van Rossum Mara, Veuskens Bert R J, Brouwer Mieke C, van Mierlo Gerard, Lucientes-Continente Laura, Goicoechea de Jorge Elena, Uzonyi Barbara, Matola Alexandra T, Józsi Mihály, Müller Günter, Meter-Arkema Anita M, Poppelaars Felix, Pauly Diana, Pouw Richard B, Toonen Erik J M
R&D Department, Hycult Biotech, Uden, The Netherlands.
Sanquin Research and Landsteiner Laboratory of the Amsterdam University Medical Centers, Amsterdam, The Netherlands,
J Innate Immun. 2025;17(1):226-243. doi: 10.1159/000545139. Epub 2025 Mar 26.
The complement system's alternative pathway relies on factor H (FH) for immune homeostasis. Next to FH, a group of highly similar proteins was described known as the FH-related (FHR) proteins. The FH protein family includes FH, factor H-like protein 1, and five FHR proteins (FHR-1 to -5). The exact function of the FHRs is still unknown, necessitating further research. However, the lack of highly specific assays has hindered studying their role in health and disease. This study aimed to develop novel ELISAs for reliably and specifically quantifying levels of the FHRs in human blood.
Novel FHR-specific antibodies were generated. Positive hybridoma clones were taken to monoclonality, verified for target specificity via ELISA and Western blot, and antibody pairs were selected for further ELISA development. During development, ELISAs were characterized and validated for specificity, stability, accuracy, and reproducibility, among others.
Monoclonal antibodies specific for FHR-2, -3, -4, or -5 were generated. Using these antibodies, four ELISAs were developed capable of quantifying FHR levels in an accurate and robust manner. Each assay showed high target specificity, good analyte recovery and strong reproducibility between replicates, test runs, and test laboratories.
These assays enable specific and accurate quantification of FHR-2, -3, -4, and -5 in human blood. They facilitate large-scale screening of patient cohorts in a standardized manner and contribute to understanding the role of the FHRs in health and disease.
补体系统的替代途径依赖于因子H(FH)来维持免疫稳态。除FH外,还描述了一组高度相似的蛋白质,称为FH相关(FHR)蛋白。FH蛋白家族包括FH、类FH蛋白1和五种FHR蛋白(FHR-1至-5)。FHR的确切功能仍不清楚,需要进一步研究。然而,缺乏高度特异性的检测方法阻碍了对其在健康和疾病中作用的研究。本研究旨在开发新型酶联免疫吸附测定(ELISA)方法,以可靠且特异性地定量人血液中FHR的水平。
制备了新型FHR特异性抗体。将阳性杂交瘤克隆进行单克隆化,通过ELISA和蛋白质免疫印迹法验证其靶标特异性,并选择抗体对进一步开发ELISA。在开发过程中,对ELISA的特异性、稳定性、准确性和可重复性等进行了表征和验证。
产生了针对FHR-2、-3、-4或-5的单克隆抗体。使用这些抗体,开发了四种能够准确、可靠地定量FHR水平的ELISA。每种检测方法都显示出高靶标特异性、良好的分析物回收率以及在重复实验、不同批次实验和不同检测实验室之间的强可重复性。
这些检测方法能够特异性、准确地定量人血液中的FHR-2、-3、-4和-5。它们有助于以标准化方式对患者队列进行大规模筛查,并有助于了解FHR在健康和疾病中的作用。