Antigen,
meet antibody
(continued)
Of
these, HTLV-1 is the least complicated. It's spread much like HIV
- by sexual contact, blood, breast milk, or sharing needles - but
it undergoes fewer mutations when it makes copies of itself. It
doesn't vary from person to person or even across inter- national
borders. HTLV-1 from St. Croix is very similar to HTLV-1 in Tokyo.
"That's
a big advantage," says Torres. "With vaccines for hepatitis
C or even influenza virus, variability is a problem - the viruses
constantly change. You make an antibody to one virus but that virus
turns into something else when it duplicates by changing key antigenic
properties."
"Because
HTLV-1 does not mutate as frequently as HIV, the antibodies that
the body generates in response to the virus have the potential to
work. With rapidly mutating viruses, you can develop a vaccine to
neutralize the virus, but the antibodies will only be effective
before the virus mutates."
The
virus-cancer connection has long been a source of scien- tific investigation.
Researchers have long known that retro- viruses can cause cancer
in animals. It was 1980 before the first human cancer/retrovirus
connection was established with the identification of HTLV-1.
Retroviruses
contain oncogenes that can be transferred during replication. They
can alter their host's chromosomes just enough to "switch on"
oncogenes that cause cells to grow out of control.
Top
right: To creat an HTLV-1 vaccine, researchers will harvest antibodies
from monkeys, who are also susceptible to the virus.
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