Lowy Douglas R
J Clin Invest. 2016 Jan;126(1):5-11. doi: 10.1172/JCI85446. Epub 2016 Jan 4.
Identification of HPV infection as the etiologic agent of virtually all cases of cervical cancer, as well as a proportion of other epithelial cancers, has led to development of three FDA-approved multivalent prophylactic HPV vaccines composed of virus-like particles (VLPs). This essay describes the research and development that led to the VLP vaccines; discusses their safety, efficacy, and short-term effect on HPV-associated disease; and speculates that even a single dose of these vaccines, when given to adolescents, might be able to confer long-term protection. The HPV field exemplifies how long-term funding for basic research has lead to clinical interventions with the long-term potential to eradicate most cancers attributable to HPV infection. Although this essay is the result of my receiving the 2015 Harrington Prize for Innovation in Medicine from the Harrington Discovery Institute and the American Society for Clinical Investigation, this clinical advance has depended on the research of many investigators, development of commercial vaccines by the pharmaceutical companies, and participation of many patient volunteers in the clinical trials.
几乎所有宫颈癌病例以及部分其他上皮癌病例的病因均为HPV感染,这一发现促使美国食品药品监督管理局(FDA)批准了三种由病毒样颗粒(VLP)组成的多价预防性HPV疫苗。本文描述了促成VLP疫苗的研发过程;讨论了它们的安全性、有效性以及对HPV相关疾病的短期影响;并推测,这些疫苗即使仅给青少年接种一剂,也可能提供长期保护。HPV领域例证了对基础研究的长期资助如何带来具有长期潜力根除大多数由HPV感染引起癌症的临床干预措施。尽管本文是我获得哈林顿发现研究所和美国临床研究学会颁发的2015年哈林顿医学创新奖的成果,但这一临床进展依赖于众多研究人员的研究、制药公司对商业疫苗的开发以及许多患者志愿者参与临床试验。