To present short protein sequences to the host immune system a foreign
epitope has been expressed on the surface of the adenovirus virion as
part of the hexon. As the trimeric hexon constitutes 240 out of the 2
52 capsomers of the virus, the foreign epitope is repeated 720 times o
n the virion surface. An eight amino acid sequence from the major anti
genic site in the VP1 capsid protein of poliovirus type 3 was engineer
ed into two regions of the adenovirus type 2 hexon. The two loop regio
ns chosen to accommodate the foreign sequences are exposed on the surf
ace of the virion, show sequence variation between serotypes and are t
he sites of interaction with neutralizing antibodies. Virus with subst
itutions in loop I had wild-type growth characteristics, whereas virus
with substitutions in loop II grew poorly. Adenoviruses with poliovir
us sequences in loop I were recognized and efficiently neutralized by
antisera specific for the poliovirus sequence; an antiserum raised aga
inst the adenovirus with the poliovirus insert specifically recognized
the VP1 capsid protein of poliovirus type 3. It is therefore feasible
to alter the surface properties of the adenovirus virion and in doing
so to manipulate the immune response to this virus.