In vivo clearance studies of the terminal fluid-phase complement complex in rabbits.

F Hugo, C Berstecher, S Krämer… - Clinical and …, 1989 - ncbi.nlm.nih.gov
F Hugo, C Berstecher, S Krämer, W Fassbender, S Bhakdi
Clinical and experimental immunology, 1989ncbi.nlm.nih.gov
The present study was directed at obtaining information on the in vivo elimination rate of
SC5b-9, the terminal fluid-phase product of complement activation. A sandwich ELISA
based on the use of mono-and polyclonal antibodies was constructed that permitted
quantitation of rabbit SC5b-9 in plasma. Rabbit serum was activated with inulin in vitro to
generate SC5b-9, and the activated serum was applied intravenously in normal and C6-
deficient rabbits. Elimination of SC5b-9 in normal rabbits was rapid, half-life in the range of …
Abstract
The present study was directed at obtaining information on the in vivo elimination rate of SC5b-9, the terminal fluid-phase product of complement activation. A sandwich ELISA based on the use of mono-and polyclonal antibodies was constructed that permitted quantitation of rabbit SC5b-9 in plasma. Rabbit serum was activated with inulin in vitro to generate SC5b-9, and the activated serum was applied intravenously in normal and C6-deficient rabbits. Elimination of SC5b-9 in normal rabbits was rapid, half-life in the range of 30-50 min. No differences were noted between the clearance of homologous rabbit and heterologous human SC5b-9, SC5b-9 concentrations returned to basal levels 2-3 h after application. Plasma of C6-deficient rabbits contained no SC5b-9 and these animals displayed an even more effective clearance capacity for the complex. Quantitative considerations indicated that basal plasma SC5b-9 levels in healthy animals result from a spontaneous turnover rate of approximately 0.2% of C5-C9 components per h. When multiple doses of SC5b-9 were injected in sequence, the same half-life and total elimination time were found as with single-dose experiments. The results demonstrate the existence of an effective clearance mechanism for SC5b-9, consistent with recent findings that SC5b-9 plasma levels are very low not only in healthy adults, but also in the majority of patients with complement-consuming diseases.
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