Usefulness and analytical performances of complement multiplex assay for measuring complement biomarkers in plasma

补体系统 C4A型 补语(音乐) 多路复用 替代补体途径 补体成分5 系数H 免疫学 计算生物学 化学 抗体 生物 生物化学 生物信息学 互补 基因 表型
作者
Marie-Sophie Meuleman,Anna Duval,Anne Grünenwald,Mikel Rezola Artero,Mohamed Dermani,Julie Peliconi,Margot Revel,Paula Vieira-Martins,Marie Courbebaisse,Béatrice Parfait,David Lebeaux,Gérard Friedlander,Lubka T. Roumenina,Sophie Chauvet,Véronique Frémeaux‐Bacchi,Marie‐Agnès Dragon‐Durey
出处
期刊:Clinica Chimica Acta [Elsevier]
卷期号:554: 117750-117750 被引量:13
标识
DOI:10.1016/j.cca.2023.117750
摘要

The complement system is involved in numerous diseases, through diverse mechanisms and degree of activation. With the emergence of complement targeting therapeutic, simple and accessible tools to evaluate the extent of complement activation are strongly needed. We evaluated two multiplex panels, measuring complement activation fragments (C4a, C3a, C5a, Bb, Ba, sC5b9) and intact components or regulators (C1q, C2, C3, C4, C5, FD, FP, FH, FI). The specificity of each measurement was assessed by using complement proteins depleted sera and plasma collected from patients with complement deficiencies. Normal values distribution was estimated using 124 plasma samples from healthy donors and complement activation profile was assessed in plasma collected from 31 patients with various complement-mediated disorders. We observed good inter-assay variation. All tested protein deficiencies were accurately detected. We established assay-specific reference values for each analyte. Except for C3, C4 and C4a, the majority of the measurements were in good agreement with references methods or published data. Our study substantiates the utility of the Complement Multiplex assay as a tool for measuring complement activation and deficiencies. Quantifying complement cleavage fragments in patients exhibiting classical or alternative pathway activation allowed evaluating the activation state of the whole cascade.
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