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Published on: June 15, 2019
Evaluation of a Novel Immunoassay for Quantification of C1q for Clinical Diagnostic Use
Kerstin Sandholm1, Barbro Persson2, Lillemor Skattum3
1Linnaeus Center of Biomaterials Chemistry, Linnaeus University, Kalmar, Sweden.
Insights
A new magnetic bead-based sandwich immunoassay (MBSI) accurately quantifies C1q, a biomarker for systemic lupus erythematosus (SLE) disease activity. This assay is a suitable replacement for older methods, offering improved reliability in monitoring SLE patients.
Area of Science:
- Immunology
- Biochemistry
- Clinical Chemistry
Background:
- Complement component 1q (C1q) is a critical biomarker for assessing disease activity in systemic lupus erythematosus (SLE).
- Traditional C1q quantification methods like rocket immunoelectrophoresis (RIE) are time-consuming.
- Soluble immune precipitation techniques, such as nephelometry, have been adopted but face challenges due to C1q's antibody-binding properties.
Purpose of the Study:
- To compare the performance of various C1q quantification techniques, including RIE, nephelometry, and ELISA.
- To develop and validate a novel magnetic bead-based sandwich immunoassay (MBSI) for C1q measurement.
- To assess the suitability of MBSI for monitoring SLE disease activity and compare it with established methods.
Main Methods:
- Quantified C1q in serum and plasma samples from SLE patients and controls using RIE, nephelometry, and the new MBSI.
- Analyzed cerebrospinal fluid (CSF) samples using MBSI to evaluate its performance in low-detection ranges.
- Correlated MBSI results with RIE, ELISA, and clinical disease activity scores (SLEDAI and BILAG).
Main Results:
- The MBSI showed strong correlations with RIE and ELISA, but not with nephelometry.
- MBSI detected significantly lower C1q levels in SLE patients compared to controls, and lower levels in nephritis patients versus non-nephritis patients.
- Nephelometry results were unreliable, likely due to interference from C1q and anti-C1q antibodies, while MBSI accurately measured low C1q concentrations in both serum and CSF.
Conclusions:
- The developed MBSI is a reliable and accurate method for quantifying C1q, correlating well with the gold standard RIE.
- Soluble immune precipitation techniques like nephelometry are not suitable for C1q quantification due to measurement interferences.
- The MBSI offers a viable and improved alternative for monitoring C1q levels and SLE disease activity.
Abstract:
Objectives: C1q is a valuable biomarker of disease activity in systemic lupus erythematosus (SLE). The "gold standard" assay, rocket immunoelectrophoresis (RIE), is time-consuming, and thus a shift to soluble immune precipitation techniques such as nephelometry has occurred. However, quantification of C1q with these techniques has been questioned as a result of the antibody binding properties of C1q. In the present work, we have compared results using various techniques (RIE, nephelometry, and ELISA) and have developed and validated a new magnetic bead-based sandwich immunoassay (MBSI). Methods: C1q was quantified by nephelometry and the new sandwich immunoassay in 45 serum samples analyzed using RIE. C1q was also assessed in plasma using RIE and sandwich immunoassay in samples from SLE patients with nephritis (n = 69), SLE patients without nephritis (n = 310) as classified by BILAG score, and matched controls (n = 322). In addition, cerebrospinal fluid (CSF) samples from 31 patients, previously analyzed with ELISA, were also analyzed with the MBSI to test the behavior of this new assay in the lower detection range. Results: We found a strong correlation between the new MBSI, RIE, and ELISA, but not with nephelometry. The MBSI demonstrated lower levels of C1q in SLE patients than in matched controls (p < 0.0001), and patients with nephritis had lower levels than patients without nephritis (p < 0.01). Similarily, RIE showed significant differences between the patient groups (p < 0.0001). An association was also found between the levels of C1q and the SLE disease activity index (SLEDAI). Furthermore, there was good correlation between the values obtained by MBSI and ELISA, in both serum (r = 0.960) and CSF (r = 0.786), underscoring the ability of both techniques to measure low concentrations of C1q with high accuracy. Conclusion: The sandwich immunoassay correlated well with RIE, but soluble immune precipitation techniques, such as nephelometry, did not appear suitable alternatives, since C1q itself, and possibly anti-C1q antibodies, interfered with the measurements. The new sandwich immunoassay is therefore a good replacement for RIE in monitoring SLE disease activity.
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