Center for Vaccine Research, Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Viruses. 2013 Dec 2;5(12):2963-76. doi: 10.3390/v5122963.
Equine infectious anemia (EIA), identified in 1843 [1] as an infectious disease of horses and as a viral infection in 1904, remains a concern in veterinary medicine today. Equine infectious anemia virus (EIAV) has served as an animal model of HIV-1/AIDS research since the original identification of HIV. Similar to other lentiviruses, EIAV has a high propensity for genomic sequence and antigenic variation, principally in its envelope (Env) proteins. However, EIAV possesses a unique and dynamic disease presentation that has facilitated comprehensive analyses of the interactions between the evolving virus population, progressive host immune responses, and the definition of viral and host correlates of immune control and vaccine efficacy. Summarized here are key findings in EIAV that have provided important lessons toward understanding long term immune control of lentivirus infections and the parameters for development of an enduring broadly protective AIDS vaccine.
马传染性贫血(EIA)于 1843 年[1]被确定为一种马的传染病,并于 1904 年被确定为一种病毒感染,至今仍是兽医领域关注的问题。自 HIV 首次被发现以来,马传染性贫血病毒(EIAV)一直作为 HIV-1/AIDS 研究的动物模型。与其他慢病毒一样,EIAV 具有高度的基因组序列和抗原变异性,主要在其包膜(Env)蛋白中。然而,EIAV 具有独特而动态的疾病表现,这有助于对不断进化的病毒群体、宿主渐进性免疫反应以及病毒和宿主免疫控制和疫苗效力相关因素之间的相互作用进行全面分析。本文总结了 EIAV 的重要发现,这些发现为理解慢病毒感染的长期免疫控制以及开发持久、广泛保护的艾滋病疫苗的参数提供了重要的经验教训。