Guest guest Posted December 13, 1998 Report Share Posted December 13, 1998 Bad Medicine by Conrad A. Istock BULLETIN OF THE ATOMIC SCIENTISTS, NOV-DEC 1998, PP. 21-23 Anthrax vaccinations of U.S troops send a politically explosive message. They won't provide much protection, either. THE U.S. DEFENSE DEPARTMENT ANNOUNCED A YEAR ago that it would vaccinate all 2.4 million members of the U.S. armed forces against anthrax. Last August, the program got into high gear with the first large-scale vaccinations. Nonetheless, the anthrax vaccination program is a very bad idea—one whose time should never have come. The program will encourage and intensify several " biological arrns races. " It will also create new incentives for the manufacture and use of a wide variety of biological weapons. And it tells the world that the United States expects anthrax to be used in war, thereby eroding the force of the Biological Weapons Convention. Even in its primary purpose—protecting U.S. military personnel against anthrax in battle—it is certain to fail. I do not mean to suggest that anthrax is not a nasty weapon. Its destructive power was accurately portrayed by Defense Secretary Cohen, who explained that a quantity the size of a bag of sugar could kill half the people in Washington, D.C. It could produce victory in battle within a few days if unleashed on unprotected soldiers. But the biological, social, and political ramifications surrounding anthrax, or any other bioweapon. are far more complex than the Defense Department appears to realize. Although the military's vaccination program might seem like a wise precaution, it is in fact an ill-conceived idea likely to have a variety of unanticipated consequences—in short, a misadventure. To illustrate just one unpleasant consequence, consider the following scenario: Immunized U.S. troops are locked in combat. Suddenly, the enemv lays a cloud of anthrax spores over the entire battlefield. Within a few days. U.S. soldiers are dying in droves, but no enemy soldiers die. Why? Because the enemy did not release the particular strain of anthrax U.S. biologists used to make the vaccine. Instead, they used a strain specifically devised to defeat U.S. immunizations. This lethal strain had been developed years earlier by bioweaponeers in the former Soviet Union, using the U.S. vaccine as a tool in the search for a resistant strain. (The United States originally gave the vaccine to the Soviets for humanitarian purposes.) The resistant strain—and again this is strictly a hypothetical scenario—was secretly transferred to other countries, and the enemy soldiers were protected by specific immunization against the Soviet creation. THE BACTERIUM BACILLUS ANTHRACIS, THE SOURCE OF THE anthrax toxin, is easily grown in large quantities. It is also cultured to make vaccine. To use anthrax as a weapon, dry spores are mixed with an aerosol dispersant. Anthrax spores can lie dormant for decades. possiblv for centuries. Two extraordinary incidents attest to their durability. In 1942 British bioweaponeers carried out experiments with anthrax bombs on part of the island of Gruinard off the northwest coast of Scotland. Viable spores persisted for more than 40 years until the island was decontaminated in 1987 by literally soaking the soil with hundreds of thousands of liters of formaldehyde. Test data indicated that, without decontamination, viable spores would have persisted until at least 2050. Then there is the bizarre case of the sugar lumps laced with anthrax bacilli found in Baron Otto Karl von Rosen's luggage when he was arrested in Norway during World War I on suspicion of espionage and sabotage. The spores were in a liquid medium in tiny sealed capillarv tubes embedded in the sugar. Last year-- 80 vears later-- biologists at Britain’s Porton Down bioweapons detection center revived living colonies of the bacillus from the tube in the one lump of sugar tested. The genes for the anthrax toxin do not reside on the bacterium's main chromosome, but on a smaller, secondary DNA molecule called a plasmid. In laboratorv experiments these plasmids have been transferred from Bacillus anthracis to other species of bacteria. One transfer was to Bacillus thuringiensis, a bacterium widely used to control insects in gardens and in aerial spraying against gypsy moths. Another transfer was to a common soil bacterium, Bacillus cereus. The transfer of plasmids occurs naturally among many bacteria. Massive releases of anthrax spores could easilv lead, through the infection of animals, to spontaneous transfers of the plasmid to other bacteria as well. While anthrax does not spread from one human to another, it can propagate in the soil. In particular, its numbers increase in soils soaked with blood. And the spores from the soil can infect both humans and animals. Humans become infected by inhaling or swallowing spores, or by spores entering the body through cuts or scratches in the skin. Inhaling a clump of spores not much larger than a speck of dust can result in death. Anthrax is contracted most commonly by workers who handle wool, hides, or other materials from diseased animals. About 20 percent of untreated cases of cutaneous infection result in death. Ingested spores kill in 20 to 60 percent of cases; and 90 percent or more of those who become infected through inhalation die within a few days. The battlefield use of anthrax is plausible—more than a dozen countries have the weapon or are developing one, according to Pentagon officials. Until recently, laboratories could readily order anthrax cultures from U.S. suppliers. Before the Soviet Union abandoned its bioweapons program, Soviet scientists not only harvested anthrax spores in large quantity for use as a weapon, they also developed a highly effective dispersant that could quickly spread an invisible cloud of concentrated spores over a battlefield or a city. This dispersal technology may have been transferred to other countries. The United States also experimented with anthrax as a weapon. WOULD A VACCINATED POPULATION OF U.S SOLDIERS ON A battlefield be fully protected? If strains were used against which the immunization was completely effective, the answer would be " Yes, for a little while. " However, sending a large number of immunized individuals into contact with enormous numbers of bacteria would almost certainlv reveal spontaneous mutants against which the vaccine was no longer effective. An " evolutionary arms race " would begin, pitting the human ability to develop new vaccines against the microbes' ability to respond through natural selection—a bitter struggle we are all too familiar with in the case of newlv arising variants of flu viruses that repeatedly make previous flu vaccines obsolete. The same battle is occurring in the growing resistance of pathogenic bacteria to antibiotics. Based on animal testing, the U.S. vaccine does not offer protection against all strains of anthrax. In my scenario, an enemy used a strain known to break through that immunization. Thus, a " microbial-genetic arms race " would ensue in which newly developed strains rendered each previous vaccine useless. Either routine mutagenesis followed by selection, or genetic engineering, could be employed to produce resistant strains. No nation that produces bioweapons would be deterred by the Defense Department's use of a single vaccine. The microbial-genetic arms race could escalate wildly as potential combatants moved bevond anthrax to ever more deadly bacteria and viruses. Dozens of potential bioweapons exist—weapons based, for example, on the plague and Salmonella bacteria, or on the smallpox, dengue, encephalitis, and Ebola viruses. This would be a full-blown " pathogen-diversity arms race. " As nations interpret Defense’s program of immunizations as an invitation to dabble in bioweapons, the contest is likely to spiral. Could we attempt to vaccinate the entire U.S. military against every conceivable biological weapon? We cannot. There are no vaccines for many of these potential agents. Furthermore, some nations may interpret the Defense Department's move as a sign that the United States itself is considering using anthrax in war, thus creating the incentive to vaccinate their troops while developing their own alternative biological or chemical weapons. Were a large quantity of anthrax spores to be dispersed, the soil, vegetation, local animals, equipment, supplies, clothing, and personnel would be contaminated with dormant spores. Spores that adhere to objects or collect in recesses or on fabrics will readily become airborne again— and recalling Gruinard and the Baron's lumps of sugar, they will remain viable for a long time. At some future time, and in a non-battlefield location, unvaccinated people are likely to die after working with spore-laden equipment or other war materials returned to U.S. bases. Animals and unvaccinated people entering the contaminated battlefield are also likely to die—the biological analog of suffering caused by unexploded land mines. The numbers of post-war infections could be enormous. No human cases of anthrax have been reported in the United States (only five states have reported cases in animals), but returning troops would bring the disease home. The saddest of specters would be that of healthy men and women returning home from war, only to infect their own families and other unprotected civilians through contaminated duffel bags and other paraphernalia. Could the troops and their belongings come home after they had been exposed? Has the Defense Department thought about the decontamination procedures needed to make their return safe? THE UNITED STATES CURRENTLY HAS ABOUT SIX MlLLION doses of anthrax vaccine, according to Defense estimates. The Defense Department immunizations require six shots at two-week intervals, followed by three more at six, 12, and - 18 months, with annual booster shots thereafter. Vaccinating the military will require more than the present supply, and though more vaccine can be made fairly quickly, a large continuing supply will be required as new recruits enter the armed forces and booster shots are administered. It will be a major undertaking. If substantial numbers of the U.S. civilian population ever have to be protected against " bioterrorist " releases of anthrax, an enormous supply would be needed, with little guarantee that it could protect against the particular strain used by terrorists. We continue to live in a time of wars, with dangers from biological weapons probably now as great or greater than those from nuclear weapons. Biological weapons may pose a greater danger because they can be produced by " lowtech " methods, though this is somewhat less true as more and more genetic engineering is employed. These weapons can be nearly invisible. And if, unlike anthrax, contagious microbes are used as the basis for a weapon, they can create expanding epidemics—like a bomb that keeps on exploding. VACCINATING SERVICEMEN AND WOMEN WILL NOT EFFECTIVELY counter the threat of biological weapons. Instead, the Defense Department's initiative could erode the international strictures against the use of such weapons. If the 1972 Biological Weapons Convention is insufficient to prevent the production of biological weapons, then the 140 nations party to that treaty need to adopt verification procedures, including on-site inspections. This appears to be the solution toward which the U.N.’ s recent review conferences on the convention are moving. Treaty members should be urged onward until comprehensive inspections are a reality. Instead of encouraging perilous biological arms races, the United States should join with the United Nations to create stronger strictures and plans for immediate military reprisals that would send one clear message: " If you use a biological weapon once, it will be the last time. " Conrad A. Istock, a professor emeritus at the Department of Ecology and Evolutionary Biolog!y at the Universit!/ of Arizona, is a permanent visiting fellow in the Section of EcologIy and Systematics, Cornell University, Ithaca, New York. -- Meryl Nass, M.D. Parkview Hospital, Brunswick, Maine 04011 email mnass@... phone (207) 865-0875 fax (207) 865-6975 Quote Link to comment Share on other sites More sharing options...
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