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PMID: 535181 Published · ppublish English Journal Article

Metabolism of human beta 1H: studies in man and experimental animals.

Clinical and experimental immunology ·Vol. 38 ·No. 3 ·1979-12-00 ·Pages 397-404

Charlesworth JA, Scott DM, Pussell BA, Peters DK

Abstract

Metabolic studies were performed with a purified, functionally-active preparation of human beta 1H. In seven normal human subjects, the half-life ranged from 66--87 hr with fractional catabolic rates (FCR) of 1.04--1.63%/hr. Synthesis rates were 0.22--0.57 mg/kg/hr and extravascular distribution ratios were 0.34--0.67. There was evidence of extra-vascular catabolism in each subject. In sixteen patients with immunological disease four showed hypercatabolism of beta 1H. However, three patients with C3 mephritis factor (NeF) had normal beta 1H turnover despite profound reduction in C3 concentration; it is suggested that the reaction of beta 1H with the C3b. Bb convertase exposes it to a catabolic site and that in the NeF patients the NeF stabilized convertase prevents such exposure. Studies of the acute phase response were carried out in nine patients following elective surgery, with C-reactive protein (CRP) used as the control protein: six patients showed no rise in beta 1H levels and three showed a small (20%) rise whereas all exhibited a gross rise in CRP. Pre-incubation of 125I- beta 1H with NHS, with NHS in the presence of NeF and with C3b+C3b 1NA caused no change in beta 1H turnover in animals despite demonstrable total C3 conversion with the NeF.

MeSH Terms
Animals Antigen-Antibody Complex Complement C3b Inactivator Proteins/metabolism Complement System Proteins/metabolism Half-Life Humans Immune System Diseases/metabolism Rabbits
Chemicals
Antigen-Antibody Complex Complement C3b Inactivator Proteins Complement System Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Charlesworth J A
Scott D M
Pussell B A
Peters D K
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18 references, click to expand
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Article Info
Journal
Clinical and experimental immunology
Abbr.
Clin Exp Immunol
ISSN
0009-9104
Published
1979-12-00
Pages
397-404
Language
English
Region
England
NLM ID
0057202
PMCID
PMC1537924
Subset
IM
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