Inherited Deficiency of the Seventh Component of Complement Associated with Nephritis: <i>PROPENSITY TO FORMATION OF C5̄6̄ AND RELATED C7-CONSUMING ACTIVITY</i>

G. R. Nemerow; H. Gewurz; S. G. Osofsky; T. F. Lint

doi:10.1172/JCI109080

Inherited Deficiency of the Seventh Component of Complement Associated with Nephritis: PROPENSITY TO FORMATION OF C5̄6̄ AND RELATED C7-CONSUMING ACTIVITY

G. R. Nemerow, H. Gewurz, S. G. Osofsky, and T. F. Lint

Published June 1, 1978 - More info

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Abstract

A 46-yr-old female with chronic pyelonephritis was found to lack complement (C) activity by the use of hemolytic screen assays in agarose gels. These assays also revealed a propensity of patient serum to form an activated complex of the fifth and sixth components of C, C5̄6̄. Each of the C component hemolytic activities was present in normal or elevated amounts with the exception of C7, which was undetectable; addition of purified C7 led to the restoration of hemolytic activity. C-dependent phagocytosis, immune adherence, and neutrophil chemotaxis were normal. Family studies demonstrated that the defect was transmitted as an autosomal codominant apparently not linked with alleles at the HLA-A or HLA-B loci. Persisting C5̄6̄ was readily formed in this as compared to normal serum upon incubation with multiple C activators including zymosan, inulin, immune complexes, heat-aggregated human gamma globulin, endotoxin, and agarose. A heat-stable (56°C, 30 min) activity which consumed C7 with time-and temperature-dependent kinetics was detected in plasma and serum, and seemed to be similar to a “C7 inactivator” previously described in another C7-deficient individual. However, this activity was found to have properties identical to those of C5̄6̄ during low ionic strength precipitation and chromatography on Sephadex G-200, to be specifically removed upon passage through an anti-C5 immunoadsorbent column, and to be associated with a small amount of C5̄6̄, suggesting that it represents an expression of small amounts of C5̄6̄ rather than a new C-inhibitory activity. Thus, an individual with chronic nephritis lacking C7 is reported; the utility of a hemolytic screen assay in agarose plates for the detection of such patients is emphasized; persisting C5̄6̄ is shown readily to be formed in this serum; and the presence of C7-consuming activity which is associated with and in all likelihood attributable to C5̄6̄ is shown.

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