The effect of complement depletion on lung clearance of bacteria.
Open accessAbstract
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.”
From Trisomy 21 causes changes in the circulating proteome indicative of chronic autoinflammation (2017) · cites this paper as [69]
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Trisomy 21 causes changes in the circulating proteome indicative of chronic autoinflammation
Sullivan, K. D., Evans, D., Pandey, A., Hraha, T. H., Smith, K. P., Markham, N., Rachubinski, A. L., Wolter-Warmerdam, K., Hickey, F., Espinosa, J. M., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-13858-3 · Cited by 228 · see citing works
Sawai, T., Tomono, K., Yanagihara, K., Yamamoto, Y., Kaku, M., Hirakata, Y., Koga, H., Tashiro, T., & Kohno, S. (1997) · Infection and Immunity · doi:10.1128/iai.65.2.466-471.1997 · Cited by 97 · see citing works
- 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)
- PMC
- PMC371775
- 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
- bronze
- doi.org
- 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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