Chemistry and Biotechnology Institute, Federal University of Alagoas, Maceio, Brazil.
Curr Med Chem. 2021;28(15):2887-2942. doi: 10.2174/0929867327666200812215852.
Viral diseases are responsible for several deaths around the world. Over the past few years, the world has seen several outbreaks caused by viral diseases that, for a long time, seemed to possess no risk. These are diseases that have been forgotten for a long time and, until nowadays, there are no approved drugs or vaccines, leading the pharmaceutical industry and several research groups to run out of time in the search for new pharmacological treatments or prevention methods. In this context, drug repurposing proves to be a fast and economically viable technique, considering the fact that it uses drugs that have a well-established safety profile. Thus, in this review, we present the main advances in drug repurposing and their benefit for searching new treatments against emerging viral diseases.
We conducted a search in the bibliographic databases (Science Direct, Bentham Science, PubMed, Springer, ACS Publisher, Wiley, and NIH's COVID-19 Portfolio) using the keywords "drug repurposing", "emerging viral infections" and each of the diseases reported here (CoV; ZIKV; DENV; CHIKV; EBOV and MARV) as an inclusion/exclusion criterion. A subjective analysis was performed regarding the quality of the works for inclusion in this manuscript. Thus, the selected works were those that presented drugs repositioned against the emerging viral diseases presented here by means of computational, high-throughput screening or phenotype-based strategies, with no time limit and of relevant scientific value.
291 papers were selected, 24 of which were CHIKV; 52 for ZIKV; 43 for DENV; 35 for EBOV; 10 for MARV; and 56 for CoV and the rest (72 papers) related to the drugs repurposing and emerging viral diseases. Among CoV-related articles, most were published in 2020 (31 papers), updating the current topic. Besides, between the years 2003 - 2005, 10 articles were created, and from 2011 - 2015, there were 7 articles, portraying the outbreaks that occurred at that time. For ZIKV, similar to CoV, most publications were during the period of outbreaks between the years 2016 - 2017 (23 articles). Similarly, most CHIKV (13 papers) and DENV (14 papers) publications occur at the same time interval. For EBOV (13 papers) and MARV (4 papers), they were between the years 2015 - 2016. Through this review, several drugs were highlighted that can be evolved in vivo and clinical trials as possible used against these pathogens showed that remdesivir represent potential treatments against CoV. Furthermore, ribavirin may also be a potential treatment against CHIKV; sofosbuvir against ZIKV; celgosivir against DENV, and favipiravir against EBOV and MARV, representing new hopes against these pathogens.
The conclusions of this review manuscript show the potential of the drug repurposing strategy in the discovery of new pharmaceutical products, as from this approach, drugs could be used against emerging viral diseases. Thus, this strategy deserves more attention among research groups and is a promising approach to the discovery of new drugs against emerging viral diseases and also other diseases.
病毒疾病是导致全球死亡的主要原因之一。在过去的几年中,全球爆发了数起因长期以来似乎没有风险的病毒疾病引起的疫情。这些疾病已经被遗忘了很长时间,而且直到现在,还没有批准的药物或疫苗,这使得制药行业和几个研究小组在寻找新的药理学治疗方法或预防方法方面时间紧迫。在这种情况下,药物再利用被证明是一种快速且经济可行的技术,因为它使用了具有良好安全性的药物。因此,在这篇综述中,我们介绍了药物再利用的主要进展及其在寻找新的治疗方法以应对新兴病毒性疾病方面的益处。
我们使用关键词“药物再利用”、“新兴病毒感染”以及本文中报道的每种疾病(CoV;ZIKV;DENV;CHIKV;EBOV 和 MARV)在文献数据库(Science Direct、Bentham Science、PubMed、Springer、ACS 出版商、Wiley 和 NIH 的 COVID-19 投资组合)中进行了搜索。对纳入本手稿的作品进行了主观质量分析。因此,选择的作品是通过计算、高通量筛选或基于表型的策略重新定位用于治疗本文中报道的新兴病毒疾病的药物,没有时间限制且具有重要的科学价值。
共筛选出 291 篇论文,其中 24 篇与 CHIKV 相关;52 篇与 ZIKV 相关;43 篇与 DENV 相关;35 篇与 EBOV 相关;10 篇与 MARV 相关;56 篇与 CoV 相关,其余(72 篇)与药物再利用和新兴病毒疾病相关。与 CoV 相关的文章中,大多数发表于 2020 年(31 篇),更新了当前的主题。此外,2003 年至 2005 年期间有 10 篇文章发表,2011 年至 2015 年期间有 7 篇文章发表,反映了当时发生的疫情。与 CoV 类似,ZIKV 中大多数出版物也是在 2016 年至 2017 年爆发期间发表的(23 篇)。同样,大多数 CHIKV(13 篇)和 DENV(14 篇)出版物也发生在同一时间间隔内。EBOV(13 篇)和 MARV(4 篇)则发生在 2015 年至 2016 年之间。通过这篇综述,强调了几种可能在体内进化并在临床试验中用作这些病原体治疗方法的药物,表明瑞德西韦可能是一种对抗 CoV 的潜在治疗方法。此外,利巴韦林也可能是治疗 CHIKV 的潜在药物;索非布韦可能是治疗 ZIKV 的潜在药物;西福韦可能是治疗 DENV 的潜在药物,而法匹拉韦可能是对抗 EBOV 和 MARV 的潜在药物,为这些病原体的治疗带来了新的希望。
本文综述的结论表明了药物再利用策略在发现新药物方面的潜力,因为通过这种方法,药物可以用于治疗新兴的病毒性疾病。因此,该策略值得研究小组更多关注,是发现新兴病毒性疾病和其他疾病新药物的一种很有前途的方法。