H2020Индивидуална стипендия2018–2020

FINDER · FIghtiNg DEngue viRus, a novel strategy for the development of fully protective antivirals that act by disrupting the DENV NS3/NS5 interaction

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период
2018-05-01 → 2020-04-30
Финансиране от ЕС
183 455 €
Участници
1
Схема
MSCA-IF-EF-ST

Линиите свързват координатора с партньорите.

Накратко на български

Вирусът Денге се изследва чрез търсене на молекули, които да блокират взаимодействието между протеините NS3 и NS5. Това е важно, за да се създадат нови противовирусни средства, които да намалят смъртността и тежките усложнения при заразените.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

FINDER: FIghtiNg DEngue viRus, a novel strategy for the development of fully protective antiviralsthat act by disrupting the DENV NS3/NS5 interaction

Dengue virus (DENV) is a virus transmitted by mosquitos that has spread to more than 130 countries in tropical and subtropical regions of the world. All four serologically different DENV are responsible for around 390 million infections, annually. While the majority of DENV infections cause a mild acute febrile illness called dengue, approximately 500,000 cases every year develop a severe dengue with potentially deadly consequences. Nearly half of the global population is currently exposed to the virus and due to global, environmental and economic factors (e.g. rising temperatures, increasing urbanization, and intercontinental travels), the frequency and the global distribution of DENV infections are expected to further grow in the future. Although DENV represents a major threat to global public health, no specific treatments or a fully protective and safe vaccine are available to treat and prevent DENV infections, highlighting the urgent need for developing new antiviral agents able to tackle this virus. The identification of molecules able to block specific and critical viral targets would clearly have an enormous impact on society. Indeed, antiviral drugs would dramatically decrease the global disease burden of dengue by essentially preventing the deadly complications and reducing the mortality rate of DENV infections. As a consequence, the availability of effective therapeutic options for DENV would also have a profound economic benefit as it will help to reduce the huge economic losses due to the costs incurred for hospitalisation and supportive care, mostly in low/middle-income countries. This project is focused on the early stages of the drug development and the main objective of FINDER is the development of innovative and effective anti-DENV therapeutic options able to disrupt the interaction between the viral NS3 and NS5 proteins, which play a key role in the viral replication. Since this target is highly conserved among the different DENV serotypes, the inhibition of this interaction by small molecules may represent a promising strategy for the development of drugs with efficacy against all DENV. Moreover, this class of compounds could be less prone to induce resistance as increasing evidence suggests that dissociative inhibitors of protein-protein interactions possess a high barrier to drug resistance. Overall, this project led to the identification of antiviral compounds acting by disrupting the NS3-NS5 interaction, paving the way for the development of a new class of selective anti-DENV agents.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Dengue virus (DENV) is the most prevalent arthropod-borne viral pathogen and infects about 400 million people worldwideevery year, causing epidemics that are spreading rapidly, with increased frequency and magnitude. To date, no specifictreatments or a fully protective vaccine are available for dengue. In line with the Priority 3 of H2020, the development ofeffective therapeutic strategies against DENV is urgently needed. The purpose of FINDER is that of developing innovativeanti-dengue candidate drugs able to disrupt the protein-protein interactions between the viral NS3 and NS5 proteins, two keyand conserved enzymes of DENV replication complex. To this end, some druggable cavities at the NS3/NS5 interface will beidentified and an in silico screening of a virtual small molecule library will be performed to search for potential inhibitors ofNS3/NS5 interaction. After the selection and the biological characterization of the hits, a hit-to-lead optimization step will becarried out to find compounds with lead-like properties. Such drugs are expected to be endowed with broad-spectrumantiviral activity, a reduced risk for developing resistance and lower undesirable side-effects. Through a comprehensivedissemination and exploitation strategy, one or more drug candidates will be evaluated in the future in animal models andthen in clinical trials. The outcomes of this project could fill the gap of the lack of effective anti-DENV drugs, resulting in anenormous impact on world-wide public health, as well as on the European competitiveness in this area. This project will alsocontribute to strengthen a wide set of skills of the applicant by a multidisciplinary training in the field of antiviral research,which will make him ready for attaining a position of independent researcher. In addition, the complementary competenciesbetween the applicant and the supervisor will allow a two-way transfer of knowledge, leading to a benefit also for the HostOrganisation.

Оригинален текст от CORDIS (на английски).

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Връзки

Данни: CORDIS, © Европейски съюз