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Published online ahead of print on 4 March 2009 as doi:10.1099/vir.0.009308-0
Journal of General Virology 2009;90:1119.

A more recent version of this article appeared on May 1, 2009 J Gen Virol (2009), DOI 10.1099/vir.0.009308-0
© 2009 Society for General Microbiology

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Treatment with respiratory syncytial virus G glycoprotein monoclonal antibody or F(ab')2 components mediate reduced pulmonary inflammation in mice

Congrong Miao1, Gertrud U. Radu1, Hayat Caidi1, Ralph A. Tripp2, Larry J. Anderson1 and Lia M. Haynes1,3

1 Centers for Disease Control and Prevention;
2 University of Georgia

3 E-mail: loh5{at}cdc.gov

Therapeutic treatment with a non-neutralizing monoclonal antibody (131-2G) specific to respiratory syncytial virus (RSV) G glycoprotein mediates virus clearance and decreased leukocyte trafficking and interferon gamma (IFN-{gamma}) production in the lungs of RSV-infected mice. Its F(ab')2 component only mediates decreased leukocyte trafficking and IFN-{gamma} production without reducing virus replication. Thus, this monoclonal antibody has two independent actions that could facilitate treatment and/or prevention of RSV infection by both reducing virus replication and virus induced pulmonary inflammation.

Received 1 December 2008; accepted 26 January 2009.


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E. J. Collarini, F. E.-H. Lee, O. Foord, M. Park, G. Sperinde, H. Wu, W. D. Harriman, S. F. Carroll, S. L. Ellsworth, L. J. Anderson, et al.
Potent High-Affinity Antibodies for Treatment and Prophylaxis of Respiratory Syncytial Virus Derived from B Cells of Infected Patients
J. Immunol., November 15, 2009; 183(10): 6338 - 6345.
[Abstract] [Full Text] [PDF]




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