TY - JOUR
T1 - Characterization of HLA-A2.1-restricted epitopes, conserved in both Hantaan and Sin Nombre viruses, in Hantaan virus-infected patients
AU - Lee, Ki Young
AU - Chun, Eunyoung
AU - Kim, Na Yeon
AU - Seong, Baik L.
PY - 2002
Y1 - 2002
N2 - Nine different CTL epitopes, conserved in both Hantaan virus (HTNV) and Sin Nombre virus (SNV), were selected for study. The binding affinity of each peptide with HLA-A2.1 molecules in vitro was determined and antigen-specific responses from seven donors who had a previous field infection with HTNV were examined. Although the strength or frequency of CTL activity showed different patterns in the seven patients, five of seven patients showed significant activity against at least one or more epitope peptides. In particular, the peptide ILQDMRNTI (HTNV, aa 334-342; SNV, aa 333-341), which elicited CTL activity in five patients, was shown to be specifically HLA-A2. 1-restricted in partially cloned CD8+ T cells and also induced activated and effector CD8+ T cell-producing T cytotoxic (Tc) type 1 cytokines, such as IL-2 and IFN-γ. The results suggest that this epitope would serve as a useful component for the intervention of both HTNV and SNV infection.
AB - Nine different CTL epitopes, conserved in both Hantaan virus (HTNV) and Sin Nombre virus (SNV), were selected for study. The binding affinity of each peptide with HLA-A2.1 molecules in vitro was determined and antigen-specific responses from seven donors who had a previous field infection with HTNV were examined. Although the strength or frequency of CTL activity showed different patterns in the seven patients, five of seven patients showed significant activity against at least one or more epitope peptides. In particular, the peptide ILQDMRNTI (HTNV, aa 334-342; SNV, aa 333-341), which elicited CTL activity in five patients, was shown to be specifically HLA-A2. 1-restricted in partially cloned CD8+ T cells and also induced activated and effector CD8+ T cell-producing T cytotoxic (Tc) type 1 cytokines, such as IL-2 and IFN-γ. The results suggest that this epitope would serve as a useful component for the intervention of both HTNV and SNV infection.
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U2 - 10.1099/0022-1317-83-5-1131
DO - 10.1099/0022-1317-83-5-1131
M3 - Article
C2 - 11961268
AN - SCOPUS:0036247158
SN - 0022-1317
VL - 83
SP - 1131
EP - 1136
JO - Journal of General Virology
JF - Journal of General Virology
IS - 5
ER -