Through genetic engineering, scientists can isolate specific genes
and insert them into DNA of certain microbes or mammalian cells;
the microbes or cells become living factories, mass producing the
desired antigen. Then, using another product of biotechnology, a
monoclonal antibody that recognizes the antigen, the scientists
can separate the antigen from all the other material produced by
the microbe or cell. This technique has been used to produce immunogenic
but safe segments of the hepatitis B virus and the malaria parasite.
In
another approach, scientists have inserted genes for desired antigens
into the DNA of the vaccinia virus, the large cowpox virus familiar
for its role in smallpox immunization. When the reengineered vaccinia
virus is inoculated, it stimulates an immune reaction to both the
vaccinia and the products of its passenger genes. These have included,
in animal experiments, genes from the viruses that cause hepatitis
B, influenza, rabies, and AIDS.
Instead
of adding a gene, some scientists have snipped a key gene out of
an infectious organism. Thus crippled, the microbe can produce immunity
but not disease. This technique has been tried with a bacterium
that causes the severe diarrheal disease cholera; such a vaccine
is commercially available against a virus disease of pigs.
A
totally different approach to vaccine development lies in chemical
synthesis. Once scientists have isolated the gene that encodes an
antigen, they are able to determine the precise sequence of amino
acids that make up the antigen. They then pinpoint small key areas
on the large protein molecule, and assemble it chemical by chemical.
Wholly synthetic vaccines are being explored for malaria and for
the major diarrheal diseases that are so devastating in developing
countries.
Another
pioneering vaccine strategy exploits antiidiotype antibodies (see
A Web of Idiotypes). The original antibody (or idiotype) provokes
an antiantibody (or antiidiotype) that resembles the original antigen
on the disease-causing organism. The antiidiotype will not itself
cause disease, but it can serve as a mock antigen, inducing the
formation of antibodies that recognize and block the original antigen.
To make such a vaccine, scientists inject animals with a monoclonal
antibody (idiotype) against a disease-causing microorganism, then
harvest the antiidiotypes produced in response.