Journal of Virology · 2000 · 42 citations · 37 references
Life SciencesImmunologyInfectious DiseasesMolecular VirologyVaccine ImmunologyVaccinologyAntigen RecognitionCell-mediated ImmunityCellular Immunity In InfectionVaccine Antigen DiscoveryViral InfectionsViral VaccinesCd4 Positive T Cell ResponsesCd4 Positive T CellsCd4 T Cell ActivationCd4+ T Helper Cell ResponsesHerpes Simplex Virus VaccinesT-cell EpitopesVaccine Candidate AntigensViral-specific Cytotoxic T Lymphocyte Responses
We used CD4 lymphocyte clones from herpes simplex virus type 2 (HSV-2) lesions or the cervix and molecular libraries of HSV-2 DNA to define HSV-2 major capsid protein VP5 and glycoprotein E (gE) as T-cell antigens. Responses to eight HSV-2 glycoprotein, tegument, nonstructural, or capsid antigens were compared in 19 donors. Recognition of VP5 and tegument VP22 were similar to that of gB2 and gD2, currently under study as vaccines. These prevalence data suggest that HSV capsid and tegument proteins may also be candidate vaccine antigens.
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The Genome Sequence of Herpes Simplex Virus Type 2
Aidan Dolan, Fiona E. Jamieson, Charles Cunningham et al. · Journal of Virology · 1998 · 358 citations · Full text