TARGET EPITOPE IN THE TAX PROTEIN OF HUMAN T-CELL LEUKEMIA-VIRUS TYPE-I RECOGNIZED BY CLASS-I MAJOR HISTOCOMPATIBILITY COMPLEX-RESTRICTED CYTOTOXIC T-CELLS

被引:110
作者
KANNAGI, M
SHIDA, H
IGARASHI, H
KURUMA, K
MURAI, H
AONO, Y
MARUYAMA, I
OSAME, M
HATTORI, T
INOKO, H
HARADA, S
机构
[1] KUMAMOTO UNIV,SCH MED,DEPT INTERNAL MED 2,KUMAMOTO 860,JAPAN
[2] SHIONOGI INST MED SCI,OSAKA 566,JAPAN
[3] KAGOSHIMA UNIV,FAC MED,DEPT INTERNAL MED 3,KAGOSHIMA 890,JAPAN
[4] TOKAI UNIV,SCH MED,DEPT TRANSPLANTAT 2,ISEHARA,KANAGAWA 25911,JAPAN
关键词
D O I
10.1128/JVI.66.5.2928-2933.1992
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A trans-acting regulatory gene product p40tax (Tax) of human T-cell leukemia virus type I (HTLV-I) is one of the main target antigens recognized by cytotoxic T lymphocytes (CTL) specific for HTLV-I. A CTL epitope within the Tax protein was identified in this report. HTLV-I-specific CD8+ CTL lines established from two HTLV-I carriers with HTLV-I-associated myelopathy or Sjogren syndrome were previously demonstrated to kill predominantly the target cells expressing HTLV-I Tax. The CTL from two patients showed significant levels of cytotoxicity to autologous target cells pulsed with a synthetic peptide of 24 amino acids corresponding to the amino-terminal sequences of the Tax protein. Allogeneic target cells were also sensitized for CTL by this peptide when the target cells have HLA-A2. Tax-specific cytotoxicity, detected as cytolysis of the target cells infected with vaccinia virus-HTLV-I recombinant expressing Tax protein, was almost completely inhibited by competitor cells pulsed with the synthetic peptide. This indicates that a major CTL epitope is present in this peptide. Further analysis using shorter peptides revealed that the core sequence of the CTL epitope was LLFGYPVYV at positions 11 through 19. This sequence can be aligned with the HLA-A2-specific motifs reported recently.
引用
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页码:2928 / 2933
页数:6
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