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Complement function and the synthesis of lung surfactant may be a regulation which preterm infants have in common.
- Source :
-
Complement and inflammation [Complement Inflamm] 1991; Vol. 8 (5-6), pp. 320-7. - Publication Year :
- 1991
-
Abstract
- The levels of CH50, the complement components, C1q, C4, and C3, C3 degradation fragments, and factor B were determined in the cord blood of 128 newborn infants. The levels of C3, C4, and C3d3 (an index of chronic in vivo complement activation) were clearly lower in the 28 infants with respiratory distress syndrome (RDS) than in the infants with other lung diseases or with normal lungs. CH50 and factor B levels were also low in RDS. Levels of C1q and other serum components in RDS infants were similar to the average levels in other infants without RDS at a corresponding gestational age. Lung surfactant is synthesized in alveolar type 2 cells, in which the complement components C4, C3, and factor B, but not C1q, have been reported to be synthesized. It seems possible that common factors regulate the synthesis of some complement components and surfactant.
- Subjects :
- Complement C1q analysis
Complement C3 analysis
Complement C4 analysis
Complement Factor B analysis
Complement Hemolytic Activity Assay
Electrophoresis, Gel, Two-Dimensional
Fetal Blood chemistry
Humans
Immunoglobulin A analysis
Immunoglobulin G analysis
Immunoglobulin M analysis
Infant, Newborn
Infant, Small for Gestational Age immunology
Respiratory Distress Syndrome, Newborn diagnosis
Respiratory Distress Syndrome, Newborn immunology
Serum Albumin analysis
Complement System Proteins analysis
Fetal Organ Maturity
Infant, Premature immunology
Lung embryology
Pulmonary Surfactants biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1012-8204
- Volume :
- 8
- Issue :
- 5-6
- Database :
- MEDLINE
- Journal :
- Complement and inflammation
- Publication Type :
- Academic Journal
- Accession number :
- 1802550
- Full Text :
- https://doi.org/10.1159/000463203