Frazer I H
Department of Medicine, Princess, Alexandra Hospital, Woolloongabba, Queensland, Australia.
Genitourin Med. 1996 Dec;72(6):398-403. doi: 10.1136/sti.72.6.398.
Prophylactic vaccines for genital human papillomavirus (HPV) infection have been shown to be feasible in animal models, and suitable vaccine material based on virus-like particles can be produced in bulk at reasonable cost. Initiation of phase III clinical trials will follow definition of trial outcome measures through further epidemiological studies, and development of assays of host protective immunity. Vaccines could in principle eliminate HPV-related disease, as the human race is the only natural host for the relevant papillomaviruses (PVs). Therapeutic vaccines for genital HPV infection are also possible, but have not yet been demonstrated as feasible in practice because the choice of vaccine antigens is difficult, the method of their optimal delivery is uncertain, and the nature of the relevant antiviral immunity is unknown. PV species specificity will require trials to be conducted in man, which will slow definition of an ideal vaccine.
用于预防生殖器人乳头瘤病毒(HPV)感染的疫苗在动物模型中已被证明是可行的,基于病毒样颗粒的合适疫苗材料能够以合理成本大量生产。通过进一步的流行病学研究确定试验结果测量指标并开发宿主保护性免疫检测方法之后,将启动III期临床试验。原则上疫苗可以消除HPV相关疾病,因为人类是相关乳头瘤病毒(PV)的唯一自然宿主。用于治疗生殖器HPV感染的疫苗也是有可能的,但由于疫苗抗原的选择困难、最佳递送方法不确定以及相关抗病毒免疫的性质未知,目前尚未在实践中证明其可行性。PV的种属特异性将需要在人体中进行试验,这将延缓理想疫苗的确定。