Research Centre for Biomedical Sciences, Sunway University, Bandar Sunway, Selangor 47500, Malaysia.
Department of Surgery, Faculty of Medicine, University of Malaya, Jalan Universiti, Kuala Lumpur, 50603, Malaysia.
Int J Med Sci. 2017 Oct 15;14(13):1342-1359. doi: 10.7150/ijms.21875. eCollection 2017.
Dengue is an important global threat caused by dengue virus (DENV) that records an estimated 390 million infections annually. Despite the availability of CYD-TDV as a commercial vaccine, its long-term efficacy against all four dengue virus serotypes remains unsatisfactory. There is therefore an urgent need for the development of antiviral drugs for the treatment of dengue. Peptide was once a neglected choice of medical treatment but it has lately regained interest from the pharmaceutical industry following pioneering advancements in technology. In this review, the design of peptide drugs, antiviral activities and mechanisms of peptides and peptidomimetics (modified peptides) action against dengue virus are discussed. The development of peptides as inhibitors for viral entry, replication and translation is also described, with a focus on the three main targets, namely, the host cell receptors, viral structural proteins and viral non-structural proteins. The antiviral peptides designed based on these approaches may lead to the discovery of novel anti-DENV therapeutics that can treat dengue patients.
登革热是一种由登革病毒(DENV)引起的重要全球威胁,据估计每年有 3.9 亿人感染。尽管有 CYD-TDV 作为商业疫苗,但它对所有四种登革热病毒血清型的长期疗效仍不尽如人意。因此,迫切需要开发抗病毒药物来治疗登革热。肽曾经是一种被忽视的治疗选择,但最近随着技术的开创性进展,制药行业重新对其产生了兴趣。在这篇综述中,讨论了肽药物的设计、肽和拟肽(修饰肽)的抗病毒活性和作用机制以及针对登革热病毒的抗病毒肽作为病毒进入、复制和翻译抑制剂的开发,重点介绍了三个主要靶点,即宿主细胞受体、病毒结构蛋白和病毒非结构蛋白。基于这些方法设计的抗病毒肽可能会发现新的抗 DENV 治疗方法,从而治疗登革热患者。