Department of Clinical Oncology, Building 1, K1-P, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands.
Curr Opin Immunol. 2011 Apr;23(2):252-7. doi: 10.1016/j.coi.2010.12.010. Epub 2011 Jan 13.
Human Papilloma Virus (HPV)-induced (pre-)malignancies offer an excellent case for the rational design of immunotherapeutic strategies against cancer. Transformed cells express tumor-specific antigens of viral origin while the spontaneous antitumor response and the immunological make up of HPV-induced tumors do not differ from other immunogenic epithelial tumors. A first clinically active therapeutic HPV vaccine has been developed and clear links were found between the type and kinetics of vaccine-induced T-cell immunity. Here, we will review the mechanisms determining the success and failure of therapeutic vaccines against HPV-induced tumors, with particular emphasis on the immunological setting in which these vaccines need to work. The recent progress in therapeutic HPV vaccination will guide the development of successful vaccines in other diseases.
人乳头瘤病毒(HPV)诱导的(前)恶性肿瘤为针对癌症的合理设计免疫治疗策略提供了一个极好的案例。转化细胞表达病毒来源的肿瘤特异性抗原,而自发性抗肿瘤反应和 HPV 诱导肿瘤的免疫组成与其他免疫原性上皮肿瘤没有区别。已经开发出第一种临床有效的治疗性 HPV 疫苗,并且在疫苗诱导的 T 细胞免疫的类型和动力学之间发现了明确的联系。在这里,我们将回顾决定治疗性 HPV 肿瘤疫苗成败的机制,特别强调这些疫苗需要发挥作用的免疫环境。治疗性 HPV 疫苗接种的最新进展将指导其他疾病中成功疫苗的开发。