C. Brander et al., Definition of an optimal cytotoxic T lymphocyte epitope in the latently expressed Kaposi's sarcoma-associated herpesvirus kaposin protein, J INFEC DIS, 184(2), 2001, pp. 119-126
Cytotoxic T lymphocytes (CTL) recognize and kill virus-infected cells and c
ontribute to immunologic control of viral replication. For many herpesvirus
es (e.g., Epstein-Barr and cytomegalovirus), virus-specific CTL responses c
an be readily detected in infected persons, but CTL responses against Kapos
i's sarcoma-associated herpesvirus (KSHV) appear to be weak and remain poor
ly 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 peri
pheral blood mononuclear cells from KSHV-infected persons, CTL responses ag
ainst 1 peptide in the KSHV kaposin protein (ORF K12) were detected in 2 HL
A-A*0201-positive subjects. The optimal CTL epitope was identified by HLA r
estriction analysis and peptide titration assays. These data describe a lat
ent phase viral gene product targeted by CTL that may be relevant for KSHV
immunopathogenesis.