Selective C3 deficiency due to C3 nephritic factor in an apparently healthy girl
- 1 October 1985
- journal article
- research article
- Published by Springer Nature in La Ricerca in Clinica e in Laboratorio
- Vol. 15 (4) , 323-329
- https://doi.org/10.1007/bf03029146
Abstract
Summary Routine laboratory investigations performed on the serum of an 8-year-old girl examined because of a moderate degree of iron-deficiency anemia showed a markedly reduced C3 level. More detailed complement studies revealed a selective C3 deficiency, as indicated by the almost undetectable C3 concentration tested by both hemolytic and immunochemical assays and by the normal or slightly reduced levels of all the other complement components. The hemolytic activity of the serum was restored by the addition of partially purified C3 component. The isolated C3 deficiency could be attributed to the presence of a C3-cleaving activity in the serum of the propositus. This activity was identified as C3 nephritic factor (C3NeF) since it was heat-stable, was absorbed by Cowan I strain ofStaphylococcus aureus and was eluted in the IgG fraction after DEAE-chromatography of the serum. The levels of H and I factors of the alternative pathway in the serum of the propositus and of C3 in the serum samples of her parents and two siblings were found to be within the normal range. The previous clinical history of the girl and the follow-up for a period of approximately 5 years showed that she was apparently healthy and did not reveal clinical and/or laboratory evidence of glomerulonephritis, lipodystrophy or repeated bacterial infections usually associated with the presence of C3NeF in the serum.Keywords
This publication has 19 references indexed in Scilit:
- Disorders of the complement system in lipodystrophyPublished by Elsevier ,2004
- Recurrent Bacterial Infections Associated with C3 Nephritic Factor and HypocomplementemiaNew England Journal of Medicine, 1983
- Two types of dysfunctional eighth component of complement (C8) molecules in C8 deficiency in man. Reconstitution of normal C8 from the mixture of two abnormal C8 molecules.Journal of Clinical Investigation, 1983
- A familial dysfunction of the eighth component of complement (C8)Clinical Immunology and Immunopathology, 1980
- C3 activator and hypocomplementaemia in a "healthy" woman.BMJ, 1976
- The use of protein A‐containing Staphylococcus aureus as a solid phase anti‐IgG reagent in radioimmunoassays as exemplified in the quantitation of α‐fetoprotein in normal human adult serumEuropean Journal of Immunology, 1974
- MESANGIOCAPILLARY NEPHRITIS, PARTIAL LIPODYSTROPHY, AND HYPOCOMPLEMENTÆMIAThe Lancet, 1973
- PARTIAL LIPODYSTROPHY AND HYPOCOMPLEMENTÆMIC NEPHRITISThe Lancet, 1973
- CHARACTERISTICS OF A NON-COMPLEMENT-DEPENDENT C3-REACTIVE COMPLEX FORMED FROM FACTORS IN NEPHRITIC AND NORMAL SERUMThe Journal of Experimental Medicine, 1970
- Serum C′3 Lytic System in Patients with GlomerulonephritisScience, 1969