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I类主要组织相容性复合体限制的细胞毒性T细胞所识别的I型人T细胞白血病病毒Tax蛋白中的靶表位

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.

作者信息

Kannagi M, Shida H, Igarashi H, Kuruma K, Murai H, Aono Y, Maruyama I, Osame M, Hattori T, Inoko H

机构信息

Department of Biodefence and Medical Virology, Kumamoto University Medical School, Japan.

出版信息

J Virol. 1992 May;66(5):2928-33. doi: 10.1128/JVI.66.5.2928-2933.1992.

Abstract

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 Sjögren 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.

摘要

人类I型T细胞白血病病毒(HTLV-I)的反式作用调节基因产物p40tax(Tax)是HTLV-I特异性细胞毒性T淋巴细胞(CTL)识别的主要靶抗原之一。本报告鉴定了Tax蛋白中的一个CTL表位。先前已证明,从两名患有HTLV-I相关脊髓病或干燥综合征的HTLV-I携带者建立的HTLV-I特异性CD8 + CTL系主要杀伤表达HTLV-I Tax的靶细胞。两名患者的CTL对用与Tax蛋白氨基末端序列相对应的24个氨基酸的合成肽脉冲处理的自体靶细胞表现出显著水平的细胞毒性。当靶细胞具有HLA-A2时,同种异体靶细胞也被该肽致敏以产生CTL。用表达Tax蛋白的痘苗病毒-HTLV-I重组体感染的靶细胞的细胞溶解检测到的Tax特异性细胞毒性几乎被用合成肽脉冲处理的竞争细胞完全抑制。这表明该肽中存在主要的CTL表位。使用较短肽的进一步分析表明,CTL表位的核心序列在第11至19位为LLFGYPVYV。该序列可与最近报道的HLA-A2特异性基序比对。

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