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Short Communication |
1 Department of Pediatrics, University of Texas Medical Branch, Galveston, TX, USA
2 Microbiotix Inc., Worcester, MA, USA
3 Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA
4 Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX, USA
Correspondence
Antonella Casola
ancasola{at}utmb.edu
BALB/c mice infected with human metapneumovirus (hMPV) were treated with the sulfated sialyl lipid NMSO3 (one dose of 50 mg kg–1) given at the time of infection. NMSO3 significantly reduced viral replication in the lungs, as well as hMPV-induced body weight loss, pulmonary inflammation and cytokine production, suggesting that antiviral treatment initiated at the beginning of viral infection can modify hMPV-induced disease.
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