Christensen Neil D, Budgeon Lynn R
Departments of Pathology and Microbiology and Immunology, Penn State Hershey Medical Center, College of Medicine, Hershey, Pa., USA.
Curr Probl Dermatol. 2014;45:252-64. doi: 10.1159/000356183. Epub 2014 Mar 13.
Prophylactic and therapeutic immunization strategies are an effective method to control human papillomavirus (HPV)-associated diseases and cancers. Current protective virus-like particle and capsid-based vaccines are highly protective against vaccine-matched HPV types, and continued improvements in second-generation vaccines will lead to broader protection and cross-protection against the cancer-associated types. Increasing the effectiveness of broadly cross-protective L2-based immunogens will require adjuvants that activate innate immunity to thus enhance adaptive immunity. Therapeutic immunization strategies are needed to control and cure clinical disease and HPV-associated cancers. Significant advances in strategies to improve induction of cell-mediated immunity to HPV early (and capsid) proteins have been pretested in preclinical animal papillomavirus models. Several of these effective protocols have translated into successful therapeutic immune-mediated clearance of clinical lesions. Nevertheless, there are significant challenges in activating immunity to cancer-associated lesions due to various immune downregulatory events that are triggered by persistent HPV infections. A better understanding of immune responses to HPV lesions in situ is needed to optimize immune effector T cells that efficiently locate to sites of infection and which should lead to an effective immunotherapeutic management of this important human viral pathogen. The most effective immunization strategy may well require combination antiviral and immunotherapeutic treatments to achieve complete clearance of HPV infections and associated cancers.
预防性和治疗性免疫策略是控制人乳头瘤病毒(HPV)相关疾病和癌症的有效方法。目前基于保护性病毒样颗粒和衣壳的疫苗对疫苗匹配的HPV类型具有高度保护作用,第二代疫苗的持续改进将带来更广泛的保护以及对癌症相关类型的交叉保护。提高基于L2的广泛交叉保护免疫原的有效性将需要能够激活先天免疫从而增强适应性免疫的佐剂。需要治疗性免疫策略来控制和治愈临床疾病以及HPV相关癌症。在临床前动物乳头瘤病毒模型中已经对改善针对HPV早期(和衣壳)蛋白的细胞介导免疫诱导策略的重大进展进行了预测试。其中一些有效的方案已转化为成功的治疗性免疫介导的临床病变清除。然而,由于持续性HPV感染引发的各种免疫下调事件,在激活针对癌症相关病变的免疫方面仍存在重大挑战。需要更好地了解原位对HPV病变的免疫反应,以优化能够有效定位到感染部位的免疫效应T细胞,这应该会导致对这种重要的人类病毒病原体进行有效的免疫治疗管理。最有效的免疫策略很可能需要联合抗病毒和免疫治疗来实现HPV感染和相关癌症的完全清除。