Landais Elise, Saulquin Xavier, Houssaint Elisabeth
INSERM U463, Institut de Biologie, Nantes, France.
Int J Dev Biol. 2005;49(2-3):285-92. doi: 10.1387/ijdb.041947el.
The Epstein-Barr virus (EBV) is a gamma-herpes virus which establishes latent, life-long infection in more than 95% of the human adult population. Despite its growth transforming capacity, most carriers control EBV associated malignacies efficiently and remain free of EBV+ tumors. Though EBV is controlled by a potent immune response, this virus uses latency to persist in vivo. This review summarizes work which has been done to characterize T cell responses to EBV. The CD8 T cell responses are rather well characterized and have been shown by several groups to be highly focused towards early lytic antigens. Much less is known about CD4 T cell epitopes, due to the small size of the CD4 compartment. However, recent data indicate a control of lytic and latent cycles of EBV by specific CD4+ T cells. A clear understanding of the T cell response to EBV is important with a view to developing immunotherapies for the virus and its related malignancies.
爱泼斯坦-巴尔病毒(EBV)是一种γ疱疹病毒,在超过95%的成年人群中建立潜伏性的终身感染。尽管它具有生长转化能力,但大多数携带者能有效地控制与EBV相关的恶性肿瘤,并且不会患上EBV阳性肿瘤。虽然EBV受强大的免疫反应控制,但这种病毒利用潜伏状态在体内持续存在。这篇综述总结了为表征T细胞对EBV的反应所做的工作。CD8 T细胞反应的特征较为明确,多个研究小组已表明其高度集中于早期裂解抗原。由于CD4细胞区室较小,关于CD4 T细胞表位的了解要少得多。然而,最近的数据表明特定的CD4+ T细胞可控制EBV的裂解和潜伏周期。鉴于要开发针对该病毒及其相关恶性肿瘤的免疫疗法,清楚了解T细胞对EBV的反应很重要。