| Journal of General Virology |
| First posted online 30 January 2002 | ARTICLE ABSTRACT |
| Rec 13 November 2001; Acc 17 January 2002 | DOI: 10.1099/vir.0.18224-0 |
Juan C. Ramírez, Esther Tapia and Mariano Esteban
Department of Molecular and Cellular Biology, Centro Nacional de Biotecnología, CSIC, Campus Universidad Autónoma, E-28049 Madrid, Spain
The WHO smallpox eradication program was concluded 21 years ago and the non-vaccinated population is now at risk of poxvirus infections, either by contact with monkeypox or through bioterrorism. Since drugs specific against poxvirus infections are limited, neutralizing monoclonal antibodies (mAbs) that are effective in vivo may be an important tool in controlling poxvirus infections. To this end, we studied the efficacy of the mAb C3, reactive against the trimeric 14-kDa protein of vaccinia virus (VV) localized in the membrane of the intracellular form of mature virus, for its ability to neutralize VV infection in mice. The results show that prophylactic as well as therapeutic administration of mAb C3 can be an effective means of control of VV replication within the host. The interval of antibody efficacy following a single administration, before and after VV inoculation, has been defined. This study reinforces the notion that neutralizing mAbs should be developed to control health-related human infections by poxviruses.
© 2002 SGM
This article is now available in the May 2002 print issue of JGV (vol. 83, 10591067). The complete issue of the journal may be seen in electronic form on JGV Online.