Cited by 117Complement system in diseasesPneumonia and Respiratory InfectionsImmunodeficiency and Autoimmune Disorders

The effect of complement depletion on lung clearance of bacteria.

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Gross, G N, Rehm, S R, Pierce, A K·1978·Journal of Clinical Investigation

Abstract

We have investigated the effect of hypocomplementemia on early pulmonary clearance of four species of bacteria. The experiments were performed in an inbred animal model to minimize immunologic variability. Complement was depleted by cobra venom factor, and activity in serum was monitored with a phagocytic assay. Bacterial specific antibodies were examined by an indirect radioimmunoassay, and animals with high levels of activity were excluded from anaysis. 4 h after aerosolization with Streptococcus pneumoniae, complement-depleted animals had cleared only 75% of the initial number of organisms, whereas saline-treated controls cleared 91% (P less than 0.01). Aerosolization with Pseudomonas aeruginosa was followed at 4 h by a twofold greater growth of organisms in the complement-depleted animals (446% of original deposition) as compared to the saline-treated controls (211% of original deposition) (P less than 0.02). Clearance of Klebsiella pneumoniae and Staphylococcus aureus were similar in complement-depleted animals and saline-treated controls. These experiments suggest that hypocomplementemia predisposes to bacterial pneumonia and may explain the high incidence of pulmonary infections in patients having impaired complement activity. Our results further indicate that varying defense mechanisms may be involved with clearing the lung of differing bacterial species.

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  • Hypocomplementia could contribute to the increased risk of bacterial lung pneumonia and otitis media in Down syndrome, as complement depletion prevents proper clearance of Streptococcus pneumoniae.

    “Hypocomplementia could clearly contribute to the observed increased risk of bacterial lung pneumonia and otitis media in the population with DS68, as complement depletion prevents proper clearance of Streptococcus pneumoniae 69.”

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Research works printed but not linked: 4

  1. Winkelstein, J. A., M. R. Smith, and H. S. Shin. 1975. The role of C3 as an opsonin in the early stages of infec- tion. Proc. Soc. Exp. Biol. Med. 149: 397-401.
  2. Wilks, S. S. 1962. Mathematical Statistics. R. A. Bradley, J. S. Hunter, D. G. Kendall, G. S. Wilson, editors. John Wiley & Sons, Inc., New York.
  3. Springer, G. F., and R. E. Horton. 1969. Blood group isoantibody stimulation in man by feeding blood group- active bacteria. J. Clin. Invest. 48: 1280-1291.
  4. Loosli, C. G., and R. F. Baker. 1962. Acute experimental pneumococcal (Type I) pneumonia in the mouse: the migration of leukocytes from the pulmonary capillaries into the alveolar spaces as revealed by the electron microscope. Trans. Am. Clin. Climatol. Assoc. 74: 15-28.

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Authors
Gross, G. N., Rehm, S. R., & Pierce, A. K.
Affiliations
The University of Texas Southwestern Medical Center (US)
Venue
Journal of Clinical Investigation
Published
1978-08-01
Volume
62
Issue
2
Pages
373-378
ISSN
0021-9738 (ISSN-L)
OpenAlex
W1979423093
Cited by
117
References
0
Citations by year
2025: 1 · 2024: 1 · 2023: 2 · 2022: 2 · 2021: 1 · 2020: 2 · 2019: 1 · 2018: 2 · 2017: 1 · 2016: 2 · 2015: 2 · 2014: 3 · 2013: 1 · 2012: 2
FWCI
1.99
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Investigation (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
Louisiana Board of Regents
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Complement system in diseases
  • Health Sciences › Medicine › Epidemiology › Pneumonia and Respiratory Infections
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
Keywords
complement depletion, hypocomplementemia, bacterial pneumonia, Streptococcus pneumoniae, Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, cobra venom factor, aerosolized bacteria, complement system
MeSH terms
Animals, Antibodies, Bacterial, Bacteria, Complement System Proteins, Elapid Venoms, Female, Immunity, Innate, Klebsiella pneumoniae, Lung, Mice, Inbred BALB C, Pseudomonas aeruginosa, Staphylococcus aureus, Streptococcus pneumoniae, Mice

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