Carter L L, Murphy K M
Department of Pathology and Center for Immunology, Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Exp Med. 1999 Apr 19;189(8):1355-60. doi: 10.1084/jem.189.8.1355.
CD4(+) and CD8(+) T cells exhibit important differences in their major effector functions. CD8(+) T cells provide protection against pathogens through cytolytic activity, whereas CD4(+) T cells exert important regulatory activity through production of cytokines. However, both lineages can produce interferon (IFN)-gamma, which can contribute to protective immunity. Here we show that CD4(+) and CD8(+) T cells differ in their regulation of IFN-gamma production. Both lineages require signal transducer and activator of transcription (Stat)4 activation for IFN-gamma induced by interleukin (IL)-12/IL-18 signaling, but only CD4(+) T cells require Stat4 for IFN-gamma induction via the TCR pathway. In response to antigen, CD8(+) T cells can produce IFN-gamma independently of IL-12, whereas CD4(+) T cells require IL-12 and Stat4 activation. Thus, there is a lineage-specific requirement for Stat4 activation in antigen-induced IFN-gamma production based on differences in TCR signaling between CD4(+) and CD8(+) T cells.
CD4(+)和CD8(+) T细胞在其主要效应功能上表现出重要差异。CD8(+) T细胞通过细胞溶解活性提供针对病原体的保护,而CD4(+) T细胞则通过产生细胞因子发挥重要的调节活性。然而,这两个谱系都能产生干扰素(IFN)-γ,其可有助于保护性免疫。在此我们表明,CD4(+)和CD8(+) T细胞在IFN-γ产生的调节方面存在差异。两个谱系对于白介素(IL)-12/IL-18信号诱导的IFN-γ都需要信号转导子和转录激活子(Stat)4激活,但只有CD4(+) T细胞通过TCR途径诱导IFN-γ时需要Stat4。响应抗原时,CD8(+) T细胞可独立于IL-12产生IFN-γ,而CD4(+) T细胞则需要IL-12和Stat4激活。因此,基于CD4(+)和CD8(+) T细胞之间TCR信号的差异,在抗原诱导的IFN-γ产生中对Stat4激活存在谱系特异性需求。