Marshall Neil A, Vickers Mark A, Barker Robert N
Department of Medicine and Therapeutics, University of Aberdeen, Foresterhill, Aberdeen, United Kingdom.
J Immunol. 2003 Jun 15;170(12):6183-9. doi: 10.4049/jimmunol.170.12.6183.
Viruses exploit a number of strategies to evade immune recognition. In this study, we describe a novel mechanism by which EBV, rather than avoiding detection, subverts the immune response by stimulating regulatory T cells that secrete IL-10. Human PBMC from all EBV-seropositive, but not -seronegative, donors responded to both purified latent membrane protein 1 and the corresponding immunodominant peptides with high levels of IL-10 secretion by CD4(+) T cells. These IL-10 responses, characteristic of T regulatory 1 cells, inhibited T cell proliferation and IFN-gamma secretion induced by both mitogen and recall Ag. It was confirmed that the inhibition was IL-10 dependent by the use of neutralizing Ab. The deviation of the immune response toward suppression is likely to be important in maintaining latency and EBV-associated tumors.
病毒利用多种策略来逃避免疫识别。在本研究中,我们描述了一种新机制,EB病毒并非避免被检测到,而是通过刺激分泌IL-10的调节性T细胞来颠覆免疫反应。来自所有EB病毒血清阳性而非血清阴性供体的人外周血单核细胞(PBMC),对纯化的潜伏膜蛋白1和相应的免疫显性肽均有反应,CD4(+) T细胞分泌高水平的IL-10。这些IL-10反应是调节性T1细胞的特征,抑制了有丝分裂原和回忆抗原诱导的T细胞增殖和IFN-γ分泌。通过使用中和抗体证实这种抑制是IL-10依赖性的。免疫反应向抑制方向的偏差可能在维持潜伏状态和EB病毒相关肿瘤方面起重要作用。