|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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-
) production in the lungs of RSV-infected mice. Its F(ab')2 component only mediates decreased leukocyte trafficking and IFN-
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.
This article has been cited by other articles:
![]() |
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] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |