de la Torre Juan C
Immunology and Microbial Science, IMM-6, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Antiviral Res. 2008 Dec;80(3):239-50. doi: 10.1016/j.antiviral.2008.08.002. Epub 2008 Sep 7.
Several arenaviruses cause hemorrhagic fever (HF) in humans, and evidence indicates that the worldwide-distributed prototypic arenavirus lymphocytic choriomeningitis virus (LCMV) is a neglected human pathogen of clinical significance. Moreover, arenaviruses pose a biodefense threat. No licensed anti-arenavirus vaccines are available, and current anti-arenavirus therapy is limited to the use of ribavirin, which is only partially effective and is associated with anemia and other side effects. Therefore, it is important to develop effective vaccines and better antiviral drugs to combat the dual threats of naturally occurring and intentionally introduced arenavirus infections. The development of arenavirus reverse genetic systems is allowing investigators to conduct a detailed molecular characterization of the viral cis-acting signals and trans-acting factors that control each of the steps of the arenavirus life cycle, including RNA synthesis, packaging and budding. Knowledge derived from these studies is uncovering potential novel targets for therapeutic intervention, as well as facilitating the establishment of assays to identify and characterize candidate antiviral drugs capable of interfering with specific steps of the virus life cycle. Likewise, the ability to generate predetermined specific mutations within the arenavirus genome and analyze their phenotypic expression would significantly contribute to the elucidation of arenavirus-host interactions, including the basis of their ability to cause severe HF. This, in turn, could lead to the development of novel, potent and safe arenavirus vaccines.
几种沙粒病毒可导致人类出血热(HF),有证据表明,全球分布的原型沙粒病毒淋巴细胞性脉络丛脑膜炎病毒(LCMV)是一种被忽视但具有临床意义的人类病原体。此外,沙粒病毒构成生物防御威胁。目前尚无获得许可的抗沙粒病毒疫苗,当前的抗沙粒病毒治疗仅限于使用利巴韦林,其效果有限且会导致贫血和其他副作用。因此,开发有效的疫苗和更好的抗病毒药物以应对自然发生和人为引入的沙粒病毒感染的双重威胁非常重要。沙粒病毒反向遗传系统的开发使研究人员能够对控制沙粒病毒生命周期各个步骤(包括RNA合成、包装和出芽)的病毒顺式作用信号和反式作用因子进行详细的分子表征。从这些研究中获得的知识正在揭示治疗干预的潜在新靶点,并有助于建立用于鉴定和表征能够干扰病毒生命周期特定步骤的候选抗病毒药物的检测方法。同样,在沙粒病毒基因组内产生预定特定突变并分析其表型表达的能力将显著有助于阐明沙粒病毒与宿主的相互作用,包括它们导致严重出血热的能力基础。这反过来可能会导致开发新型、高效且安全的沙粒病毒疫苗。