Alternative pathway of complement activation in full term and premature infants

Classical and alternative pathway complement levels were measured in the cord blood sera of 60 newly born infants, with weights ranging from 1200--4165 g. The impact of maternal illness and infant illness on the complement levels was also evaluated. The mean values for CH50, C3, C4, PH50, factor B,...

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Veröffentlicht in:Pediatric research 1979-05, Vol.13 (5 Pt 1), p.641-643
Hauptverfasser: Strunk, R C, Fenton, L J, Gaines, J A
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Gaines, J A
description Classical and alternative pathway complement levels were measured in the cord blood sera of 60 newly born infants, with weights ranging from 1200--4165 g. The impact of maternal illness and infant illness on the complement levels was also evaluated. The mean values for CH50, C3, C4, PH50, factor B, and properdin were all significantly less than normal adult levels (P less than 0.0001). All of the above determinations were significantly correlated with one another except for the relationship between properdin and factor B. CH50, PH50, C4, and properdin levels were significantly correlated with birth weight although there was much residual scatter. Neither maternal illness nor mild to moderate illness in the newborn altered the birth weight-complement relationships. Severe infant illness did significantly alter the relationship between birth weight and complement. However, the impact of this variable on the birth weight-complement relationships was not consistent among the various components. These inconsistencies and the small sample size preclude drawing any strong conclusions about severe illness and complement levels.
doi_str_mv 10.1203/00006450-197905000-00013
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source MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection; SpringerLink Journals - AutoHoldings; Journals@Ovid Complete
subjects Adult
Birth Weight
Complement Activation
Complement Pathway, Alternative
Female
Humans
Infant, Newborn
Infant, Newborn, Diseases - immunology
Infant, Premature
Pregnancy
Pregnancy Complications
title Alternative pathway of complement activation in full term and premature infants
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