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使用异源免疫测定法对血清蛋白进行定量:以犬C反应蛋白为例。

Use of heterologous immunoassays for quantification of serum proteins: The case of canine C-reactive protein.

作者信息

Muñoz-Prieto Alberto, Tvarijonaviciute Asta, Escribano Damián, Martínez-Subiela Silvia, Cerón José J

机构信息

Interdisciplinary Laboratory of Clinical Analysis, Interlab-UMU, Regional Campus of International Excellence "Campus Mare Nostrum", University of Murcia, Espinardo, Murcia, Spain.

出版信息

PLoS One. 2017 Feb 21;12(2):e0172188. doi: 10.1371/journal.pone.0172188. eCollection 2017.

Abstract

The use of heterologous immunoassays containing antibodies raised against a different biological species for quantification of serum proteins is studied and discussed, taking as example the case of the use of a commercially available heterologous assay containing antibodies against human C-reactive protein (hCRP) for quantification of CRP in serum of dogs. This assay was adapted and validated for measurements of canine CRP (cCRP) and compared with three different homologous assays containing species-specific canine antibodies, which are currently commercially available for cCRP determination. Serum samples from healthy and diseased dogs (n = 44) were used. Analytical evaluation included precision, accuracy, limit of detection and lower limit of quantification for all assays. In the case of the heterologous assay also cross-reactivity of the antibody of the heterologous assay with cCRP was evaluated by a Western-Blot analysis giving a positive result. The heterologous assay showed similar results than the homologous assays in all the tests of the analytical evaluation that indicated that the assay was precise and accurate. Method comparison showed a high correlation between all assays (r≥0.9). The Bland-Altman test revealed that the heterologous assay showed a proportional error when compared with the homologous automated assays and a random error when compared with the point-of-care assay. All four CRP assays were able to detect higher CRP values in dogs with inflammatory conditions compared with healthy dogs. It is concluded that heterologous immunoassays could be used for quantification of serum proteins in different species, provided that the antibody has cross-reactivity with the protein to be measured and the assay give satisfactory results in the analytical validation tests. In addition, use of species-specific calibrators and an appropriate batch validation are recommended in these cases.

摘要

本文以一种市售的含抗人C反应蛋白(hCRP)抗体的异源检测法用于定量犬血清中C反应蛋白(cCRP)为例,研究并讨论了使用含有针对不同生物物种产生的抗体的异源免疫检测法定量血清蛋白的情况。该检测法经调整和验证后用于测量犬C反应蛋白(cCRP),并与三种目前市售的含物种特异性犬抗体的不同同源检测法进行比较,这些同源检测法用于cCRP测定。使用了来自健康和患病犬(n = 44)的血清样本。分析评估包括所有检测法的精密度、准确度、检测限和定量下限。对于异源检测法,还通过蛋白质印迹分析评估了异源检测法抗体与cCRP的交叉反应性,结果呈阳性。在分析评估的所有测试中,异源检测法显示出与同源检测法相似的结果,表明该检测法准确且精密。方法比较显示所有检测法之间具有高度相关性(r≥0.9)。布兰德-奥特曼检验显示,与同源自动化检测法相比,异源检测法显示出比例误差,与即时检测法相比则显示出随机误差。与健康犬相比,所有四种CRP检测法都能够检测出患有炎症的犬的更高CRP值。得出的结论是,只要抗体与待测蛋白具有交叉反应性且检测法在分析验证测试中给出满意结果,异源免疫检测法可用于定量不同物种的血清蛋白。此外,在这些情况下建议使用物种特异性校准品并进行适当的批次验证。

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