Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, 1600 Clifton Rd. NE, Mailstop G-18, Atlanta, GA 30333, USA.
J Virol. 2010 Sep;84(18):9632-6. doi: 10.1128/JVI.00451-10. Epub 2010 Jun 30.
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.
我们研究了预防性给予抗呼吸道合胞病毒(抗 RSV)G 单克隆抗体(MAb)是否会减少原发性 RSV 感染和甲醛灭活 RSV(FI-RSV)增强疾病小鼠的肺部炎症。MAb 131-2G 在原发性感染前 1 天给药可降低肺部炎症反应和 RSV 复制水平。此外,在 FI-RSV 疫苗接种小鼠中,感染前 1 天给予完整或 F(ab')(2)形式的 MAb 131-2G 可减少增强的炎症和疾病。这项研究表明,抗 RSV G 蛋白 MAb 可能提供针对原发性感染和 FI-RSV 相关增强疾病的预防。具有类似反应性的抗体可能预防增强疾病并提高非活病毒疫苗的安全性。