Fisher Randall, Darrow David H, Tranter Margene, Williams Judith V
Department of Pediatrics, Eastern Virginia Medical School, VA, USA.
Curr Opin Pediatr. 2008 Aug;20(4):441-5. doi: 10.1097/MOP.0b013e328305e298.
The human papillomavirus vaccine is now Food and Drug Administration-approved for girls and young women ages 9-26 years and Advisory Committee on Immunization Practices-recommended for girls ages 11-12 years of age. Several issues have shrouded its debut and continue to provide controversy that may hinder effective delivery of this vaccine to young people in industrialized as well as third world countries.
The quadrivalent and divalent vaccines are compared, particularly with respect to juvenile recurrent respiratory papillomatosis. Recommendations for administration are summarized. Immunization of men and cost effectiveness are discussed. Issues regarding compulsory vaccination and attitudes of parents about human papillomavirus vaccination are reviewed.
Studies of the human papillomavirus vaccine are very promising, showing excellent efficacy and very few adverse events. It remains to be determined if it will be licensed in the United States for use in boys and men. Some stumbling blocks to implementing the vaccine in the United States need to be addressed in order to gain widespread acceptance.
人乳头瘤病毒疫苗现已获美国食品药品管理局批准,可用于9至26岁的女孩和年轻女性,免疫实践咨询委员会也建议对11至12岁的女孩接种该疫苗。该疫苗首次亮相后便出现了若干问题,且争议不断,这可能会妨碍在工业化国家和第三世界国家向年轻人有效推广这种疫苗。
对四价和二价疫苗进行了比较,尤其在青少年复发性呼吸道乳头瘤病方面。总结了疫苗接种的建议。讨论了男性接种疫苗及成本效益问题。审视了强制接种疫苗的相关问题以及家长对人乳头瘤病毒疫苗接种的态度。
人乳头瘤病毒疫苗的研究前景十分广阔,显示出卓越的疗效且不良反应极少。该疫苗在美国是否会获批用于男孩和男性还有待确定。为了获得广泛认可,需要解决在美国推广该疫苗时遇到的一些障碍。