Functionally active complement proteins C6 and C7 detected in C6- and C7-deficient individuals

Author:

WÜRZNER R1,ORREN A2,POTTER P3,MORGAN B P4,PONARD D5,SPÄTH P6,BRAI M7,SCHULZE M1,HAPPE L1,GÖTZE O1

Affiliation:

1. Departments of Immunology, University of Göttingen, Germany

2. Molecular Immunopathology, MRC Centre, Cambridge, UK

3. Clinical Science and Immunology, University of Cape Town, South Africa

4. Medical Biochemistry, University of Wales, Cardiff, UK

5. Centre Hospitalier Regional, University of Grenoble, France

6. Blood Transfusion Service, Swiss Red Cross, Berne, Switzerland

7. Immunology, University of Palermo, Italy

Abstract

SUMMARY Two sensitive sandwich ELISAs based on monoclonal antibodies directed to native C6 and C7 allowed the detection and quantitation of these complement proteins in 20 out of 37 serum samples from individuals who had previously been classified as deficient in these proteins as assessed by immunochemical and/or functional assays. Furthermore, serum from four C6-deficient and one combined C6-/C7-deficient individual showed an increase in the terminal complement complex (TCC) and a decrease in native C6 and C7 after complement activation as assayed by specific ELISAs. Despite their (incomplete) deficiencies, these individuals therefore possess functionally active terminal complement proteins with respect to their ability to generate the TCC. As these individuals have no history of a susceptibility to neisserial infections, even low concentrations of functionally active C6 and C7 may provide sufficient protection against those micro-organisms whose destruction requires TCC formation.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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