Antiviral therapies: advances and perspectives

被引:44
作者
Goncalves, Bruna Carolina [1 ]
Lopes Barbosa, Mario Gabriel [1 ]
Silva Olak, Anna Paula [1 ]
Belebecha Terezo, Natalia [1 ]
Nishi, Leticia [2 ]
Watanabe, Maria Angelica [2 ]
Marinello, Poliana [2 ]
Zendrini Rechenchoski, Daniele [1 ]
Dejato Rocha, Sergio Paulo [1 ]
Faccin-Galhardi, Ligia Carla [1 ]
机构
[1] Univ Estadual Londrina, Ctr Ciencias Biol, Dept Microbiol, BR-86057970 Londrina, Parana, Brazil
[2] Univ Estadual Londrina, Ctr Ciencias Biol, Dept Ciencias Patol, BR-86057970 Londrina, Parana, Brazil
关键词
antivirals; CRISPR‐ Cas; monoclonal antibodies; nanoparticles; IN-VITRO; MONOCLONAL-ANTIBODIES; VIRUS-REPLICATION; VIRAL-INFECTIONS; SPIKE PROTEIN; ZIKA VIRUS; NANOPARTICLES; RNA; EPIDEMIOLOGY; SARS-COV-2;
D O I
10.1111/fcp.12609
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Viral infections cause high morbidity and mortality, threaten public health, and impose a socioeconomic burden. We have seen the recent emergence of SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2), the causative agent of COVID-19 that has already infected more than 29 million people, with more than 900 000 deaths since its identification in December 2019. Considering the significant impact of viral infections, research and development of new antivirals and control strategies are essential. In this paper, we summarize 96 antivirals approved by the Food and Drug Administration between 1987 and 2019. Of these, 49 (51%) are used in treatments against human immunodeficiency virus (HIV), four against human papillomavirus, six against cytomegalovirus, eight against hepatitis B virus, five against influenza, six against herpes simplex virus, 17 against hepatitis C virus and one against respiratory syncytial virus. This review also describes future perspectives for new antiviral therapies such as nanotechnologies, monoclonal antibodies and the CRISPR-Cas system. These strategies are suggested as inhibitors of viral replication by various means, such as direct binding to the viral particle, blocking the infection, changes in intracellular mechanisms or viral genes, preventing replication and virion formation. We also observed that a large number of viral agents have no therapy available and the majority of those approved in the last 32 years are restricted to some groups, especially anti-HIV. Additionally, the emergence of new viruses and strains resistant to available antivirals has necessitated the formulation of new antivirals.
引用
收藏
页码:305 / 320
页数:16
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