Kuwano K, Kawashima T, Arai S
Department of Microbiology, Kurume University School of Medicine, Fukuoka, Japan.
Viral Immunol. 1993 Spring;6(1):1-11. doi: 10.1089/vim.1993.6.1.
We observed that an influenza-specific cytotoxic T lymphocyte (CTL) clone (B7B7) stimulated with peptide-antigen could produce TNF-alpha and IFN-gamma simultaneously. The culture supernatant containing both TNF-alpha and IFN-gamma of antigen-stimulated CTL clone B7B7 significantly enhanced the lysis of influenza A/PR/8 virus-infected L-M2d6 cells or Meth A cells. Enhanced lysis of influenza virus-infected cells by the supernatants was inhibited by pretreatment of the supernatant with antimurine TNF-alpha antibody and antimurine IFN-gamma antibody. In addition to a single CTL clone, we observed that bulk-cultured CTLs were able to produce TNF and IFN when incubated with target cells. These results suggest that the protective mechanism mediated by TNF-alpha and IFN-gamma secreted from CTL may be possible in the course of an influenza infection.
我们观察到,用肽抗原刺激的流感特异性细胞毒性T淋巴细胞(CTL)克隆(B7B7)可同时产生肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)。抗原刺激的CTL克隆B7B7中同时含有TNF-α和IFN-γ的培养上清液可显著增强甲型流感病毒/PR/8感染的L-M2d6细胞或Meth A细胞的裂解。用抗鼠TNF-α抗体和抗鼠IFN-γ抗体预处理上清液可抑制上清液对流感病毒感染细胞的增强裂解作用。除单个CTL克隆外,我们还观察到,大量培养的CTL与靶细胞孵育时能够产生TNF和IFN。这些结果表明,在流感感染过程中,CTL分泌的TNF-α和IFN-γ介导的保护机制可能发挥作用。