» Articles » PMID: 27525287

Dengue Fever: Causes, Complications, and Vaccine Strategies

Overview
Journal J Immunol Res
Publisher Wiley
Date 2016 Aug 16
PMID 27525287
Citations 104
Authors
Affiliations
Soon will be listed here.
Abstract

Dengue is a highly endemic infectious disease of the tropical countries and is rapidly becoming a global burden. It is caused by any of the 4 serotypes of dengue virus and is transmitted within humans through female Aedes mosquitoes. Dengue disease varies from mild fever to severe conditions of dengue hemorrhagic fever and shock syndrome. Globalization, increased air travel, and unplanned urbanization have led to increase in the rate of infection and helped dengue to expand its geographic and demographic distribution. Dengue vaccine development has been a challenging task due to the existence of four antigenically distinct dengue virus serotypes, each capable of eliciting cross-reactive and disease-enhancing antibody response against the remaining three serotypes. Recently, Sanofi Pasteur's chimeric live-attenuated dengue vaccine candidate has been approved in Mexico, Brazil, and Philippines for usage in adults between 9 and 45 years of age. The impact of its limited application to the public health system needs to be evaluated. Simultaneously, the restricted application of this vaccine candidate warrants continued efforts in developing a dengue vaccine candidate which is additionally efficacious for infants and naïve individuals. In this context, alternative strategies of developing a designed vaccine candidate which does not allow production of enhancing antibodies should be explored, as it may expand the umbrella of efficacy to include infants and naïve individuals.

Citing Articles

Immunologically effective biomaterials-enhanced vaccines against infection of pathogenic microorganisms.

Wei Q, Liu S, Huang X, Xin H, Ding J Biosaf Health. 2025; 5(1):45-61.

PMID: 40078604 PMC: 11894984. DOI: 10.1016/j.bsheal.2022.11.002.


Assessing the knowledge, attitudes, and practices (KAP) of dengue in Thailand: a systematic review and meta-analysis.

Crowley J, Liu B, Jan H Arch Public Health. 2025; 83(1):38.

PMID: 39953632 PMC: 11827231. DOI: 10.1186/s13690-025-01522-6.


Functional Verification of Differentially Expressed Genes Following DENV2 Infection in .

Chen X, Zhou X, Xie X, Li B, Zhao T, Yu H Viruses. 2025; 17(1).

PMID: 39861856 PMC: 11769442. DOI: 10.3390/v17010067.


Differential Transcriptional Landscape of Vero Cells During Dengue Virus 2 Infection in the Presence of Sinococuline.

Garg A, Shukla R, Kumar A, Aggarwal C, Mukhopadhyay A, Khanna N Microorganisms. 2025; 12(12.

PMID: 39770732 PMC: 11678108. DOI: 10.3390/microorganisms12122529.


Effective inhibition of dengue virus replication using 3'UTR-targeted Vivo-Morpholinos.

Niu M, Yi W, Dong Z, Li X, Dong X, Yu L Front Immunol. 2024; 15:1491230.

PMID: 39676860 PMC: 11638040. DOI: 10.3389/fimmu.2024.1491230.


References
1.
Perera R, Kuhn R . Structural proteomics of dengue virus. Curr Opin Microbiol. 2008; 11(4):369-77. PMC: 2581888. DOI: 10.1016/j.mib.2008.06.004. View

2.
Sun W, Cunningham D, Wasserman S, Perry J, Putnak J, Eckels K . Phase 2 clinical trial of three formulations of tetravalent live-attenuated dengue vaccine in flavivirus-naïve adults. Hum Vaccin. 2008; 5(1):33-40. DOI: 10.4161/hv.5.1.6348. View

3.
Kirkpatrick B, Whitehead S, Pierce K, Tibery C, Grier P, Hynes N . The live attenuated dengue vaccine TV003 elicits complete protection against dengue in a human challenge model. Sci Transl Med. 2016; 8(330):330ra36. DOI: 10.1126/scitranslmed.aaf1517. View

4.
Osorio J, Brewoo J, Silengo S, Arguello J, Moldovan I, Tary-Lehmann M . Efficacy of a tetravalent chimeric dengue vaccine (DENVax) in Cynomolgus macaques. Am J Trop Med Hyg. 2011; 84(6):978-87. PMC: 3110349. DOI: 10.4269/ajtmh.2011.10-0592. View

5.
Gubler D . Dengue/dengue haemorrhagic fever: history and current status. Novartis Found Symp. 2007; 277:3-16. DOI: 10.1002/0470058005.ch2. View