| Literature DB >> 28791258 |
Irfan A Rather1, Hilal A Parray2, Jameel B Lone2, Woon K Paek3, Jeongheui Lim3, Vivek K Bajpai1, Yong-Ha Park1.
Abstract
Dengue is currently the highest and rapidly spreading vector-borne viral disease, which can lead to mortality in its severe form. The globally endemic dengue poses as a public health and economic challenge that has been attempted to suppress though application of various prevention and control techniques. Therefore, broad spectrum techniques, that are efficient, cost-effective, and environmentally sustainable, are proposed and practiced in dengue-endemic regions. The development of vaccines and immunotherapies have introduced a new dimension for effective dengue control and prevention. Thus, the present study focuses on the preventive and control strategies that are currently employed to counter dengue. While traditional control strategies bring temporary sustainability alone, implementation of novel biotechnological interventions, such as sterile insect technique, paratransgenesis, and production of genetically modified vectors, has improved the efficacy of the traditional strategies. Although a large-scale vector control strategy can be limited, innovative vaccine candidates have provided evidence for promising dengue prevention measures. The use of tetravalent dengue vaccine (CYD-TDV) has been the most effective so far in treating dengue infections. Nonetheless, challenges and limitation hinder the progress of developing integrated intervention methods and vaccines; while the improvement in the latest techniques and vaccine formulation continues, one can hope for a future without the threat of dengue virus.Entities:
Keywords: dengue virus; disease; fever; infection; vaccine
Mesh:
Substances:
Year: 2017 PMID: 28791258 PMCID: PMC5524668 DOI: 10.3389/fcimb.2017.00336
Source DB: PubMed Journal: Front Cell Infect Microbiol ISSN: 2235-2988 Impact factor: 5.293
Figure 1Dengue virus infection.
Current Vaccine Candidates for Dengue Prevention (Source:Sandrasegaran, 2016).
| Live, attenuated chimeric (recombinant) | Acambis/Sanofi Pasteur | Insertion of genes coding for DENV structural proteins into a yellow fever virus (17D) backbone. | Phase III tetravalent—leading candidate |
| Centre for Disease Control (CDC)/Inviragen | Insertion of serotype genes into serotype II (DENV2- PDK53) DNA backbone. | Phase II monovalent | |
| National Institutes of Health (NIH)/University of Maryland | Insertion of serotype II and III genes into safer, more immunogenic serotype I and IV DNA backbone. Live attenuated DENV Delta-30 mutation | Phase I tetravalent | |
| Live, traditionally attenuated | Walter-Reed Army Institute of Research (WRAIR)/GlaxoSmithKline (GSK) | Attenuation achieved by growing the virus in cultured cells and selecting strains | Phase II tetravalent; technical issues |
| Mahidol Institute/Sanofi Pasteur | Phase II tetravalent | ||
| Inactivated | GSK | Viruses cultured and killed | Phase I tetravalent |
| Subunit | Hawaii Biotech | Viral immunogenic envelope is combined with viral non-structural protein antigens to produce recombinant 80% E subunit vaccine | Phase I tetravalent |
| DNA | WRAIR | Dengue prM-E DNA vaccine incorporating membrane and envelope genes into a plasmid vector | Phase I monovalent |