期刊
JOURNAL OF VIROLOGY
卷 84, 期 18, 页码 9632-9636出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.00451-10
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资金
- National Institutes of Health [5RO1AI06275-03]
- U.S. Department of Energy
- CDC
- Georgia Research Alliance
We examined whether prophylactically administered anti-respiratory syncytial virus (anti-RSV) G monoclonal antibody (MAb) would decrease the pulmonary inflammation associated with primary RSV infection and formalin-inactivated RSV (FI-RSV)-enhanced disease in mice. MAb 131-2G administration 1 day prior to primary infection reduced the pulmonary inflammatory response and the level of RSV replication. Further, intact or F(ab')(2) forms of MAb 131-2G administered 1 day prior to infection in FI-RSV-vaccinated mice reduced enhanced inflammation and disease. This study shows that an anti-RSV G protein MAb might provide prophylaxis against both primary infection and FI-RSV-associated enhanced disease. It is possible that antibodies with similar reactivities might prevent enhanced disease and improve the safety of nonlive virus vaccines.
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