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FBL反应性CD8 + 细胞毒性T淋巴细胞和CD4 + 辅助性T淋巴细胞识别不同的Friend鼠白血病病毒编码抗原。

FBL-reactive CD8+ cytotoxic and CD4+ helper T lymphocytes recognize distinct Friend murine leukemia virus-encoded antigens.

作者信息

Klarnet J P, Kern D E, Okuno K, Holt C, Lilly F, Greenberg P D

机构信息

Department of Medicine, University of Washington, Seattle.

出版信息

J Exp Med. 1989 Feb 1;169(2):457-67. doi: 10.1084/jem.169.2.457.

Abstract

Immunization of C57BL/6 (B6) mice with FBL, a Friend murine leukemia virus (F-MuLV), induces both tumor-specific cytolytic CD8+ (CTL) and lymphokine-producing CD4+ Th that are effective in adoptive therapy of B6 mice bearing disseminated FBL leukemia. The current study evaluated the F-MuLV antigenic determinants expressed on FBL that are recognized by FBL-reactive CD8+ and CD4+ T cells. To identify the specificity of the FBL-reactive CD8+ CTL, Fisher rat embryo fibroblast (FRE) cells transfected with plasmids encoding F-MuLV gag or envelope (env) gene products plus the class I-restricting element Db were utilized. FBL-reactive CTL recognized FRE target cells transfected with the F-MuLV gag-encoded gene products, but failed to recognize targets expressing F-MuLV env. Attempts to generate env-specific CD8+ CTL by immunization with a recombinant vaccinia virus containing an inserted F-MuLV env gene were unsuccessful, despite the generation of a cytolytic response to vaccinia epitopes, implying that B6 mice fail to generate CD8+ CTL to env determinants. By contrast, CD4+ Th clones recognized FRE target cells transfected with env and not gag genes, and immunization with the recombinant vaccinia virus induced an env-specific CD4+ T cell response. These data show that in a Friend retrovirus-induced tumor model in which tumor rejection can be mediated by either CTL or Th, antigens derived from discrete retroviral proteins are predominantly responsible for activation of each T cell subset.

摘要

用弗氏鼠白血病病毒(F-MuLV)的FBL对C57BL/6(B6)小鼠进行免疫接种,可诱导产生肿瘤特异性细胞毒性CD8⁺(CTL)和产生淋巴因子的CD4⁺ Th细胞,这些细胞对患有播散性FBL白血病的B6小鼠的过继性治疗有效。本研究评估了FBL上表达的、能被FBL反应性CD8⁺和CD4⁺ T细胞识别的F-MuLV抗原决定簇。为了确定FBL反应性CD8⁺ CTL的特异性,使用了转染了编码F-MuLV gag或包膜(env)基因产物以及I类限制元件Db的质粒的Fisher大鼠胚胎成纤维细胞(FRE)。FBL反应性CTL识别转染了F-MuLV gag编码基因产物的FRE靶细胞,但不能识别表达F-MuLV env的靶细胞。尽管对痘苗抗原表位产生了细胞溶解反应,但用含有插入的F-MuLV env基因的重组痘苗病毒进行免疫接种来产生env特异性CD8⁺ CTL的尝试未成功,这意味着B6小鼠不能产生针对env决定簇的CD8⁺ CTL。相比之下,CD4⁺ Th克隆识别转染了env而非gag基因的FRE靶细胞,并且用重组痘苗病毒进行免疫接种诱导了env特异性CD4⁺ T细胞反应。这些数据表明,在一个Friend逆转录病毒诱导的肿瘤模型中,肿瘤排斥可由CTL或Th介导,来自离散逆转录病毒蛋白的抗原主要负责激活每个T细胞亚群。

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