Enssle K H, Fleischer B
Department of Medical Microbiology and Immunology, University of Ulm, West Germany.
Clin Exp Immunol. 1990 Mar;79(3):409-15. doi: 10.1111/j.1365-2249.1990.tb08104.x.
Cytotoxic T lymphocytes (CTL) with the CD4+ phenotype that recognize major histocompatibility complex (MHC) class II antigens are detectable very frequently in cultures of human alloreactive or virus-specific T cells. The significance of these CD4+ CTL for an immune reaction in vivo is not clear. Since Epstein-Barr virus (EBV) transformed B cells express HLA-class I and class II antigens equally well both CD8+ and CD4+ CTL should be stimulated during an acute EBV infection. We analysed the MHC specificity and the phenotype of EBV-specific CTL from patients with infectious mononucleosis (IM). When tested directly without any previous culture, T cells from patients in the acute phase of IM showed specific MHC-restricted cytotoxicity against the autologous B cell line. Addition of a HLA class I specific monoclonal antibody (MoAb) but not of a HLA class II specific MoAb resulted in a complete blocking of the lytic activity. Cell sorting revealed that the entire cytotoxic activity was present in the CD8+ fraction whereas no specific CTL were detectable in the CD4+ fraction. The absence of cytotoxicity in CD4+ cells was not due to a lack of activation of these cells since both CD8+ and CD4+ cells were activated in situ, showing spontaneous growth in interleukin-2 (IL-2) and expressing the activation marker TP103. Frequency estimation revealed that 1/300-1/600 CD8+ but only 1/2000-1/4000 CD4+ T cells gave rise to a specific CTL colony after 10 days. If CD4+ colonies were tested repeatedly for cytotoxicity we found that CD4+ CTL acquired their cytotoxicity during in vitro culture. In addition, we isolated EBV-specific CD4+ T cell clones able to lyse their stimulator cells in the presence but not in the absence of lectin, even after a long period of culture. Taken together our results show that cytotoxicity mediated by CD4+ T cells does not play a role in an anti-viral immune response.
在人类同种异体反应性或病毒特异性T细胞培养物中,经常可检测到具有识别主要组织相容性复合体(MHC)Ⅱ类抗原的CD4⁺表型的细胞毒性T淋巴细胞(CTL)。这些CD4⁺CTL在体内免疫反应中的意义尚不清楚。由于爱泼斯坦-巴尔病毒(EBV)转化的B细胞能同等良好地表达HLA-Ⅰ类和Ⅱ类抗原,在急性EBV感染期间,CD8⁺和CD4⁺CTL均应受到刺激。我们分析了传染性单核细胞增多症(IM)患者中EBV特异性CTL的MHC特异性和表型。当直接检测而不进行任何预先培养时,处于IM急性期患者的T细胞对自体B细胞系表现出特异性MHC限制性细胞毒性。添加HLA-Ⅰ类特异性单克隆抗体(MoAb)而非HLA-Ⅱ类特异性MoAb可导致裂解活性完全阻断。细胞分选显示,整个细胞毒性活性存在于CD8⁺组分中,而在CD4⁺组分中未检测到特异性CTL。CD4⁺细胞中缺乏细胞毒性并非由于这些细胞未被激活,因为CD8⁺和CD4⁺细胞在原位均被激活,在白细胞介素-2(IL-2)中表现出自发性生长并表达激活标志物TP103。频率估计显示,1/300 - 1/600的CD8⁺T细胞,但只有1/2000 - 1/4000的CD4⁺T细胞在10天后产生特异性CTL集落。如果对CD4⁺集落反复进行细胞毒性测试,我们发现CD4⁺CTL在体外培养期间获得了它们的细胞毒性。此外,我们分离出了EBV特异性CD4⁺T细胞克隆,即使经过长时间培养,这些克隆在有凝集素存在但无凝集素时不存在的情况下能够裂解其刺激细胞。综上所述,我们的结果表明,CD4⁺T细胞介导的细胞毒性在抗病毒免疫反应中不起作用。