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宫颈癌的预防性和治疗性疫苗

Preventative and therapeutic vaccines for cervical cancer.

作者信息

Roden Richard, Wu T-C

机构信息

Department of Pathology, The Johns Hopkins Medical Institutions, 512H Ross Building, 720 Rutland Avenue, Baltimore, MD 21205, USA.

出版信息

Expert Rev Vaccines. 2003 Aug;2(4):495-516. doi: 10.1586/14760584.2.4.495.

Abstract

"High-risk" genotypes of the human papillomavirus (HPV), most commonly HPV genotype 16, are the primary etiologic agents of cervical cancer. Indeed HPV DNA is detected in 99% of cervical carcinomas. Thus, cervical cancer and other HPV-associated malignancies might be prevented or treated by the induction of the appropriate viral-antigen-specific immune responses. Transmission of papillomavirus may be prevented by the generation of antibodies to capsid proteins L1 and L2 that neutralize viral infection. HPV L1 virus-like particles (VLPs) show great promise as prophylactic HPV vaccines in ongoing clinical trials but L2-based preventative vaccines have yet to be tested in patients. Since the capsid proteins are not expressed at detectable levels by infected basal keratinocytes or in HPV-transformed cells, therapeutic vaccines generally target the nonstructural early viral antigens. Two HPV oncogenic proteins, E6 and E7, are critical to the induction and maintenance of cellular transformation and are co-expressed in the majority of HPV-containing carcinomas. Although other early viral antigens show promise for vaccination against papillomas, therapeutic vaccines targeting E6 and E7 may provide the best opportunity to control HPV-associated malignancies. Various candidate therapeutic HPV vaccines are currently being tested whereby E6 and/or E7 are administered in live vectors, as peptides or proteins, in nucleic acid form, as components of chimeric VLPs, or in cell-based vaccines. Encouraging results from experimental vaccination systems in animal models have led to several prophylactic and therapeutic vaccine clinical trials. Should this new generation of HPV preventative and therapeutic vaccines function in patients as demonstrated in animal models, oncogenic HPV infection and its associated malignancies could be controlled by vaccination. Importantly, recent advances in HPV detection and continued improvements in screening further enhance our opportunities to systematically eradicate HPV-associated malignancy.

摘要

人乳头瘤病毒(HPV)的“高危”基因型,最常见的是HPV 16型,是宫颈癌的主要病因。事实上,在99%的宫颈癌中都能检测到HPV DNA。因此,通过诱导适当的病毒抗原特异性免疫反应,宫颈癌和其他HPV相关恶性肿瘤可能得以预防或治疗。针对衣壳蛋白L1和L2产生的中和病毒感染的抗体可预防乳头瘤病毒传播。HPV L1病毒样颗粒(VLP)在正在进行的临床试验中作为预防性HPV疫苗显示出巨大潜力,但基于L2的预防性疫苗尚未在患者中进行测试。由于感染的基底角质形成细胞或HPV转化细胞中衣壳蛋白的表达水平无法检测到,治疗性疫苗通常靶向非结构性早期病毒抗原。两种HPV致癌蛋白E6和E7对于细胞转化的诱导和维持至关重要,并且在大多数含HPV的癌中共同表达。尽管其他早期病毒抗原在针对乳头瘤的疫苗接种方面显示出潜力,但靶向E6和E7的治疗性疫苗可能提供控制HPV相关恶性肿瘤的最佳机会。目前正在测试各种候选治疗性HPV疫苗,其中E6和/或E7以活载体、肽或蛋白质、核酸形式、嵌合VLP的成分或基于细胞的疫苗的形式给药。动物模型实验性疫苗接种系统取得的令人鼓舞的结果已促成多项预防性和治疗性疫苗临床试验。如果新一代HPV预防性和治疗性疫苗在患者中能像在动物模型中那样发挥作用,致癌性HPV感染及其相关恶性肿瘤就可以通过接种疫苗得到控制。重要的是,HPV检测的最新进展以及筛查的持续改进进一步增加了我们系统性根除HPV相关恶性肿瘤的机会。

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