Wang F, Blaese R M, Zoon K C, Tosato G
J Clin Invest. 1987 Jan;79(1):7-14. doi: 10.1172/JCI112810.
Suppression and/or cytotoxicity are believed to play an important role in the defense against Epstein-Barr virus (EBV) infection. To analyze the role of suppressor T cells in relation to EBV, we sought to clone and study these T cells. Analysis of 152 T cell clones derived from the peripheral blood of two patients with acute EBV-induced infectious mononucleosis (IM) yielded 11 highly suppressive clones that had no cytotoxic activity for the natural killer sensitive K562 cell line, an autologous EBV-infected cell line, or an allogeneic EBV-infected B cell line. Four of six suppressor T cell clones also profoundly inhibited EBV-induced immunoglobulin production, and five of five clones delayed the outgrowth of immortalized cells. These results indicate that during acute IM, suppressor T cells capable of inhibiting B cell activation in the absence of cytotoxicity can be identified, and may play a key role in the control of EBV infection.
抑制作用和/或细胞毒性被认为在抵御爱泼斯坦-巴尔病毒(EBV)感染中发挥重要作用。为了分析抑制性T细胞与EBV相关的作用,我们试图克隆并研究这些T细胞。对来自两名急性EBV诱导的传染性单核细胞增多症(IM)患者外周血的152个T细胞克隆进行分析,得到了11个高度抑制性克隆,这些克隆对自然杀伤敏感的K562细胞系、自体EBV感染的细胞系或同种异体EBV感染的B细胞系均无细胞毒性活性。六个抑制性T细胞克隆中的四个也显著抑制了EBV诱导的免疫球蛋白产生,五个克隆中的五个延迟了永生化细胞的生长。这些结果表明,在急性IM期间,可以鉴定出在无细胞毒性情况下能够抑制B细胞活化的抑制性T细胞,并且它们可能在控制EBV感染中起关键作用。