Drug intelligence / Profile preview

dengue tetravalent vaccine, live attenuated

Development stage
Approved
Lead developer
Sanofi
Modality
Vaccines & Immunotherapeutics
Administration
Subcutaneous
01

Overview

A **live attenuated tetravalent dengue vaccine** designed to prevent dengue disease caused by all four dengue virus serotypes (1, 2, 3, 4). Dengue tetravalent vaccines aim to provoke immune responses to all serotypes, minimizing the risk of severe dengue (including antibody-dependent enhancement). Several formulations exist: - **CYD-TDV (Dengvaxia)**, developed by recombinant DNA technology, is a chimeric vaccine using a yellow fever virus backbone expressing the prM and E proteins from each dengue serotype[1][3]. - **TAK-003**, developed by Takeda, is based on a live-attenuated DENV-2 backbone with prM/E genes from the other serotypes[4][5]. - **TV003/TV005**, developed by NIH, contains a mixture of live-attenuated viruses representing each serotype[3]. Mechanism of action: induces a broad, tetravalent immune response—priming neutralizing antibody and cellular immunity to all four dengue virus serotypes, preventing dengue infection and severe disease[1][3][4]. Indications: Prevention of dengue disease in individuals with prior dengue infection (for CYD-TDV/Dengvaxia); indications for other formulations may include naïve individuals (e.g., TAK-003 has demonstrated protection regardless of baseline serostatus in clinical trials).

Brand names
DengvaxiaQdenga
Other names
dengue tetravalent vaccine, livelive attenuated dengue vaccine
02

Targets

Dengue virus nonstructural proteinsC protein (Dengue virus capsid protein)

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