Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Wisconsin 53711, USA.
Braz J Infect Dis. 2009 Aug;13(4):304-10. doi: 10.1590/s1413-86702009000400013.
The road to the discovery of a vaccine for HIV has been arduous and will continue to be difficult over the ensuing twenty years. Most vaccines are developed by inducing neutralizing antibodies against the target pathogen or by using attenuated strains of the particular pathogen to engender a variety of protective immune responses. Unfortunately, simple methods of generating anti-HIV antibodies have already failed in a phase III clinical trial. While attenuated SIV variants work well against homologous challenges in non-human primates, the potential for reversion to a more pathogenic virus and recombination with challenge viruses will preclude the use of attenuated HIV in the field. It has been exceedingly frustrating to vaccinate for HIV-specific neutralizing antibodies given the enormous diversity of the Envelope (Env) glycoprotein and its well-developed glycan shield. However, there are several antibodies that will neutralize many different strains of HIV and inducing these types of antibodies in vaccinees remains the goal of a vigorous effort to develop a vaccine for HIV based on neutralizing antibodies. Given the difficulty in generating broadly reactive neutralizing antibodies, the HIV vaccine field has turned its attention to inducing T cell responses against the virus using a variety of vectors. Unfortunately, the results from Merck's phase IIb STEP trial proved to be disappointing. Vaccinees received Adenovirus type 5 (Ad5) expressing Gag, Pol, and Nef of HIV. This vaccine regimen failed to either prevent infection or reduce the level of HIV replication after challenge. These results mirrored those in non-human primate testing of Ad5 using rigorous SIV challenge models. This review will focus on recent developments in HIV vaccine development. We will deal largely with attempts to develop a T cell-based vaccine using the non-human primate SIV challenge model.
发现 HIV 疫苗的道路是艰难的,在接下来的二十年里仍将充满困难。大多数疫苗是通过诱导针对目标病原体的中和抗体或使用病原体的减毒株来产生各种保护性免疫反应来开发的。不幸的是,产生抗 HIV 抗体的简单方法已经在 III 期临床试验中失败了。虽然减毒 SIV 变体在非人类灵长类动物中对同源性挑战效果很好,但潜在的返祖为更具致病性的病毒和与挑战病毒的重组将排除在现场使用减毒 HIV。鉴于包膜 (Env) 糖蛋白的巨大多样性及其高度发达的聚糖屏蔽,针对 HIV 特异性中和抗体进行疫苗接种令人非常沮丧。然而,有几种抗体可以中和许多不同株的 HIV,诱导疫苗接种者产生这些类型的抗体仍然是基于中和抗体开发 HIV 疫苗的积极努力的目标。鉴于产生广泛反应性中和抗体的困难,HIV 疫苗领域已将注意力转向使用各种载体诱导针对病毒的 T 细胞反应。不幸的是,默克公司的 IIb 期 STEP 试验的结果令人失望。接种者接受了表达 HIV 的 Gag、Pol 和 Nef 的腺病毒 5 (Ad5)。这种疫苗方案既不能预防感染,也不能在挑战后降低 HIV 复制水平。这些结果与使用严格的 SIV 挑战模型对 Ad5 进行的非人类灵长类动物测试结果相吻合。本综述将重点介绍 HIV 疫苗开发的最新进展。我们将主要讨论使用非人类灵长类动物 SIV 挑战模型开发基于 T 细胞的疫苗的尝试。