Department of Pharmacy and Biotechnology, University of Bologna, I-40138 Bologna, Italy.
Viruses. 2019 Jul 18;11(7):659. doi: 10.3390/v11070659.
Parvovirus B19 (B19V) is a human pathogenic virus, responsible for an ample range of clinical manifestations. Infections are usually mild, self-limiting, and controlled by the development of a specific immune response, but in many cases clinical situations can be more complex and require therapy. Presently available treatments are only supportive, symptomatic, or unspecific, such as administration of intravenous immunoglobulins, and often of limited efficacy. The development of antiviral strategies against B19V should be considered of highest relevance for increasing the available options for more specific and effective therapeutic treatments. This field of research has been explored in recent years, registering some achievements as well as interesting future perspectives. In addition to immunoglobulins, some compounds have been shown to possess inhibitory activity against B19V. Hydroxyurea is an antiproliferative drug used in the treatment of sickle-cell disease that also possesses inhibitory activity against B19V. The nucleotide analogues Cidofovir and its lipid conjugate Brincidofovir are broad-range antivirals mostly active against dsDNA viruses, which showed an antiviral activity also against B19V. Newly synthesized coumarin derivatives offer possibilities for the development of molecules with antiviral activity. Identification of some flavonoid molecules, with direct inhibitory activity against the viral non-structural (NS) protein, indicates a possible line of development for direct antiviral agents. Continuing research in the field, leading to better knowledge of the viral lifecycle and a precise understanding of virus-cell interactions, will offer novel opportunities for developing more efficient, targeted antiviral agents, which can be translated into available therapeutic options.
细小病毒 B19(B19V)是一种人类致病病毒,可引起多种临床表现。感染通常为轻度、自限性,通过产生特异性免疫反应得到控制,但在许多情况下,临床情况可能更为复杂,需要治疗。目前的治疗方法仅为支持性、对症性或非特异性治疗,如静脉注射免疫球蛋白,且通常疗效有限。针对 B19V 的抗病毒策略的开发应被视为提高更具特异性和更有效治疗方法的重要选择。近年来,该研究领域取得了一些成果,也为未来提供了一些有趣的展望。除了免疫球蛋白,一些化合物已被证明具有抑制 B19V 的活性。羟基脲是一种用于治疗镰状细胞病的抗增殖药物,也具有抑制 B19V 的活性。核苷酸类似物 Cidofovir 及其脂质缀合物 Brincidofovir 是广谱抗病毒药物,主要对 dsDNA 病毒有效,对 B19V 也具有抗病毒活性。新合成的香豆素衍生物为具有抗病毒活性的分子的开发提供了可能性。一些黄酮类分子直接抑制病毒非结构(NS)蛋白的鉴定表明,直接抗病毒药物可能具有发展前景。持续的研究将有助于更好地了解病毒生命周期和病毒-细胞相互作用,为开发更有效、靶向性更强的抗病毒药物提供新的机会,这些药物可以转化为有效的治疗选择。