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Definition of an optimal cytotoxic T lymphocyte epitope in the latently expressed Kaposi's sarcoma-associated herpesvirus kaposin protein.
Brander, C; O'Connor, P; Suscovich, T; Jones, N G; Lee, Y; Kedes, D; Ganem, D; Martin, J; Osmond, D; Southwood, S; Sette, A; Walker, B D; Scadden, D T.
Afiliación
  • Brander C; AIDS Research Center and Cancer Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
J Infect Dis ; 184(2): 119-26, 2001 Jul 15.
Article en En | MEDLINE | ID: mdl-11424007
ABSTRACT
Cytotoxic T lymphocytes (CTL) recognize and kill virus-infected cells and contribute to immunologic control of viral replication. For many herpesviruses (e.g., Epstein-Barr and cytomegalovirus), virus-specific CTL responses can be readily detected in infected persons, but CTL responses against Kaposi's sarcoma-associated herpesvirus (KSHV) appear to be weak and remain poorly characterized. Using a human leukocyte antigen (HLA) binding motif-based epitope prediction algorithm, we identified 37 HLA-A*0201 binding peptides from 8 KSHV open-reading frames (ORFs). After in vitro stimulation of peripheral blood mononuclear cells from KSHV-infected persons, CTL responses against 1 peptide in the KSHV kaposin protein (ORF K12) were detected in 2 HLA-A*0201-positive subjects. The optimal CTL epitope was identified by HLA restriction analysis and peptide titration assays. These data describe a latent phase viral gene product targeted by CTL that may be relevant for KSHV immunopathogenesis.
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Base de datos: MEDLINE Asunto principal: Proteínas Virales / Linfocitos T Citotóxicos / Antígenos HLA-A / Síndrome de Inmunodeficiencia Adquirida / Herpesvirus Humano 8 / Epítopos Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Infect Dis Año: 2001 Tipo del documento: Article
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Base de datos: MEDLINE Asunto principal: Proteínas Virales / Linfocitos T Citotóxicos / Antígenos HLA-A / Síndrome de Inmunodeficiencia Adquirida / Herpesvirus Humano 8 / Epítopos Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Infect Dis Año: 2001 Tipo del documento: Article