Laboratory of Molecular Immunology, The Rockefeller University, New York, New York, USA.
J Virol. 2013 Aug;87(15):8535-44. doi: 10.1128/JVI.00868-13. Epub 2013 May 29.
The development of an effective vaccine preventing HIV-1 infection remains elusive. Thus, the development of novel approaches capable of preventing HIV-1 transmission is of paramount importance. However, this is partly hindered by the lack of an easily accessible small-animal model to rapidly measure viral entry. Here, we report the generation of a human CD4- and human CCR5-expressing transgenic luciferase reporter mouse that facilitates measurement of peritoneal and genitomucosal HIV-1 pseudovirus entry in vivo. We show that antibodies and antiretrovirals mediate preexposure protection in this mouse model and that the serum antibody concentration required for protection from cervicovaginal infection is comparable to that required to protect macaques. Our results suggest that this system represents a model for the preclinical evaluation of prophylactic or vaccine candidates. It further supports the idea that broadly neutralizing antibodies should be evaluated for use as preexposure prophylaxis in clinical trials.
开发一种有效的预防 HIV-1 感染的疫苗仍然难以实现。因此,开发能够预防 HIV-1 传播的新方法至关重要。然而,这在一定程度上受到缺乏易于获得的小动物模型来快速测量病毒进入的阻碍。在这里,我们报告了一种人 CD4 和人 CCR5 表达的荧光素酶报告基因转基因小鼠的产生,该小鼠有助于测量体内腹膜和生殖黏膜 HIV-1 假病毒的进入。我们表明,抗体和抗逆转录病毒药物在这种小鼠模型中介导了暴露前保护,并且保护生殖道感染所需的血清抗体浓度与保护猕猴所需的浓度相当。我们的结果表明,该系统代表了预防性或候选疫苗的临床前评估模型。它进一步支持了广泛中和抗体应该作为暴露前预防在临床试验中进行评估的观点。