In the past decade, adenovirus vectors have generated tremendous interest,
especially in gene therapy applications. In the so-called 'first generation
' adenovirus vectors, the transgenes are inserted in place of the El region
, or less often the E3 region. Although second-generation and helper-depend
ent adenovirus vectors will probably prevail in the future in applications
that require long-term gene expression, first generation adenovirus vectors
will remain very useful in other settings, such as cancer and vaccination,
or simply to transfect cell lines that are refractory to other transfectio
n methods. Until a few years ago, the construction of first generation aden
ovirus vectors was a labor-intensive and timeconsuming process. More than 2
0 methods have appeared that facilitate their construction and are reviewed
below.