HIV-1感染。

Evaluation of dried blood spots with a multiplex assay for measuring recent HIV-1 infection.

作者信息

Curtis Kelly A, Ambrose Krystin M, Kennedy M Susan, Owen S Michele

机构信息

Laboratory Branch, Division of HIV/AIDS Prevention, National Center for HIV/AIDS, Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

出版信息

PLoS One. 2014 Sep 18;9(9):e107153. doi: 10.1371/journal.pone.0107153. eCollection 2014.

Abstract

Laboratory-based HIV tests for recent infection (TRIs), which primarily measure a specific serological biomarker(s) that distinguishes recent from long-term HIV infection, have facilitated the estimation of population-based incidence. Dried blood spots (DBS) on filter paper are an attractive sample source for HIV surveillance, given the simplified and cost-effective methods of specimen collection, storage, and shipment. Here, we evaluated the use of DBS in conjunction with an in-house multiplex TRI, the HIV-1-specific Bio-Plex assay, which measures direct antibody binding and avidity to multiple HIV-1 analytes. The assay performance was comparable between matched plasma and DBS samples from HIV-1 infected individuals obtained from diverse sources. The coefficients of variation, comparing the median antibody reactivity for each analyte between plasma and DBS, ranged from 2.78% to 9.40% and the correlation coefficients between the two sample types ranged from 0.89 to 0.97, depending on the analyte. The correlation in antibody reactivity between laboratory and site-prepared DBS for each analyte ranged from 0.87 to 0.98 and from 0.90 to 0.97 between site-prepared DBS and plasma. The correlation in assay measures between plasma and DBS indicate that the sample types can be used interchangeably with the Bio-Plex format, without negatively impacting the misclassification rate of the assay.

摘要

用于近期感染检测(TRIs)的基于实验室的HIV检测主要是测量一种特定的血清生物标志物,以区分近期HIV感染和长期HIV感染,这有助于估计基于人群的发病率。鉴于滤纸干血斑(DBS)在标本采集、储存和运输方面方法简便且成本效益高,它是HIV监测中颇具吸引力的样本来源。在此,我们评估了DBS与一种内部多重TRI(即HIV-1特异性生物芯片检测法)结合使用的情况,该检测法可测量针对多种HIV-1分析物的直接抗体结合及亲和力。来自不同来源的HIV-1感染个体的匹配血浆样本和DBS样本之间的检测性能相当。血浆和DBS之间每种分析物的中位数抗体反应性比较的变异系数在2.78%至9.40%之间,两种样本类型之间的相关系数在0.89至0.97之间,具体取决于分析物。每种分析物的实验室制备DBS与现场制备DBS之间的抗体反应性相关性在0.87至0.98之间,现场制备DBS与血浆之间的相关性在0.90至0.97之间。血浆和DBS之间检测指标的相关性表明,在生物芯片检测形式中,这两种样本类型可互换使用,而不会对检测的错误分类率产生负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb59/4169399/e19b3643d8fd/pone.0107153.g001.jpg

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