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Published on: September 9, 2012
Complement factor 9 deficiency in serum of human neonates
H A Lassiter1, S W Watson, M L Seifring
1Department of Pediatrics, University of Louisville School of Medicine, Kentucky.
Insights
Neonatal sera have lower concentrations of complement factor C9 (C9), leading to inefficient killing of Escherichia coli. Supplementing with C9 and IgG improved bacterial killing in neonates.
Area of Science:
- Immunology
- Neonatal Immunology
Background:
- Neonates exhibit a less developed immune system compared to adults.
- The complement system, particularly the terminal pathway involving complement factor C9 (C9), plays a crucial role in innate immunity and bacterial clearance.
Purpose of the Study:
- To investigate the concentration and functional activity of C9 in neonatal sera.
- To assess the bactericidal capacity of neonatal sera against Escherichia coli.
- To determine the effect of supplemental C9 and IgG on neonatal serum bactericidal activity.
Main Methods:
- Quantification of C9 serum concentrations in mothers and neonates.
- Assessment of serum bactericidal activity against Escherichia coli O7w:K1:NM.
- Evaluation of the impact of exogenous C9 and IgG supplementation on bacterial killing and C9 deposition.
Main Results:
- Neonatal sera showed significantly lower C9 concentrations (less than 42 µg/ml) compared to maternal sera (260 ± 47 µg/ml).
- Neonatal sera demonstrated reduced bactericidal activity against E. coli, with only 3 of 14 samples significantly reducing bacterial survival.
- Supplementation with C9 enhanced the bactericidal capacity of neonatal sera, and supplemental IgG further potentiated C9 deposition and bacterial killing.
Conclusions:
- Neonatal sera possess diminished concentrations of C9, contributing to impaired bactericidal function against E. coli.
- Exogenous C9 can restore and enhance the bactericidal activity of neonatal sera.
- The combined presence of C9 and IgG is crucial for effective bacterial clearance in neonates, highlighting potential therapeutic targets.
Abstract:
The serum concentration of complement factor C9 (C9) was 260 +/- 47 micrograms/ml (+/- SE) in 14 mothers and less than 42 micrograms/ml in each of their 14 neonates. During incubation for 60 min, 11 of 14 maternal sera and 3 of 14 neonatal sera reduced the survival of Escherichia coli O7w:K1:NM to less than 20% of the original inoculum (P less than .03). Eleven neonatal sera did not kill the bacteria. Supplemental C9 (60 micrograms/ml) enhanced the bactericidal capacity of 10 neonatal sera. 125I-labeled C9 was deposited onto E. coli by neonatal sera, but less efficiently than by pooled adult sera. Supplemental IgG enhanced 125I-labeled C9 deposition and potentiated the bactericidal activity of exogenous C9. Therefore, neonatal sera contained diminished concentrations of C9 and killed E. coli inefficiently. In neonatal sera, supplemental C9 was deposited onto E. coli and enhanced bactericidal activity. These effects of C9 were potentiated by supplemental IgG.
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