Khanna Rajiv, Moss Denis, Gandhi Maher
Tumour Immunology Laboratory, Queensland Institute of Medical Research, Queensland, Australia.
Nat Clin Pract Oncol. 2005 Mar;2(3):138-49. doi: 10.1038/ncponc0107.
The Epstein-Barr virus (EBV) is uniquely associated with a broad range of human malignancies. In spite of their diverse cellular origin, most of these malignancies share common features, including the expression of either some or all of the EBV latent proteins, which can be potentially exploited for immune-based therapies. Here we discuss new and emerging strategies to manipulate the immune response to specifically boost T-cell immunity towards viral proteins that are expressed in EBV-associated malignancies. These strategies are used either alone or as an adjuvant therapy in combination with chemotherapy and/or monoclonal antibodies. Overall, this strategy may serve as a new paradigm for the successful multi-modality treatment of malignancies.
爱泼斯坦-巴尔病毒(EBV)与多种人类恶性肿瘤有着独特的关联。尽管这些恶性肿瘤的细胞起源各不相同,但其中大多数都具有共同特征,包括表达部分或全部EBV潜伏蛋白,这些蛋白有可能被用于基于免疫的治疗。在此,我们讨论一些新出现的策略,这些策略可调控免疫反应,以特异性增强针对EBV相关恶性肿瘤中表达的病毒蛋白的T细胞免疫。这些策略可单独使用,也可作为辅助疗法与化疗和/或单克隆抗体联合使用。总体而言,这一策略可能成为成功多模式治疗恶性肿瘤的新范例。