Kertesz G, Bourcier B, Cailla H, Jean F
Immunotech, Marseille, France.
Clin Chem. 1998 Jan;44(1):78-85.
In this paper we describe the development and the evaluation of a new type of immunoassay for human corticotropin (ACTH). We succeeded, by using an original approach based upon immunization with ACTH derivatized with succinic anhydride, in raising monoclonal antibodies against this poorly immunogenic peptide. Three of the antibodies were selected to develop an immunoassay for ACTH. The assay requires the prior succinylation of the plasma samples for optimal sensitivity and specificity. This acylation treatment is fast, reproducible, and, in addition, improves the stability of the ACTH molecule in plasma, thus facilitating sample handling. The assay is performed in only 3 h with a detection limit of 0.7 ng/L. Analytical evaluation showed excellent specificity, reproducibility, and reliability. A comparison with two commonly used but time-consuming ACTH IRMAs was carried out by assaying several plasma samples in parallel and gave in both cases very good correlation.
在本文中,我们描述了一种新型人促肾上腺皮质激素(ACTH)免疫测定法的开发与评估。我们通过基于用琥珀酸酐衍生化的ACTH进行免疫的原始方法,成功制备了针对这种免疫原性较差的肽的单克隆抗体。选择了三种抗体来开发ACTH免疫测定法。该测定法要求血浆样本预先进行琥珀酰化以获得最佳的灵敏度和特异性。这种酰化处理快速、可重复,此外,还提高了ACTH分子在血浆中的稳定性,从而便于样本处理。该测定法仅需3小时即可完成,检测限为0.7 ng/L。分析评估显示出优异的特异性、重现性和可靠性。通过同时检测多个血浆样本,与两种常用但耗时的ACTH免疫放射测定法进行了比较,两种方法的相关性都非常好。