January 2006

Tobacco - The New Pharmacy

Enough anthrax vaccine to inoculate everyone in the United States could be grown inexpensively and safely with only one acre of tobacco plants, according to a molecular biologist at the University of Central Florida.  Mice immunized with a vaccine produced in UCF professor Henry Daniell’s laboratory through the genetic engineering of tobacco plants survived lethal doses of anthrax administered later by National Institutes of Health (NIH) researchers.  The results of the NIH-funded study are featured in the December issue of the Infection & Immunity journal.  Daniell’s research is a breakthrough in efforts to find a safe and effective method of producing large quantities of vaccine for anthrax, one of the top bioterrorism threats facing the United States.  The new production method also could help the government and health care providers avoid supply shortages, as one acre of plants can produce 360 million doses in a year.  “Anthrax vaccine is very much in need, primarily because of bioterrorism concerns,” Daniell said. “But in the United States, only one company has the capacity to produce the vaccine, and it is made in very small quantities by fermentation.  We can provide enough doses of a safe and effective vaccine for all Americans from just one acre of tobacco plants.” 

Current production of the vaccine involves an expensive fermentation process that can cause harmful side effects such as inflammation, flu-like symptoms and rashes.  This has prompted some people to refuse to be vaccinated.  The military now administers the vaccine with three shots in the first four weeks, three more in the next 17 months and then annual booster shots, according to the Pentagon.  Seeking a safer and more effective alternative, Daniell and his colleagues injected the vaccine gene into the chloroplast genome of tobacco cells, partly because of tobacco’s quick growth rate.  Tests showed the vaccine taken from the plants was just as potent as the one produced through fermentation but lacks the bacterial toxin that can cause harmful side effects.  Researchers then injected the vaccine into mice to immunize them against anthrax and sent the mice to NIH laboratories, where they survived doses of anthrax several times stronger than the amounts to which humans have been exposed. 

The next step for the anthrax vaccine would involve a company working with NIH to conduct clinical trials.  Human subjects would be injected only with the vaccine and not with anthrax itself, and scientists would then check the subjects’ immunity levels.  The vaccine later could be mass-produced and stockpiled for emergencies.  If that research is successful, the needs for requiring doctors to administer the shots and for shipping vaccines in refrigerated trucks, both of which can be especially difficult in poorer nations, would be eliminated.  Daniell conducted his study with part of a $1 million NIH grant and a $2 million U.S. Department of Agriculture grant that cover research related to genetic engineering in plants as a way to produce therapies for several diseases.  (UCF, 12/20/05). 

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