| Literature DB >> 11483773 |
E J Usherwood1, K A Ward, M A Blackman, J P Stewart, D L Woodland.
Abstract
Vaccines that can reduce the load of latent gammaherpesvirus infections are eagerly sought. One attractive strategy is vaccination against latency-associated proteins, which may increase the efficiency with which T cells recognize and eliminate latently infected cells. However, due to the lack of tractable animal model systems, the effect of latent-antigen vaccination on gammaherpesvirus latency is not known. Here we use the murine gammaherpesvirus model to investigate the impact of vaccination with the latency-associated M2 antigen. As expected, vaccination had no effect on the acute lung infection. However, there was a significant reduction in the load of latently infected cells in the initial stages of the latent infection, when M2 is expressed. These data show for the first time that latent-antigen vaccination can reduce the level of latency in vivo and suggest that vaccination strategies involving other latent antigens may ultimately be successfully used to reduce the long-term latent infection.Entities:
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Year: 2001 PMID: 11483773 PMCID: PMC115072 DOI: 10.1128/jvi.75.17.8283-8288.2001
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103