CAd3-ZEBOV: Difference between revisions
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{{Short description|A detailed overview of the CAd3-ZEBOV vaccine for Ebola virus}} | |||
== | ==Overview== | ||
CAd3-ZEBOV | [[File:Ebola_virus_em.png|thumb|right|Electron micrograph of the Ebola virus]] | ||
The '''CAd3-ZEBOV''' vaccine is a candidate vaccine developed to provide immunity against the [[Ebola virus]]. It is based on a recombinant [[chimpanzee adenovirus]] type 3 (CAd3) vector that expresses the [[glycoprotein]] of the [[Zaire ebolavirus]] (ZEBOV), which is responsible for the most severe outbreaks of [[Ebola virus disease]]. | |||
The vaccine | ==Development== | ||
The development of CAd3-ZEBOV was initiated in response to the urgent need for effective vaccines during the [[2014 West Africa Ebola outbreak]]. The vaccine was developed by the [[National Institute of Allergy and Infectious Diseases]] (NIAID) in collaboration with the pharmaceutical company [[GlaxoSmithKline]] (GSK). | |||
==Mechanism of Action== | |||
CAd3-ZEBOV utilizes a non-replicating viral vector to deliver the [[Ebola virus glycoprotein]] gene into the host cells. This induces an immune response by stimulating the production of [[antibodies]] and activating [[T-cells]], which are crucial for providing protection against the Ebola virus. | |||
==Clinical Trials== | ==Clinical Trials== | ||
[[File:Ebola_virus_em.png|thumb|left|Ebola virus particles]] | |||
The vaccine underwent several phases of clinical trials to evaluate its safety and efficacy. Initial trials demonstrated that CAd3-ZEBOV was well-tolerated and capable of eliciting a strong immune response in humans. Subsequent trials were conducted in [[West Africa]] during the Ebola outbreak to assess its effectiveness in preventing the disease. | |||
== | ==Challenges and Considerations== | ||
CAd3-ZEBOV | While CAd3-ZEBOV showed promise in early trials, challenges such as the logistics of vaccine distribution in outbreak settings and the need for cold chain storage were significant hurdles. Additionally, the emergence of new [[Ebola virus strains]] necessitates ongoing research and potential modifications to the vaccine. | ||
== | ==Related pages== | ||
* [[Ebola virus disease]] | * [[Ebola virus disease]] | ||
* [[Viral vector vaccine]] | * [[Viral vector vaccine]] | ||
* [[ | * [[Zaire ebolavirus]] | ||
* [[ | * [[2014 West Africa Ebola outbreak]] | ||
[[Category:Vaccines]] | [[Category:Vaccines]] | ||
[[Category:Ebola]] | [[Category:Ebola]] | ||
[[Category:Viral vaccines]] | [[Category:Viral vector vaccines]] | ||
Latest revision as of 03:31, 13 February 2025
A detailed overview of the CAd3-ZEBOV vaccine for Ebola virus
Overview[edit]

The CAd3-ZEBOV vaccine is a candidate vaccine developed to provide immunity against the Ebola virus. It is based on a recombinant chimpanzee adenovirus type 3 (CAd3) vector that expresses the glycoprotein of the Zaire ebolavirus (ZEBOV), which is responsible for the most severe outbreaks of Ebola virus disease.
Development[edit]
The development of CAd3-ZEBOV was initiated in response to the urgent need for effective vaccines during the 2014 West Africa Ebola outbreak. The vaccine was developed by the National Institute of Allergy and Infectious Diseases (NIAID) in collaboration with the pharmaceutical company GlaxoSmithKline (GSK).
Mechanism of Action[edit]
CAd3-ZEBOV utilizes a non-replicating viral vector to deliver the Ebola virus glycoprotein gene into the host cells. This induces an immune response by stimulating the production of antibodies and activating T-cells, which are crucial for providing protection against the Ebola virus.
Clinical Trials[edit]

The vaccine underwent several phases of clinical trials to evaluate its safety and efficacy. Initial trials demonstrated that CAd3-ZEBOV was well-tolerated and capable of eliciting a strong immune response in humans. Subsequent trials were conducted in West Africa during the Ebola outbreak to assess its effectiveness in preventing the disease.
Challenges and Considerations[edit]
While CAd3-ZEBOV showed promise in early trials, challenges such as the logistics of vaccine distribution in outbreak settings and the need for cold chain storage were significant hurdles. Additionally, the emergence of new Ebola virus strains necessitates ongoing research and potential modifications to the vaccine.