» Articles » PMID: 31480297

Therapeutic Advances Against ZIKV: A Quick Response, a Long Way to Go

Overview
Publisher MDPI
Specialty Chemistry
Date 2019 Sep 5
PMID 31480297
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Zika virus (ZIKV) is a mosquito-borne flavivirus that spread throughout the American continent in 2015 causing considerable worldwide social and health alarm due to its association with ocular lesions and microcephaly in newborns, and Guillain-Barré syndrome (GBS) cases in adults. Nowadays, no licensed vaccines or antivirals are available against ZIKV, and thus, in this very short time, the scientific community has conducted enormous efforts to develop vaccines and antivirals. So that, different platforms (purified inactivated and live attenuated viruses, DNA and RNA nucleic acid based candidates, virus-like particles, subunit elements, and recombinant viruses) have been evaluated as vaccine candidates. Overall, these vaccines have shown the induction of vigorous humoral and cellular responses, the decrease of viremia and viral RNA levels in natural target organs, the prevention of vertical and sexual transmission, as well as that of ZIKV-associated malformations, and the protection of experimental animal models. Some of these vaccine candidates have already been assayed in clinical trials. Likewise, the search for antivirals have also been the focus of recent investigations, with dozens of compounds tested in cell culture and a few in animal models. Both direct acting antivirals (DAAs), directed to viral structural proteins and enzymes, and host acting antivirals (HAAs), directed to cellular factors affecting all steps of the viral life cycle (binding, entry, fusion, transcription, translation, replication, maturation, and egress), have been evaluated. It is expected that this huge collaborative effort will produce affordable and effective therapeutic and prophylactic tools to combat ZIKV and other related still unknown or nowadays neglected flaviviruses. Here, a comprehensive overview of the advances made in the development of therapeutic measures against ZIKV and the questions that still have to be faced are summarized.

Citing Articles

Crystallographic fragment screening and deep mutational scanning of Zika virus NS2B-NS3 protease enable development of resistance-resilient inhibitors.

von Delft F, Ni X, Richardson R, Godoy A, Ferla M, Kikawa C Res Sq. 2025; .

PMID: 39989958 PMC: 11844641. DOI: 10.21203/rs.3.rs-5876218/v1.


Evaluation of Thiazolidine Derivatives with Potential Anti-ZIKV Activity.

Goncalves S, Galdino L, Lima M, da Silva Moura J, Viana D, da Rosa M Curr Top Med Chem. 2024; 24(25):2224-2237.

PMID: 39136505 DOI: 10.2174/0115680266315388240801053401.


Crystallographic fragment screening and deep mutational scanning of Zika virus NS2B-NS3 protease enable development of resistance-resilient inhibitors.

Ni X, Richardson R, Godoy A, de Godoy A, Ferla M, Kikawa C bioRxiv. 2024; .

PMID: 38746305 PMC: 11092485. DOI: 10.1101/2024.04.29.591502.


Current Advances in Zika Vaccine Development.

Wang Y, Ling L, Zhang Z, Marin-Lopez A Vaccines (Basel). 2022; 10(11).

PMID: 36366325 PMC: 9694033. DOI: 10.3390/vaccines10111816.


Potential for Protein Kinase Pharmacological Regulation in Infections.

Blazquez A, Saiz J Int J Mol Sci. 2020; 21(24).

PMID: 33333737 PMC: 7765220. DOI: 10.3390/ijms21249524.


References
1.
Kumar A, Hou S, Airo A, Limonta D, Mancinelli V, Branton W . Zika virus inhibits type-I interferon production and downstream signaling. EMBO Rep. 2016; 17(12):1766-1775. PMC: 5283583. DOI: 10.15252/embr.201642627. View

2.
Palanichamy K, Joshi A, Mehmetoglu-Gurbuz T, Bravo M, Shlain M, Schiro F . Anti-Zika Activity of a Library of Synthetic Carbohydrate Receptors. J Med Chem. 2019; 62(8):4110-4119. DOI: 10.1021/acs.jmedchem.9b00142. View

3.
Snell N . Ribavirin--current status of a broad spectrum antiviral agent. Expert Opin Pharmacother. 2001; 2(8):1317-24. DOI: 10.1517/14656566.2.8.1317. View

4.
Varghese F, Rausalu K, Hakanen M, Saul S, Kummerer B, Susi P . Obatoclax Inhibits Alphavirus Membrane Fusion by Neutralizing the Acidic Environment of Endocytic Compartments. Antimicrob Agents Chemother. 2016; 61(3). PMC: 5328557. DOI: 10.1128/AAC.02227-16. View

5.
Mounce B, Cesaro T, Carrau L, Vallet T, Vignuzzi M . Curcumin inhibits Zika and chikungunya virus infection by inhibiting cell binding. Antiviral Res. 2017; 142:148-157. DOI: 10.1016/j.antiviral.2017.03.014. View