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时间分辨荧光法(TRF)检测首段尿和血清中总 IgG 和 HPV16 特异性抗体:一项比较研究。

Time-resolved fluorescence (TRF) for total IgG and HPV16-specific antibody detection in first-void urine and serum: A comparative study.

机构信息

Center for the Evaluation of Vaccination (CEV), Vaccine & Infectious Disease Institute (VAXINFECTIO), Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, Antwerp 2610, Belgium.

Center for the Evaluation of Vaccination (CEV), Vaccine & Infectious Disease Institute (VAXINFECTIO), Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, Antwerp 2610, Belgium.

出版信息

J Virol Methods. 2024 Sep;329:115003. doi: 10.1016/j.jviromet.2024.115003. Epub 2024 Jul 26.

Abstract

Recent studies demonstrated that human papillomavirus (HPV) specific immunoglobulins (IgG) are present and detectable in non-invasively collected first-void urine (FVU) samples. As IgG levels in urine are low, we evaluated the potential of a highly sensitive HPV16-specific assay based on time-resolved fluorescence, DELFIA, and compared it with three immunoassays, GST-L1-MIA, M4ELISA, and M9ELISA. A total of 225 paired serum and FVU samples from two cohorts of healthy female volunteers were analyzed. Strong Spearman rank correlations between HPV16-specific IgG results measured with DELFIA, M4ELISA, GST-L1-MIA, and M9ELISA were found for both sample types (r > 0.80). Additionally, total human IgG results, determined in all samples using HTRF human IgG kit and BioPlex Pro™ Human Isotyping Assay, were compared. Moderate correlations between total human IgG concentrations in FVU samples were found for the two total IgG assays (r ≥ 0.42, p < 0.0001), while correlations for serum were non-significant. In conclusion, the HPV16-DELFIA assay is usable for detecting HPV16-specific antibodies in FVU and serum samples. As total human IgG remains an interesting parameter for the normalization of HPV-specific IgG in FVU, the accuracy of both assays needs to be validated further.

摘要

最近的研究表明,人乳头瘤病毒(HPV)特异性免疫球蛋白(IgG)存在于非侵入性采集的首次尿液(FVU)样本中,并可检测到。由于尿液中的 IgG 水平较低,我们评估了一种基于时间分辨荧光的高度敏感的 HPV16 特异性检测方法(DELFI A)的潜力,并将其与三种免疫分析方法(GST-L1-MIA、M4ELISA 和 M9ELISA)进行了比较。共分析了来自两个健康女性志愿者队列的 225 对血清和 FVU 样本。对于两种样本类型,DELFI A、M4ELISA、GST-L1-MIA 和 M9ELISA 测量的 HPV16 特异性 IgG 结果之间均存在很强的斯皮尔曼等级相关(r>0.80)。此外,使用 HTRF 人类 IgG 试剂盒和 BioPlex ProTM 人类分型分析试剂盒在所有样本中测定了总人 IgG 结果。在 FVU 样本中,两种总 IgG 测定方法的总人 IgG 浓度之间存在中度相关性(r≥0.42,p<0.0001),而血清的相关性不显著。总之,HPV16-DELFI A 检测法可用于检测 FVU 和血清样本中的 HPV16 特异性抗体。由于总人 IgG 仍然是 FVU 中 HPV 特异性 IgG 归一化的一个有趣参数,因此需要进一步验证这两种检测方法的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b3/11406150/7d7c1367f884/gr1.jpg

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