Abstract | BACKGROUND: METHODS: Mice were inoculated with parainfluenza type 1, Sendai Virus (SeV), and treated daily with PBS or azithromycin for 7 days post-inoculation. On day 8 and 21 we assessed airway inflammation in lung tissue, and quantified immune cells and inflammatory mediators in bronchoalveolar lavage (BAL). RESULTS: Compared to treatment with PBS, azithromycin significantly attenuated post-viral weight loss. During the peak of acute inflammation (day 8), azithromycin decreased total leukocyte accumulation in the lung tissue and BAL, with the largest fold-reduction in BAL neutrophils. This decreased inflammation was independent of changes in viral load. Azithromycin significantly attenuated the concentration of BAL inflammatory mediators and enhanced resolution of chronic airway inflammation evident by decreased BAL inflammatory mediators on day 21. CONCLUSIONS: In this mouse model of paramyxoviral bronchiolitis, azithromycin attenuated acute and chronic airway inflammation. These findings demonstrate anti-inflammatory effects of azithromycin that are not related to anti-viral activity. Our findings support the rationale for future prospective randomized clinical trials that will evaluate the effects of macrolides on acute viral bronchiolitis and their long-term consequences.
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Authors | Avraham Beigelman, Cassandra L Mikols, Sean P Gunsten, Carolyn L Cannon, Steven L Brody, Michael J Walter |
Journal | Respiratory research
(Respir Res)
Vol. 11
Pg. 90
(Jun 30 2010)
ISSN: 1465-993X [Electronic] England |
PMID | 20591166
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Anti-Inflammatory Agents
- Chemokines
- Cytokines
- Inflammation Mediators
- Azithromycin
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Topics |
- Animals
- Anti-Inflammatory Agents
(pharmacology)
- Azithromycin
(pharmacology)
- Bronchiolitis, Viral
(drug therapy, immunology, virology)
- Bronchoalveolar Lavage Fluid
(cytology, immunology)
- Chemokines
(metabolism)
- Cytokines
(metabolism)
- Disease Models, Animal
- Female
- Inflammation Mediators
(metabolism)
- Lung
(drug effects, immunology, virology)
- Mice
- Mice, Inbred C57BL
- Parainfluenza Virus 1, Human
(pathogenicity)
- Pneumonia
(immunology, prevention & control, virology)
- Respirovirus Infections
(drug therapy, immunology, virology)
- Sendai virus
(pathogenicity)
- Time Factors
- Viral Load
- Weight Loss
(drug effects)
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