Vaccination and antiviral treatment of neglected diseases caused by flaviviral infections
Autor: | K. Schleich, Cindy Nürnberger, Thomas Efferth, A. Sobanski |
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Rok vydání: | 2010 |
Předmět: |
Vaccines
Attenuated Biochemistry Antiviral Agents Virus Dengue fever Dengue Flaviviridae Drug Discovery Yellow Fever medicine Humans Encephalitis Japanese Pharmacology Attenuated vaccine biology Organic Chemistry Yellow fever Neglected Diseases Viral Vaccines Japanese encephalitis Flaviviridae Infections biology.organism_classification medicine.disease Virology Recombinant Proteins Vaccination Immunology Molecular Medicine Viral disease |
Zdroj: | Current medicinal chemistry. 18(4) |
ISSN: | 1875-533X |
Popis: | Flaviviral infections have a re-emerging impact on the health situation in developing countries with several billion of people living at risk. In the present review, we focus on three members of the genus Flavivirus belonging to the Flaviviridae family. They are transmitted to humans by mosquito bites, namely those viruses leading to Dengue Fever, Yellow Fever and mosquito-borne Japanese encephalitis. All three virus groups have a spherical structure with a diameter of approximately 50 nm. Although sharing a similar genomic structure and intracellular life cycle, they show different clinical manifestations. Infections are incurable, as there is no antiviral treatment available for either of the three viruses. Thus, prevention and vaccination are the best defenses. The most promising vaccines are live attenuated vaccines (LAVs), such as the YF17D strain against Yellow Fever or the SA-14-14-2 strain against Japanese encephalitis. Additionally, recombinant vaccines for Japanese encephalitis are in development. Although Dengue Fever is the most prevalent arthropode- borne flaviviral infection and a lot of research to develop a vaccine against all four Dengue Fever serotypes was undertaken, no vaccine is available on the market yet. Promising tetravalent vaccine candidates are currently undergoing clinical phase trials, including LAVs, recombinant and chimeric candidates as well as non-replicating vaccine approaches. Additionally, encouraging anti-flaviviral approaches target non-structural proteins, virus-specific proteases essential for cellular maturation of viral particles. Peptide inhibitors against the highly conserved NS2B and NS3 proteases are attractive as pan-flaviviral drug candidates. |
Databáze: | OpenAIRE |
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