Infectious Disease Division, Department of Medicine, Perelman School of Medicine, Philadelphia, PA.
University Laboratory Animal Resources, Philadelphia, PA; Department of Pathobiology, School of Veterinary Medicine, Philadelphia, PA.
Transl Res. 2020 Jun;220:138-152. doi: 10.1016/j.trsl.2020.03.004. Epub 2020 Mar 16.
Genital herpes increases the risk of acquiring and transmitting Human Immunodeficiency Virus (HIV), is a source of anxiety for many about transmitting infection to intimate partners, and is life-threatening to newborns. A vaccine that prevents genital herpes infection is a high public health priority. An ideal vaccine will prevent both genital lesions and asymptomatic subclinical infection to reduce the risk of inadvertent transmission to partners, will be effective against genital herpes caused by herpes simplex virus types 1 and 2 (HSV-1, HSV-2), and will protect against neonatal herpes. Three phase 3 human trials were performed over the past 20 years that used HSV-2 glycoproteins essential for virus entry as immunogens. None achieved its primary endpoint, although each was partially successful in either delaying onset of infection or protecting a subset of female subjects that were HSV-1 and HSV-2 uninfected against HSV-1 genital infection. The success of future vaccine candidates may depend on improving the predictive value of animal models by requiring vaccines to achieve near-perfect protection in these models and by using the models to better define immune correlates of protection. Many vaccine candidates are under development, including DNA, modified mRNA, protein subunit, killed virus, and attenuated live virus vaccines. Lessons learned from prior vaccine studies and select candidate vaccines are discussed, including a trivalent nucleoside-modified mRNA vaccine that our laboratory is pursuing. We are optimistic that an effective vaccine for prevention of genital herpes will emerge in this decade.
生殖器疱疹会增加感染和传播人类免疫缺陷病毒(HIV)的风险,是许多人担心将感染传染给性伴侣的焦虑源,对新生儿也具有威胁生命的风险。预防生殖器疱疹感染的疫苗是一个高度的公共卫生重点。理想的疫苗将预防生殖器损伤和无症状的亚临床感染,以降低无意中传播给伴侣的风险,将对单纯疱疹病毒 1 型和 2 型(HSV-1、HSV-2)引起的生殖器疱疹有效,并将预防新生儿疱疹。在过去的 20 年中,进行了三项 3 期人体试验,使用了病毒进入所必需的 HSV-2 糖蛋白作为免疫原。没有一项达到其主要终点,尽管每一项都在一定程度上成功地延迟了感染的发作,或者保护了一部分 HSV-1 和 HSV-2 未感染的女性受试者免受 HSV-1 生殖器感染。未来疫苗候选物的成功可能取决于通过要求疫苗在这些模型中实现近乎完美的保护,并通过使用这些模型更好地定义保护的免疫相关性,来提高动物模型的预测价值。许多疫苗候选物正在开发中,包括 DNA、修饰的 mRNA、蛋白质亚单位、灭活病毒和减毒活病毒疫苗。讨论了从先前的疫苗研究和选定的候选疫苗中吸取的经验教训,包括我们实验室正在研究的三价核苷修饰的 mRNA 疫苗。我们乐观地认为,在这十年中,将出现一种预防生殖器疱疹的有效疫苗。