Your browser doesn't support javascript.
loading
Usefulness and analytical performances of complement multiplex assay for measuring complement biomarkers in plasma.
Meuleman, Marie-Sophie; Duval, Anna; Grunenwald, Anne; Rezola Artero, Mikel; Dermani, Mohamed; Peliconi, Julie; Revel, Margot; Vieira-Martins, Paula; Courbebaisse, Marie; Parfait, Béatrice; Lebeaux, David; Friedlander, Gérard; Roumenina, Lubka; Chauvet, Sophie; Frémeaux-Bacchi, Véronique; Dragon-Durey, Marie-Agnès.
Affiliation
  • Meuleman MS; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France; Laboratory of Immunology, Georges Pompidou European Hospital, APHP, Paris, France.
  • Duval A; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France; Department of Nephrology, Strasbourg University Hospital, Strasbourg, France.
  • Grunenwald A; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France; Department of Nephrology, Poissy Intercommunal Hospital, Poissy, France.
  • Rezola Artero M; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France.
  • Dermani M; Laboratory of Immunology, Georges Pompidou European Hospital, APHP, Paris, France.
  • Peliconi J; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France.
  • Revel M; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France.
  • Vieira-Martins P; Laboratory of Immunology, Georges Pompidou European Hospital, APHP, Paris, France.
  • Courbebaisse M; Paris Cité University, Physiology Department, European Georges-Pompidou Hospital, APHP, INSERM U1151, Paris, France.
  • Parfait B; Centre de Ressources Biologiques - site Cochin, Fédération des CRB/PRB, DMU BioPhyGen, AP-HP.Centre-Université Paris Cité, Hôpital Cochin, Paris, France.
  • Lebeaux D; Institut Pasteur, Université Paris Cité, CNRS UMR 6047, Genetics of Biofilms Laboratory, 75015 Paris, France; Service de Microbiologie, Unité Mobile d'Infectiologie, AP-HP, Hôpital Européen Georges Pompidou, 20 rue Leblanc, 75015 Paris, France.
  • Friedlander G; Fondation Université Paris Cité, Paris, France.
  • Roumenina L; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France.
  • Chauvet S; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France; Paris Cité University, Paris, France; Department of Nephrology, Georges Pompidou European Hospital, APHP, Paris, France.
  • Frémeaux-Bacchi V; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France; Laboratory of Immunology, Georges Pompidou European Hospital, APHP, Paris, France.
  • Dragon-Durey MA; Centre de Recherche des Cordeliers, Sorbonne Université, Inserm, Université Paris Cité, Inflammation, Complement and Cancer Team, Paris, France; Laboratory of Immunology, Georges Pompidou European Hospital, APHP, Paris, France; Paris Cité University, Paris, France. Electronic address: marie-agnes.du
Clin Chim Acta ; 554: 117750, 2024 Feb 01.
Article in En | MEDLINE | ID: mdl-38176523
ABSTRACT

INTRODUCTION:

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.

METHODS:

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.

RESULTS:

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.

CONCLUSION:

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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Complement System Proteins / Complement Activation Limits: Humans Language: En Journal: Clin Chim Acta Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Complement System Proteins / Complement Activation Limits: Humans Language: En Journal: Clin Chim Acta Year: 2024 Document type: Article Affiliation country:
...