National AIDS Center, Istituto Superiore di Sanità, V.le Regina Elena 299, 00161, Rome, Italy.
Adv Exp Med Biol. 2009;655:189-242. doi: 10.1007/978-1-4419-1132-2_14.
The acquired immunodeficiency syndrome (AIDS) emerged in the human population in the summer of 1981. According to the latest United Nations estimates, worldwide over 33 million people are infected with human immunodeficiency virus (HIV) and the prevalence rates continue to rise globally. To control the alarming spread of HIV, an urgent need exists for developing a safe and effective vaccine that prevents individuals from becoming infected or progressing to disease. To be effective, an HIV/AIDS vaccine should induce broad and long-lasting humoral and cellular immune responses, at both mucosal and systemic level. However, the nature of protective immune responses remains largely elusive and this represents one of the major roadblocks preventing the development of an effective vaccine. Here we summarize our present understanding of the factors responsible for resistance to infection or control of progression to disease in human and monkey that may be relevant to vaccine development and briefly review recent approaches which are currently being tested in clinical trials. Finally, the rationale and the current status of novel strategies based on nonstructural HIV-1 proteins, such as Tat, Nef and Rev, used alone or in combination with modified structural HIV-1 Env proteins are discussed.
获得性免疫缺陷综合征(AIDS)于 1981 年夏天出现在人类群体中。根据联合国的最新估计,全世界有超过 3300 万人感染了人类免疫缺陷病毒(HIV),全球的流行率仍在继续上升。为了控制 HIV 的惊人传播,迫切需要开发一种安全有效的疫苗,以防止个人感染或发展为疾病。为了有效,HIV/AIDS 疫苗应诱导广泛和持久的体液和细胞免疫反应,在粘膜和全身水平上。然而,保护性免疫反应的性质在很大程度上仍难以捉摸,这是阻止有效疫苗开发的主要障碍之一。在这里,我们总结了我们目前对人类和猴子感染抵抗或疾病进展控制的因素的理解,这些因素可能与疫苗开发有关,并简要回顾了目前正在临床试验中测试的最新方法。最后,讨论了基于 HIV-1 非结构蛋白(如 Tat、Nef 和 Rev)的新型策略的原理和现状,这些策略单独或与修饰的 HIV-1 Env 蛋白联合使用。