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检测英夫利昔单抗水平和抗英夫利昔单抗抗体:三种不同检测方法的比较。

Detection of infliximab levels and anti-infliximab antibodies: a comparison of three different assays.

机构信息

Laboratory for Pharmaceutical Biology, KU Leuven, Leuven, Belgium.

出版信息

Aliment Pharmacol Ther. 2012 Oct;36(8):765-71. doi: 10.1111/apt.12030. Epub 2012 Aug 28.

Abstract

BACKGROUND

Formation of antibodies to infliximab (ATI) inversely correlates with functional drug levels and clinical outcome. Comparison of drug levels and anti-drug antibody monitoring is hampered by lack of standardisation.

AIM

To determine the correlation between three different assays for measuring infliximab and ATI.

METHODS

Serum samples and spiked controls (total 62) were evaluated in a blinded way in infliximab and ATI assays developed by Sanquin Amsterdam, Netherlands (A), Laboratory for Pharmaceutical Biology, KU Leuven, Belgium (B) and a commercially available kit from Biomedical Diagnostics (BMD), Paris, France (C) performed by the University Medical Center Groningen (UMCG), Netherlands.

RESULTS

All infliximab assays showed a linear quantitative correlation (Pearson r = 0.91 for A vs. B, 0.83 for A vs. C and 0.73 for B vs. C). Assay C detected infliximab in 11 samples (18%) not detected by A and B, including samples containing only ATI. All ATI assays showed a good linear correlation (Pearson r = 0.95 for A vs. B, 0.99 for A vs. C and 0.97 for B vs. C). Assay A detected ATI in five samples with low ATI that were not detected by assays B and C. Assay B did not detect ATI in three patient samples with low ATI according to assays A and C.

CONCLUSIONS

There is a good correlation of infliximab and antibodies to infliximab measurements between these assays. Nevertheless, the Biomedical Diagnostics kit detected false positive infliximab levels in 18% of the samples.

摘要

背景

抗英夫利昔单抗(ATI)抗体的形成与药物的功能水平和临床结果呈负相关。由于缺乏标准化,药物水平和抗药物抗体监测的比较受到阻碍。

目的

确定三种不同测定英夫利昔单抗和 ATI 的方法之间的相关性。

方法

以荷兰 Sanquin 阿姆斯特丹(A)、比利时鲁汶大学药学生物学实验室(B)和法国巴黎 Biomedical Diagnostics(BMD)商业试剂盒(C)开发的英夫利昔单抗和 ATI 测定法,对 62 份血清样本和加标对照品进行盲法评估。荷兰格罗宁根大学医学中心(UMCG)进行了测定。

结果

所有英夫利昔单抗测定法均显示出线性定量相关性(A 与 B 的 Pearson r 为 0.91,A 与 C 的 Pearson r 为 0.83,B 与 C 的 Pearson r 为 0.73)。测定法 C 检测到 11 份(18%)A 和 B 未检测到的样本中的英夫利昔单抗,包括仅含 ATI 的样本。所有 ATI 测定法均显示出良好的线性相关性(A 与 B 的 Pearson r 为 0.95,A 与 C 的 Pearson r 为 0.99,B 与 C 的 Pearson r 为 0.97)。测定法 A 检测到 5 份低 ATI 样本中的 ATI,而测定法 B 和 C 未检测到。测定法 B 未检测到 3 份低 ATI 患者样本中的 ATI,而测定法 A 和 C 检测到了。

结论

这些测定法之间英夫利昔单抗和抗英夫利昔单抗的测量具有良好的相关性。然而,Biomedical Diagnostics 试剂盒在 18%的样本中检测到假阳性英夫利昔单抗水平。

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