@article{mbs:/content/journal/jgv/10.1099/0022-1317-70-5-1173, author = "Stokes*, Anne and Allen, G. P. and Pullen, L. A. and Murray, P. Keith", title = "A Hamster Model of Equine Herpesvirus Type 1 (EHV-1) Infection; Passive Protection by Monoclonal Antibodies to EHV-1 Glycoproteins 13, 14 and 17/18", journal= "Journal of General Virology", year = "1989", volume = "70", number = "5", pages = "1173-1183", doi = "https://doi.org/10.1099/0022-1317-70-5-1173", url = "https://www.microbiologyresearch.org/content/journal/jgv/10.1099/0022-1317-70-5-1173", publisher = "Microbiology Society", issn = "1465-2099", type = "Journal Article", keywords = "glycoproteins", keywords = "hamster model", keywords = "EHV-1", abstract = "Summary Following intraperitoneal or intranasal inoculation of the Syrian hamster with equine herpesvirus type 1 (EHV-1), strain Kentucky D, virus replicated in the liver and lungs reaching a peak at 4 days post-infection (p.i.). By day 6 p.i. virus titres in these organs had reduced and the spleen contained virus-specific cytotoxic cells. This cytotoxicity was mediated by T cells since treatment of effector cells with a monoclonal antibody to hamster T lymphocytes inhibited the effect. An antiviral humoral immune response was present by day 4 when antibodies capable of lysing EHV-1-infected target cells in the presence of complement were detected. The transfer of serum from recovered hamsters into naive recipients 24 h before challenge prevented virus infection, whereas serum transferred 24 h after challenge reduced the titre of virus recovered from target organs. Inoculation of hamsters with monoclonal antibodies directed to glycoproteins 13, 14 and 17/18 of a subtype 1 virus (Army 183) before virus challenge protected hamsters. This hamster model will prove useful for studying the immune response to EHV-1 and evaluating the immunogenicity of individual virus components.", }