Novel strategies are needed to make effective and safe vaccines against diseases such as AIDS, malaria, tuberculosis or hemorrhagic fevers. An approach that looks promising for challenging diseases like these is to deliver the vaccine into the body in a very safe and targeted way, using a ‘vehicle’ called a vector.
A vector is created by inserting gene segments encoding the parts of a pathogen that trigger an immune response (antigens) into a harmless virus. When this vector carrying the vaccine code is given to a person and enters the cells, it starts producing these antigens and presents them to the person’s immune system, which mounts its protective response against the real, disease-causing pathogen.
The vectors that have so far been shown to be best suited to the task of ‘gene taxi’ belong to the adenovirus family. This family of viruses is responsible for causing the common cold. Some members of the family are much more prevalent than others: for example, adenovirus serotype 5 (Ad5) is so common that most adults will have been exposed to it in childhood. Others are extremely rare. Crucell has pioneered the search for these very rare adenoviruses and their development as vectors. AdVac® technology encompasses these proprietary adenovirus vectors and all the expertise that Crucell has built up in this field.
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Crucell has developed a plasmid system that allows easy insertion of heterologous genes into the adenovirus serotype 11, 35 or 49 backbones. These plasmids, called pAdApt™/11, pAdApt™/35, or pAdApt™/49, together with relevant information regarding the restriction sites, are available under a MTA or license.