Researchers
test method for hantavirus, bioterror attack vaccines
Scientists
at the UNM School of Medicine Center for Emerging Infectious
Diseases have described and tested a new method for rapid vaccine
development that could dramatically speed and simplify the preparation
of future vaccines.
The centers
scientific leaders have long theorized that it should be possible
to prepare effective vaccines - even from germs that have never
been isolated or identified in the laboratory - using only tiny
gene fragments of a virus or bacterium freshly gathered from
the blood or tissues of an infected patient. To test that theory,
UNM investigators developed a rapid vaccine that
completely blocked infection with hantavirus in mice. This vaccine
is the first vaccine of any kind that has succeeded in blocking
the Sin Nombre hantavirus that has taken the lives of 26 New
Mexicans since its discovery in 1993.
After the
mailed anthrax attacks of last fall, scientists became increasingly
concerned about the prospect of further attacks by lethal viruses
such as hantaviruses, for which, unlike anthrax, there is no
effective treatment. In the modern era of genetic engineering,
bioterrorists could unleash pathogens for which there are no
vaccines or treatments, or those that have been deliberately
changed to evade existing vaccines.
The
threats posed by orphan germs that cause rare diseases
are especially serious, because it takes many years, even decades
to make a new vaccine by conventional means, said Brian
Hjelle, M.D., the centers director. One of the first
goals of UNMs Center for Emerging Infectious Diseases
has been to invent techniques that dramatically speed vaccine
development, such as in a setting of a rapidly-spreading bioterrorist
attack.
To test
whether they could develop a vaccine against a particularly
challenging organism, Hjelle and his colleagues chose the highly
lethal Sin Nombre virus, which kills 40 percent of its victims,
as the test organism. To test vaccine candidates using the live
hantavirus, the scientists infected deer mice.
The
advantage of using a hantavirus, according to investigator
Richard Lyons, M.D., Ph.D., is that so little is known
about the nature of vaccine protection against hantaviruses.
We can say that if this dramatically new technique for vaccination
works against hantaviruses, it will probably work against many
other pathogens, even if very little is known about the nature
of those organisms.
The UNM
investigators found that when deer mice were inoculated with
hantavirus and given a sham vaccine, all nine mice
became infected. Yet when the mice had been previously inoculated
with one of 10 new small pieces of the virus genetic material,
a strikingly high fraction, seven out of 10 vaccines, were able
to prevent infection in at least some deer mice. The investigators
were surprised to see that a full half of the vaccines, five
of the 10 vaccines, prevented infection in 75 percent or more
of the deer mice that were injected with hantavirus.
The
most exciting part of all was that so many fragments of the
virus DNA were effective vaccines in deer mice Hjelle
said. One fragment even blocked infection in 100 percent
of mice.
An article
describing their findings was recently published in the British
Journal of General Virology.
Other authors
on the paper include Mausumi Bharadwaj, Barbara Masten, Chunyan
Ye, Katy Mirowsky, Joyce Yee and Jason Botten.
The center
is supported by a grant from the federal Centers for Disease
Control and Prevention, an opportunity made available through
the efforts of New Mexico congresswoman Heather Wilson.