Affiliation:
1. Departments of Pediatrics
2. Anatomy and Cell Biology
3. Pathology, University of Iowa, Carver College of Medicine, Iowa City, Iowa 52242
Abstract
ABSTRACT
The collectins surfactant-associated protein A (SP-A) and SP-D are components of innate immunity that are present before birth. Both proteins bind pathogens and assist in clearing infection. The significance of SP-A and SP-D as components of the neonatal immune system has not been investigated. To determine the role of SP-A and SP-D in neonatal immunity, wild-type, SP-A null, and SP-D null mice were bred in a bacterium-laden environment (corn dust bedding) or in a semisterile environment (cellulose fiber bedding). When reared in the corn dust bedding, SP-A null pups had significant mortality (
P
< 0.001) compared to both wild-type and SP-D null pups exposed to the same environment. The mortality of the SP-A null pups was associated with significant gastrointestinal tract pathology but little lung pathology. Moribund SP-A null newborn mice exhibited
Bacillus
sp. and
Enterococcus
sp. peritonitis. When the mother or newborn produced SP-A, newborn survival was significantly improved (
P
< 0.05) compared to the results when there was a complete absence of SP-A in both the mother and the pup. Significant sources of SP-A likely to protect a newborn include the neonatal lung and gastrointestinal tract but not the lactating mammary tissue of the mother. Furthermore, exogenous SP-A delivered by mouth to newborn SP-A null pups with SP-A null mothers improved newborn survival in the corn dust environment. Therefore, a lack of SP-D did not affect newborn survival, while SP-A produced by either the mother or the pup or oral exogenous SP-A significantly reduced newborn mortality associated with environmentally induced infection in SP-A null newborns.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Reference74 articles.
1. Adler, A., G. Gottesman, T. Dolfin, S. Arnon, R. Regev, S. Bauer, and I. Litmanovitz. 2005. Bacillus species sepsis in the neonatal intensive care unit. J. Infect.51:390-395.
2. Akiyama, J., A. Hoffman, C. Brown, L. Allen, J. Edmondson, F. Poulain, and S. Hawgood. 2002. Tissue distribution of surfactant proteins A and D in the mouse. J. Histochem. Cytochem.50:993-996.
3. Braun, J., and E. R. Stiehm. 1996. The B-lymphocyte system, p. 35-74. In E. R. Stiehm (ed.), Immunological disorders in infants and children, 4th ed. W. B. Saunders Co., Philadelphia, PA.
4. Borron, P. J., E. A. Mostaghel, C. Doyle, E. S. Walsh, M. G. McHeyzer-Williams, and J. R. Wright. 2002. Pulmonary surfactant proteins A and D directly suppress CD3+/CD4+ cell function: evidence for two shared mechanisms. J. Immunol.169:5844-5850.
5. Botas, C., F. Poulain, J. Akiyama, C. Brown, L. Allen, J. Goerke, J. Clements, E. Carlson, A. M. Gillespie, C. Epstein, and S. Hawgood. 1998. Altered surfactant homeostasis and alveolar type II cell morphology in mice lacking surfactant protein D. Proc. Natl. Acad. Sci. USA95:11869-11874.
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