Azithromycin increases survival and reduces lung inflammation in cystic fibrosis mice
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作者:
Tsai, Wan C.
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Univ Michigan, Dept Pediat & Communicable Dis, Ann Arbor, MI 48105 USAUniv Michigan, Ann Arbor, MI 48109 USA
Tsai, Wan C.
[2
]
Hershenson, Marc B.
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Univ Michigan, Dept Pediat & Communicable Dis, Ann Arbor, MI 48105 USA
Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48105 USAUniv Michigan, Ann Arbor, MI 48109 USA
Hershenson, Marc B.
[2
,3
]
Zhou, Ying
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Univ Michigan, Dept Pediat & Communicable Dis, Ann Arbor, MI 48105 USAUniv Michigan, Ann Arbor, MI 48109 USA
Zhou, Ying
[2
]
Sajjan, Umadevi
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Univ Michigan, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Pediat & Communicable Dis, Ann Arbor, MI 48105 USAUniv Michigan, Ann Arbor, MI 48109 USA
Sajjan, Umadevi
[1
,2
]
机构:
[1] Univ Michigan, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Pediat & Communicable Dis, Ann Arbor, MI 48105 USA
[3] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48105 USA
Azithromycin (AZM) has been used as an anti-inflammatory agent in the treatment of cystic fibrosis (CF), particularly those with chronic infection with P. aeruginosa (PA). To investigate mechanisms associated with the beneficial effects of AZM in CF, we examined bacterial load, cytokine levels, and clearance of inflammatory cells in CF mice infected with mucoid PA and treated with AZM. Gut-corrected Cftr (tm1Unc) -TgN(FABPCFTR)#Jaw CF mice infected with an alginate-overproducing PA CF-isolate were treated with AZM or saline and examined for survival of animals, lung bacterial load, inflammation, cytokine levels, and apoptotic cells up to 5 days post-infection. Administration of AZM (20 mg/kg) 24 h after the infection improved 5-day survival to 95% compared with treatment with saline (56%). AZM administration was associated with significant reductions in bacterial load, decreased lung inflammation, and increased levels of IFN-gamma. AZM increased macrophage clearance of apoptotic neutrophils from the lung. Azithromycin enhances bacterial clearance and reduces lung inflammation by improving innate immune defense mechanisms in CF mice.
机构:
Mersin City Training & Res Hosp, Div Pediat Pulm, Clin Pediat, Mersin, TurkiyeMersin City Training & Res Hosp, Div Pediat Pulm, Clin Pediat, Mersin, Turkiye
Ozdemir, Ali
Ersoy, Murat
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Mersin City Training & Res Hosp, Clin Pediat, Mersin, TurkiyeMersin City Training & Res Hosp, Div Pediat Pulm, Clin Pediat, Mersin, Turkiye
机构:
Univ Milan, Dept Pathophysiol & Transplantat, Pediat Highly Intens Care Unit, Fdn IRCCS Ca Granda Osped Maggiore Policlin, I-20122 Milan, ItalyUniv Milan, Dept Pathophysiol & Transplantat, Pediat Highly Intens Care Unit, Fdn IRCCS Ca Granda Osped Maggiore Policlin, I-20122 Milan, Italy
Principi, N.
Blasi, F.
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Univ Milan, Dept Pathophysiol & Transplantat, Pneumol Unit, Fdn IRCCS Ca Granda Osped Maggiore Policlin, I-20122 Milan, ItalyUniv Milan, Dept Pathophysiol & Transplantat, Pediat Highly Intens Care Unit, Fdn IRCCS Ca Granda Osped Maggiore Policlin, I-20122 Milan, Italy
Blasi, F.
Esposito, S.
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机构:
Univ Milan, Dept Pathophysiol & Transplantat, Pediat Highly Intens Care Unit, Fdn IRCCS Ca Granda Osped Maggiore Policlin, I-20122 Milan, ItalyUniv Milan, Dept Pathophysiol & Transplantat, Pediat Highly Intens Care Unit, Fdn IRCCS Ca Granda Osped Maggiore Policlin, I-20122 Milan, Italy