Surman Sherri L, Sealy Robert, Jones Bart G, Hurwitz Julia L
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Hum Vaccin. 2009 Apr;5(4):268-71. doi: 10.4161/hv.5.4.7706.
In the fall of 2007, the HIV-1 research field received news that their front-runner vaccine was not protective. In response to this disappointment, scientists are now reviewing the intricacies of the immune response toward HIV-1 to develop new and better strategies for vaccine development. Decades ago, researchers recognized the impressive amino acid and carbohydrate diversity of HIV-1, and the associated obstacles to vaccine development. At first glance, the diversity and other unique features of HIV-1 may seem insurmountable, but attention to vaccine successes in other fields serves to renew optimism. The newly-licensed rotavirus and papillomavirus cocktail vaccines remind scientists that diverse pathogens can be conquered and that the chronic nature of a virus infection need not thwart successful vaccine design. Here we describe current efforts to gain insights from other vaccine fields and to adopt a cocktail vaccine approach for the prevention of HIV-1 infections in humans.
2007年秋,HIV-1研究领域收到消息,其领先的疫苗并无保护作用。面对这一令人失望的结果,科学家们正在重新审视针对HIV-1的免疫反应的复杂性,以制定新的、更好的疫苗研发策略。几十年前,研究人员就认识到HIV-1令人印象深刻的氨基酸和碳水化合物多样性,以及由此带来的疫苗研发障碍。乍一看,HIV-1的多样性和其他独特特征似乎难以克服,但关注其他领域疫苗的成功案例有助于重拾乐观情绪。新获批的轮状病毒和乳头瘤病毒联合疫苗提醒科学家,多种病原体是可以被征服的,病毒感染的慢性特性未必会阻碍成功的疫苗设计。在此,我们描述了目前从其他疫苗领域获取见解并采用联合疫苗方法预防人类HIV-1感染的努力。